﻿<?xml version="1.0" encoding="utf-8"?><rss version="2.0"><channel><title>Labslink Research News</title><link>http://www.labslink.com</link><description>The latest research news from labslink.com.</description><copyright>Copyright 2009 Labslink.com. All rights reserved.</copyright><image><url>http://www.labslink.com/images/logo.gif</url><title>Labslink.com</title><link>http://www.labslink.com</link></image><item><title>Women's reproductive ability may be related to immune system status</title><description>New research  indicates that women&amp;rsquo;s reproductive function may be tied  to their immune  status. Previous studies have found this association in  human males, but not  females........&amp;gt;&lt;a href="http://news.illinois.edu/news/13/0517reproduction_immunity_KathrynClancy.html" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9474</link><pubDate>Fri, 17 May 2013 14:27:59 PDT</pubDate></item><item><title>Guelph scientists develop first vaccine to help control autism symptoms</title><description>A first-ever vaccine created by University of Guelph researchers for gut  bacteria common in autistic children may also help control some autism  symptoms.......&amp;gt;&lt;a href="http://www.uoguelph.ca/news/2013/04/guelph_scientis_1.html" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9403</link><pubDate>Wed, 24 Apr 2013 16:14:23 PDT</pubDate></item><item><title>Study: Research reveals protective properties of influenza vaccines</title><description>Collaborating scientists from Nationwide Children&amp;rsquo;s Hospital,  Baylor Institute for Immunology Research, and Mount Sinai School of  Medicine have identified an important mechanism for stimulating  protective immune responses following seasonal influenza vaccinations.  The study was published in &lt;em&gt;Science Translational Medicine&lt;/em&gt;, a journal of the American Association for the Advancement of Science (AAAS)........&amp;gt; &lt;a href="http://www.nationwidechildrens.org/news-room-articles/study-research-reveals-protective-properties-of-influenza-vaccines?contentid=115127" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9302</link><pubDate>Mon, 25 Mar 2013 16:24:38 PDT</pubDate></item><item><title>Target Meeting’s 2nd World Immunology Online Conference, March 19-21, 2013: Join For Free</title><description>A Free Virtual &lt;span class="st_tag internal_tag"&gt;Immunology&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;/span&gt;&lt;/span&gt;&lt;span class="st_tag internal_tag"&gt;Conference&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;/span&gt;&lt;/span&gt;at Targetmeeting.com featuring 60+ live presentations (12 sessions)  from academic and industry experts around the world. Computer and  internet connection are required but no special equipment or software  needed. All the attendees just connect to the &lt;span class="st_tag internal_tag"&gt;online conference&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;span class="chicklets tag internal_tag"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&amp;rsquo;s  server to participate in real time with their distinguished  counterparts from across the globe. They can participate from their home  or office depending on their convenience. Furthermore, attendees can  earn the free Certificates of Attendance. It is a great opportunity to  learn about recent advances in the field of &lt;span class="st_tag internal_tag"&gt;immunology&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;span class="chicklets tag internal_tag"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt; without travel and money cost.
Major Sessions Includes:
&lt;ul&gt;
&lt;li&gt;Cancer and immunology Immune regulation &lt;/li&gt;
&lt;li&gt;Vaccine development &lt;/li&gt;
&lt;li&gt;Immunity disease molecular mechanisms Infection and immunity &lt;/li&gt;
&lt;li&gt;Immunotherapy&lt;/li&gt;
&lt;li&gt;And many more&amp;hellip;&lt;/li&gt;
&lt;/ul&gt;
Researchers, medical professionals, and other related people can enjoy many benefits by participating in the &lt;span class="st_tag internal_tag"&gt;2nd World Immunology&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;span class="chicklets tag internal_tag"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt; Online Conference. They can know, learn and follow up on major  developments taking place in the areas of interest. You can have the  rare privilege of meeting the best international speakers and  world-renowned researchers in real time. You can have that much-needed  opportunity of networking and exchanging views with the target audience  directly.
Participants get a worldwide platform to express their  opinions and ideas. With their experience and expertise, they can build  a solid reputation and create a tremendous and lasting impact on the  community. The &lt;span class="st_tag internal_tag"&gt;2nd World&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;span class="chicklets tag internal_tag"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt; Immunology Online Conference can create new opportunities for the  leading life science professionals and can help them establish new  associations with fellow researchers.
According to &lt;span class="st_tag internal_tag"&gt;Target Meeting&lt;span class="stButton" style="text-decoration: none; color: #000000; display: inline-block; cursor: pointer; padding-left: 0px; padding-right: 0px; width: 16px;"&gt;&lt;span class="chicklets tag internal_tag"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;,  all presentations and discussions happen in real time. Importantly,  they save the participants the hassle of travel; help them use their  valuable time effectively and save money. Participants can ask  questions, discuss problems, and exchange their ideas on the online  platform. The conference presents them the ultimate opportunity to  discuss their proposals and initiatives with global experts, something  that perhaps would not have been possible using other methods of  communication or correspondence.
Target Meeting is a leading  online life science conference organizer. Thousands of international  speakers and ten thousands of attendees participated in the online  symposiums and conferences at Target Meeting. With the persistent  efforts, Target Meeting has achieved a well-respected reputation among  the attendees and within life science communities, based on the quality  of organizers, speakers and scientific programs, as well as excellent  attendee experience. They have a solid record of having created  outstanding opportunities for scientists and clinicians to share their  latest research and in inspiring breakthrough ideas. The conferences are  a great way to establish and maintain professional relationships with  the best brains in medical science.
Sign up early (free) to secure your place, please visit http://www.targetmeeting.com.
Upcoming Free Online Conferences at Target Meeting include:
&lt;ul&gt;
&lt;li&gt;March 19-21, 2013, TM&amp;rsquo;s 2nd world immunology online conference.&lt;/li&gt;
&lt;li&gt;April 16-18, 2013, TM&amp;rsquo;s 2nd world virology &amp;amp; microbiology online conference.&amp;acirc;&amp;euro;&amp;uml;&lt;/li&gt;
&lt;li&gt;May 21-23, 2013, TM&amp;rsquo;s 2nd world genetics &amp;amp; genomics online conference.&lt;/li&gt;
&lt;li&gt;June 18-20, 2013, TM&amp;rsquo;s 2nd world neuroscience online conference.&amp;acirc;&amp;euro;&amp;uml;&lt;/li&gt;
&lt;/ul&gt;
Contact: &lt;br /&gt; William Smith&lt;br /&gt; Target Meeting&lt;br /&gt; Williams @ targetmeeting dot com&lt;br /&gt;&amp;acirc;&amp;euro;&amp;uml;Belliare, TX, 77401, USA</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9272</link><pubDate>Sun, 17 Mar 2013 17:23:21 PDT</pubDate></item><item><title>UTSW researchers identify new enzyme that acts as innate immunity sensor</title><description>Two studies by researchers at UT Southwestern Medical Center could lead  to new treatments for lupus and other autoimmune diseases and strengthen  current therapies for viral, bacterial, and parasitic infections........&amp;gt;&lt;a href="http://www.utsouthwestern.edu/newsroom/news-releases/year-2013/feb/dna-defense-chen.html" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=9189</link><pubDate>Fri, 15 Feb 2013 17:39:59 PDT</pubDate></item><item><title>New research helps predict susceptibility to Burkitt lymphoma</title><description>New research, presented this morning at the 54th Annual Meeting of the  American Society of Hematology (ASH), has identified important  associations between &lt;em&gt;Plasmodium falciparum&lt;/em&gt; &amp;nbsp;(&lt;em&gt;Pf&lt;/em&gt;) malaria and endemic Burkitt Lymphoma (eBL) that may help researchers identify young children who are more susceptible to eBL........&amp;gt; &lt;a href="http://www.gwumc.edu/news/newsitems.cfm?neID=921&amp;amp;account=SMHS" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8924</link><pubDate>Tue, 11 Dec 2012 16:20:06 PDT</pubDate></item><item><title>Genes and immune system shaped by childhood poverty, stress</title><description>A University of British Columbia and Centre for Molecular Medicine and Therapeutics (CMMT) study has revealed that childhood poverty, stress as an adult,  and demographics such as age, sex and ethnicity, all leave an imprint on  a person&amp;rsquo;s genes. And, that this imprint could play a role in our  immune response.........&amp;gt; &lt;a href="http://www.publicaffairs.ubc.ca/2012/10/18/genes-and-immune-system-shaped-by-childhood-poverty-stress/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8781</link><pubDate>Sat, 20 Oct 2012 19:35:20 PDT</pubDate></item><item><title>No antibodies, no problem</title><description>Researchers at the Johns Hopkins Bloomberg School of Public Health have  determined a new mechanism by which the mosquitoes&amp;rsquo; immune system can  respond with specificity to infections with various pathogens, including  the parasite that causes malaria in humans, using one single gene.......&amp;gt; &lt;a href="http://www.jhsph.edu/news/news-releases/2012/dimopoulos_antibiodies.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8775</link><pubDate>Thu, 18 Oct 2012 14:19:03 PDT</pubDate></item><item><title>Duke Medicine news -- Anti-cancer drug fights immune reaction in some infants with Pompe disease</title><description>A simplified, conceptual diagram of a humoral immune response to a  therapeutic protein and targets of various immunomodulatory agents.  Immune modulation with rituximab.......&amp;gt; &lt;a href="http://www.dukehealth.org/pompe-disease-graphic" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8750</link><pubDate>Thu, 11 Oct 2012 16:26:08 PDT</pubDate></item><item><title>Feeding microbials to chickens leads to mysterious immune response</title><description>Researchers at the North Carolina State University and Chung Jen College  of Nursing, Health Sciences and Management (Taiwan) conducted a study  to investigate the effects of direct fed microbials on energy metabolism  in different tissues of broiler chickens. The researchers wanted to  learn how consuming microbials and probiotics could change energy use  and immune function. Typically, direct fed microbials and probiotics are  used to improve livestock health, but how they actually work is not  fully understood........&amp;gt; &lt;a href="http://asas.org/about-asas/press-room/interpretive-summary-archive/feeding-microbials-to-chickens-leads-to-mysterious-immune-response" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8700</link><pubDate>Wed, 12 Sep 2012 12:40:11 PDT</pubDate></item><item><title>Behind closed doors: Researchers show how probiotics boost plant immunity</title><description>With the help of beneficial bacteria, plants can slam the door when  disease pathogens come knocking, University of Delaware researchers have  discovered........&amp;gt; &lt;a href="http://www.udel.edu/udaily/2013/aug/beneficial-soil-bacteria-082712.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8647</link><pubDate>Mon, 27 Aug 2012 15:01:20 PDT</pubDate></item><item><title>SIgN scientists discover dendritic cells key to activating human immune responses</title><description>&lt;span id="dnn_ctr1561_ContentPane" class="DNNAlignleft"&gt;&lt;span class="Normal"&gt;&lt;span&gt;&lt;span&gt;Scientists  at A*STAR&amp;rsquo;s Singapore Immunology Network (SIgN), in collaboration with  Newcastle University, UK, the Singapore Institute of Clinical Sciences  and clinicians from multiple hospitals &lt;/span&gt;&lt;/span&gt;&lt;span&gt;in Singapore, have identified a new&lt;span&gt; &lt;span&gt;subset of dendritic cells (DCs) in human peripheral tissue which have a critical role in activating our immune........&amp;gt; &lt;a href="http://www.a-star.edu.sg/Media/News/PressReleases/tabid/828/articleType/ArticleView/articleId/1675/Default.aspx" target="_blank"&gt;Full story&lt;/a&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8507</link><pubDate>Mon, 16 Jul 2012 18:03:33 PDT</pubDate></item><item><title>Programmable DNA scissors found for bacterial immune system</title><description>Genetic engineers and genomics researchers should welcome the news from  the Lawrence Berkeley National Laboratory (Berkeley Lab) where an  international team of scientists has discovered a new and possibly more  effective means of editing genomes. This discovery holds potentially big  implications for advanced biofuels and therapeutic drugs.......&amp;gt; &lt;a href="http://newscenter.lbl.gov/feature-stories/2012/06/28/programmable-dna-scissors/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8458</link><pubDate>Thu, 28 Jun 2012 18:05:55 PDT</pubDate></item><item><title>UGA study reveals flu-fighting role for well-known immune component</title><description>University of Georgia scientists have discovered a new flu-fighting role  for a well-known component of the immune system. Kimberly Klonowski,  assistant professor of cellular biology in the UGA Franklin College of  Arts and Sciences, and her colleagues found that administering a  cell-signaling protein known as IL-15 to mice infected with influenza  reduces their peak viral load by nearly three times........&amp;gt; &lt;a href="http://news.uga.edu/releases/article/flu-fighting-role-for-immune-component-062612/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8451</link><pubDate>Tue, 26 Jun 2012 19:39:49 PDT</pubDate></item><item><title>Moffitt researcher, colleagues find success with new immune approach to fighting some cancers</title><description>A national research collaboration of senior researchers, including a researcher from Moffitt Cancer Center,  has found that 20 to 25 percent of "heavily pre-treated" patients with a  variety of cancers who enrolled in a clinical trial had "objective and  durable" responses to a treatment with BMS-936558, an antibody that  specifically blocks programmed cell death 1 (PD-1).&amp;nbsp; PD-1 is a key  immune "checkpoint" receptor expressed by activated immune cells  (T-cells) and is involved in the suppression of immunity........&amp;gt; &lt;a href="http://www.insidemoffitt.com/content.cfm?page_id=392&amp;amp;press_release_id=533" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8430</link><pubDate>Wed, 13 Jun 2012 17:45:17 PDT</pubDate></item><item><title>Moffitt Cancer Center researchers develop and test new anti-cancer vaccine</title><description>Researchers at Moffitt Cancer Center have developed and tested in mice a synthetic vaccine and found it  effective in killing human papillomavirus-derived cancer, a virus linked  to cervical cancers among others.&amp;nbsp; The research was published in a recent issue of Cancer Immunology, Immunotherapy........&amp;gt; &lt;a href="http://www.insidemoffitt.com/content.cfm?page_id=392&amp;amp;press_release_id=528" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8415</link><pubDate>Fri, 08 Jun 2012 16:53:58 PDT</pubDate></item><item><title>An important breakthrough in immunology by IRCM researchers</title><description>A team of researchers at the IRCM led by &lt;strong style="font-size: 13px;"&gt;Dr. Andr&amp;eacute; Veillette &lt;/strong&gt;made an important breakthrough in the field of immunology, which will be published online today by the scientific journal &lt;em style="font-size: 13px;"&gt;Immunity......&amp;gt; &lt;a href="http://www.ircm.qc.ca/Medias/Communiques/Pages/detail.aspx?pID=61&amp;amp;PFLG=1033" target="_blank"&gt;Full story&lt;/a&gt;&lt;br /&gt;&lt;/em&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8412</link><pubDate>Thu, 07 Jun 2012 17:06:39 PDT</pubDate></item><item><title>New technology improves malaria control and vaccine development</title><description>A new technique that accurately determines the risk of infants in  endemic countries developing clinical malaria could provide a valuable  tool for evaluating new malaria prevention strategies and vaccines.
The technique could even help to understand how anti-malarial vaccine and treatment strategies act to reduce malaria.......&amp;gt; &lt;a href="http://www.wehi.edu.au/site/latest_news/new_technology_improves_malaria_control_and_vaccine_development" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8406</link><pubDate>Tue, 05 Jun 2012 17:09:44 PDT</pubDate></item><item><title>Vitamin D + TB vaccine: Allies in fight against bladder cancer?</title><description>The tuberculosis vaccine is often used as a treatment for bladder  cancer, and adding vitamin D might improve the vaccine&amp;rsquo;s effectiveness,  according to new research from the University of Rochester Medical Center presented today at the American Urological Association annual meeting........&amp;gt; &lt;a href="http://www.urmc.rochester.edu/news/story/index.cfm?id=3513" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8360</link><pubDate>Mon, 21 May 2012 17:04:43 PDT</pubDate></item><item><title>Regulatory immune cell diversity tempers autoimmunity in rheumatoid arthritis</title><description>Untangling the root cause of rheumatoid arthritis has been a difficult  task for immunologists, as decades of research has pointed to multiple  culprits in our immune system, with contradictory lines of evidence.  Now, researchers at The Wistar Institute announce that it takes a  diverse array of regulatory T cells (a specialized subset of white blood  cells) to prevent the immune system from generating the tissue-specific  inflammation that is a hallmark of the disease........&amp;gt; &lt;a href="http://wistar.org/news-and-media/press-releases/regulatory-immune-cell-diversity-tempers-autoimmunity-rheumatoid-arthr" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8338</link><pubDate>Tue, 08 May 2012 17:03:27 PDT</pubDate></item><item><title>Salmonella infection, but not as we know it</title><description>Salmonella is an important bacterium to study as it causes a range of  diseases in humans and animals. It is capable of growing and reproducing  inside macrophages - a type of white blood cell that ingests foreign  material - ultimately destroying them. These macrophage cells are key  players in the immune response to invaders and so the control of  Salmonella within these cells is critical to surviving an infection........&amp;gt; &lt;a href="http://www.bbsrc.ac.uk/news/health/2012/120425-pr-salmonella-infection.aspx" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8311</link><pubDate>Wed, 25 Apr 2012 17:30:55 PDT</pubDate></item><item><title>New genetic mechanism of immune deficiency discovered</title><description>Researchers at National Jewish Health have discovered a novel genetic mechanism of immune deficiency. Magdalena M. Gorska, MD, PhD, and Rafeul Alam, MD, PhD, identified a mutation in Unc119 that causes immunodeficiency&amp;nbsp; known as idiopathic CD4 lymphopenia........&amp;gt; &lt;a href="http://www.nationaljewish.org/about/mediacenter/pressreleases/2012/unc119/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8299</link><pubDate>Fri, 20 Apr 2012 16:32:05 PDT</pubDate></item><item><title>The long arm of the dendritic cell</title><description>Atherosclerosis is a major cause of death in Western societies. The  illness is due to the formation of insoluble deposits called  atherosclerotic plaques on the walls of major arteries as a consequence  of chronic, localized inflammation reactions. By reducing blood flow,  the plaques can provoke heart attacks and strokes. A class of immune  cells called dendritic cells plays a crucial role in facilitating the  development of these plaques........&amp;gt; &lt;a href="http://www.en.uni-muenchen.de/news/newsarchiv/2012/2012_doering.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8268</link><pubDate>Wed, 04 Apr 2012 17:09:48 PDT</pubDate></item><item><title>A*STAR scientists discover special class of natural fats stimulates immune cells to fight diseases</title><description>&lt;span id="dnn_ctr1561_ContentPane" class="DNNAlignleft"&gt;&lt;span class="Normal"&gt;An  international research team led by scientists from Singapore Immunology  Network (SIgN) under the Agency of Science, Technology and Research  (A*STAR) discovered that a special class of fatty molecules is essential  for activating a unique group of early-responding immune cells. This  study sheds light on how recognition of fatty molecules by immune cells  could protect from infection........&amp;gt; &lt;a href="http://www.a-star.edu.sg/Media/News/PressReleases/tabid/828/articleType/ArticleView/articleId/1622/Default.aspx" target="_blank"&gt;Full story&lt;/a&gt;&lt;br /&gt;&lt;/span&gt;&lt;/span&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8258</link><pubDate>Mon, 02 Apr 2012 17:06:28 PDT</pubDate></item><item><title>A 24-karat gold key to unlock the immune system</title><description>Developing a drug or vaccine requires a delicate balancing act with the  immune system. On one hand, medications need to escape detection by the  immune system in order to perform their function. But vaccinations &amp;mdash;  de-activated versions of a disease or virus &amp;mdash; need to do the reverse.  They prompt the immune system to create protective antibodies. But  scientists are still stumped by how the immune system recognizes  different particles, and how it chooses whether or not to react against  them.......&amp;gt; &lt;a href="http://www.aftau.org/site/News2?page=NewsArticle&amp;amp;id=16323" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8246</link><pubDate>Mon, 26 Mar 2012 17:31:19 PDT</pubDate></item><item><title>Immune system implicated in prematurity complication</title><description>Despite advances in neonatal care, necrotizing enterocolitis (NEC) &amp;ndash; the  most common gastrointestinal emergency in premature infants &amp;ndash; continues  to be a deadly disease........&amp;gt;&lt;a href="http://www.mc.vanderbilt.edu/reporter/index.html?ID=12359" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8226</link><pubDate>Mon, 19 Mar 2012 16:45:31 PDT</pubDate></item><item><title>Depression could be evolutionary byproduct of immune system</title><description>Depression is common enough &amp;ndash; afflicting one in ten adults in the United States -- that it seems the possibility of depression  must be &amp;ldquo;hard-wired&amp;rdquo; into our brains. This has led biologists to propose  several theories to account for how depression, or behaviors linked to  it, can somehow offer an evolutionary advantage.......&amp;gt; &lt;a href="http://news.emory.edu/stories/2012/02/depression_evolution/campus.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8175</link><pubDate>Thu, 01 Mar 2012 16:26:35 PDT</pubDate></item><item><title>'Universal' vaccines could finally allow for wide-scale flu prevention</title><description>An emerging class of long-lasting flu vaccines could do more than just save people the trouble of an annual flu shot. Princeton University-based researchers have found that the  "universal" vaccine could for the first time allow for the effective,  wide-scale prevention of flu by limiting the influenza virus' ability to  spread and mutate. Universal, or cross-protective, vaccines &amp;mdash; so named  for their effectiveness against several flu strains &amp;mdash; are being  developed in various labs worldwide and some are already in clinical  trials.......&amp;gt; &lt;a href="http://www.princeton.edu/main/news/archive/S33/01/19A05/" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8162</link><pubDate>Mon, 27 Feb 2012 17:00:40 PDT</pubDate></item><item><title>SIV infection may lead to increase in immune-suppressive Treg cells</title><description>Tissue in monkeys infected with a close relative of HIV can ramp up  production of a type of T cell that actually weakens the body's attack  against the invading virus. The discovery, in lymph nodes draining the  intestinal tract, could help explain how the HIV virus evades the body's  immune defenses.......&amp;gt; &lt;a href="http://www.ucdmc.ucdavis.edu/publish/news/newsroom/6238" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8126</link><pubDate>Tue, 14 Feb 2012 17:10:28 PDT</pubDate></item><item><title>Sensing self and non-self: New research into immune tolerance</title><description>t the most basic level, the immune system must distinguish self from  non-self, that is, it must discriminate between the molecular signatures  of invading pathogens (non-self antigens) and cellular constituents  that usually pose no risk to health (self-antigens)........&amp;gt; &lt;a href="http://www.biodesign.asu.edu/news/sensing-self-and-non-self-new-research-into-immune-tolerance" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8122</link><pubDate>Mon, 13 Feb 2012 16:37:43 PDT</pubDate></item><item><title>Secrets of immune response illuminated in new study</title><description>When disease-causing invaders like bacteria infect a human host,  cells of various types swing into action, coordinating their activities  to address the threat. In new research appearing in this month&amp;rsquo;s issue of  the journal Nature Immunology, Roy Curtiss, director of the Center for  Infectious Diseases and Vaccinology at the Biodesign Institute at  Arizona State University, along with international collaborators,  investigates the coordination of a particular type of immune response,  involving the release of of IFN-&amp;lambda;&amp;mdash; a cell-signaling protein molecule  known as a cytokine........&amp;gt; &lt;a href="http://biodesign.asu.edu/news/secrets-of-immune-response-illuminated-in-new-study" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8111</link><pubDate>Thu, 09 Feb 2012 17:37:22 PDT</pubDate></item><item><title>UT MD Anderson, Texas A&amp;M team up to treat canine lymphoma</title><description>A new immunotherapy for companion dogs with advanced-stage non-Hodgkin  lymphoma (NHL) has been shown to improve survival while maintaining  quality of life, according to a study published in the journal Scientific Reports. The study resulted from a collaboration between The University of Texas MD Anderson Children&amp;rsquo;s Cancer Hospital in Houston and Texas A&amp;amp;M University College of Veterinary Medicine in College Station.......&amp;gt; &lt;a href="http://www.mdanderson.org/newsroom/news-releases/2012/canine-lymphoma.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8101</link><pubDate>Tue, 07 Feb 2012 19:01:22 PDT</pubDate></item><item><title>Aiding cancer therapy by mathematically modeling tumor-immune interactions</title><description>Cancer is one of the five leading causes of death. And yet, despite  decades of research, there is no standardized first-line treatment for  most cancers. In addition, disappointing results from predominant  second-line treatments like chemotherapy have established the need for  alternative methods.......&amp;gt; &lt;a href="http://connect.siam.org/?p=1628" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8057</link><pubDate>Wed, 25 Jan 2012 18:32:42 PDT</pubDate></item><item><title>Penn researchers help solve questions about Ethiopians' high-altitude adaptations</title><description>Over many generations, people living in the high-altitude regions of the  Andes or on the Tibetan Plateau have adapted to life in low-oxygen  conditions. Living with such a distinct and powerful selective pressure  has made these populations a textbook example of evolution in action,  but exactly how their genes convey a survival advantage remains an open  question........&amp;gt; &lt;a href="http://www.upenn.edu/pennnews/news/penn-researchers-help-solve-questions-about-ethiopians-high-altitude-adaptations" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8044</link><pubDate>Fri, 20 Jan 2012 17:10:26 PDT</pubDate></item><item><title>Many high-risk Americans don't get hepatitis B vaccine</title><description>Although there is an effective vaccine for hepatitis B and public health  officials have a strong sense of who is at highest risk for the  infectious liver disease, tens of thousands of people in the United  States contract the virus every year. According to a new study by  researchers at Brown University, missed opportunities to administer the  vaccine continue to be a reason why infections persist........&amp;gt; &lt;a href="http://news.brown.edu/pressreleases/2012/01/hepatitisb" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8039</link><pubDate>Thu, 19 Jan 2012 17:16:08 PDT</pubDate></item><item><title>Researchers find new, noninvasive way to identify lymph node metastasis</title><description>Using two cell surface markers found to be highly expressed in breast cancer lymph node metastases, researchers at Moffitt Cancer Center,  working with colleagues at other institutions, have developed targeted,  fluorescent molecular imaging probes that can non-invasively detect  breast cancer lymph node metastases. The new procedure could spare  breast cancer patients invasive and unreliable sentinel lymph node (SLN)  biopsies and surgery-associated negative side effects.......&amp;gt;&lt;a href="http://www.insidemoffitt.com/content.cfm?page_id=392&amp;amp;press_release_id=468" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=8023</link><pubDate>Fri, 13 Jan 2012 17:38:52 PDT</pubDate></item><item><title>Research shows progress toward a genital herpes vaccine</title><description>An investigational vaccine protected some women against infection from  one of the two types of herpes simplex viruses that cause genital  herpes, according to findings in the &lt;em&gt;New England Journal of Medicine&lt;/em&gt;........&amp;gt; &lt;a href="http://www.slu.edu/x57441.xml" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7983</link><pubDate>Wed, 04 Jan 2012 17:14:18 PDT</pubDate></item><item><title>Cobblestones fool innate immunity</title><description>Activation of the body&amp;rsquo;s innate immune system is one of the most common  reasons for an implant being rejected,&amp;rdquo; explains Professor Hans Elwing  from the University of Gothenburg&amp;rsquo;s Department of Cell and Molecular  Biology. &amp;ldquo;We can now show why the body more easily integrates implants  with a nanostructured surface than a smooth one........&amp;gt; &lt;a href="http://www.science.gu.se/english/News/News_detail/?languageId=100001&amp;amp;contentId=1050011&amp;amp;disableRedirect=true&amp;amp;returnUrl=http%3A%2F%2Fwww.science.gu.se%2Faktuellt%2Fnyheter%2FNyheter%2BDetalj%2F%2Fkullerstenar-lurar-kroppens-immunforsvar.cid1050011" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7876</link><pubDate>Tue, 29 Nov 2011 17:39:37 PDT</pubDate></item><item><title>BWH researchers develop a vaccine prototype stronger than traditional vaccines</title><description>Brigham and Women's Hospital (BWH) researchers have created a vaccine  that is more potent than traditional vaccines available today. The  glycoconjugate vaccine prototype is 100 times more effective than  traditional glycoconjugate vaccines........&amp;gt; &lt;a href="http://www.brighamandwomens.org/about_bwh/publicaffairs/news/pressreleases/PressRelease.aspx?sub=0&amp;amp;PageID=1004" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7869</link><pubDate>Mon, 28 Nov 2011 17:15:05 PDT</pubDate></item><item><title>Bacteria responsible for common infections may protect themselves by stealing immune molecules</title><description>Bacteria responsible for middle ear infections, pink eye and sinusitis  protect  themselves from further immune attack by transporting molecules  meant to destroy them away from  their inner membrane target, according  to a study from Nationwide Children's Hospital.  The study, published  in the November issue of &lt;em&gt;PLoS Pathogens, &lt;/em&gt;is the first to describe a transporter system that bacteria use to ensure their survival.......&amp;gt; &lt;a href="http://www.physorg.com/news/2011-11-bacteria-responsible-common-infections-immune.html" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7847</link><pubDate>Thu, 17 Nov 2011 17:35:32 PDT</pubDate></item><item><title>Multiple malaria vaccine offers protection to people most at risk</title><description>A new malaria vaccine could be the first to tackle different forms of  the disease and help those most vulnerable to infection, a study  suggests.
The new vaccine is designed to trigger production of a range of  antibodies to fight the many different types of parasite causing the  disease.
Scientists created the vaccine by combining multiple versions of a  key protein found in many types of malaria parasite, which is known to  trigger production of antibodies upon infection.
Mixing multiple proteins from various parasite types induces  antibodies against a wide range of the parasites causing the disease.
Researchers from the University of Edinburgh, who developed the  vaccine, say that because malaria parasites exist in many forms, the  only way to gain natural immunity against all strains is by having  multiple bouts of the illness. A vaccine that overcomes this could be  especially useful in children and other vulnerable groups of people.
Many previous vaccines against malaria have had limited success  because they target only a limited part of the parasite population. The  new vaccine has also shown to be effective in animals.
Tests in blood samples from children in endemic areas showed that  the antibodies against this key protein offered improved protection  against the disease. Scientists now hope to carry out full-scale human  trials.
Malaria is spread by mosquito bites and affects people and animals,  mostly in sub-Saharan Africa. According to the World Health  Organisation, in 2009 the disease affected 225 million people and caused  an estimated 781,000 deaths, mostly among African children.
The study, published in &lt;em&gt;PLoS One&lt;/em&gt;, was supported by the European Commission.
Dr David Cavanagh, of the University of Edinburgh's School of  Biological Sciences, who led the study, said: "Our approach is novel  because it combines multiple antibody targets from different parasite  types, giving broader protection. This could prove to be a useful  vaccine."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7766</link><pubDate>Wed, 26 Oct 2011 17:30:51 PDT</pubDate></item><item><title>Researchers develop method to better estimate vaccine coverage</title><description>Immunizations are a valuable tool for controlling infectious diseases  among populations both in the U.S. and globally. Routine immunizations  and supplemental immunization activities, such as immunization  campaigns, are designed to provide immunization coverage to entire  populations. Current measurements used to determine the success and  rates of immunization can be flawed and inconsistent. According to a new  study led by researchers from the Johns Hopkins Bloomberg School of  Public Health, estimates of vaccination coverage can be significantly  improved by combining administrative data with survey data. The results  are featured in the October 2011 issue of &lt;em&gt;PLoS Medicine&lt;/em&gt;.
"Reliable estimates of vaccination coverage are key to managing  population immunization status," said Justin Lessler, lead author of the  study and an assistant professor with the Bloomberg School's Department  of Epidemiology. "Currently, the performance of routine and  supplemental immunization activities is measured by the administrative  method, which leads to coverage estimates that are often inconsistent  with the proportion reporting vaccination in cross-sectional surveys.  Furthermore,  administrative coverage does not tell you how many people  are systematically missed by vaccination activities. We estimated that  the size of the population never reached by any activity was high in  Sierra Leone and Madagascar, 31 percent and 21percent respectively. But  it was much lower in Ghana, only 7 percent. "
The widely used administrative method divides the number of doses  distributed by the size of the target population. Lessler, along with  colleagues from  Johns Hopkins, University of Oxford, Epicentre, and  Princeton University developed a method for estimating the effective  coverage of vaccination programs using cross-sectional surveys of  vaccine coverage combined with administrative data. The method was  applied using demographic health survey and administrative coverage data  reported to the WHO from measles vaccinations in Ghana, Madagascar and  Sierra Leone. They found estimates of routine supplemental immunization  activities coverage are substantially lower than administrative  estimates for Madagascar and Sierra Leone, and only slightly lower for  Ghana. In addition, their estimates of routine coverage are, in general,  lower than WHO and United Nations Children's Fund (UNICEF) estimates.
"This method not only attempts to correct coverage estimates, but  also distinguishes between issues of overall coverage and vaccine within  activity inefficiencies. For our technique to be useful, countries must  have cross-sectional data on vaccine coverage for children across a  range of ages, some of an age where they have been exposed to multiple  vaccination activities," said Derek Cummings.
"Estimates of the inefficiency of past vaccination activities and  the proportion not covered by any activity allow us to more accurately  predict the results of future activities and provide insight into the  ways in which vaccination programs are failing to meet their goals,"  adds Lessler.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7764</link><pubDate>Wed, 26 Oct 2011 17:28:25 PDT</pubDate></item><item><title>Study offers clues as to why some patients get infections from cardiac implants</title><description>New research suggests that some patients develop a potentially deadly  blood infection from their implanted cardiac devices because bacterial  cells in their bodies have gene mutations that allow them to stick to  the devices......&amp;gt; &lt;a href="http://www.nsf.gov/news/news_summ.jsp?cntn_id=122061&amp;amp;WT.mc_id=USNSF_51&amp;amp;WT.mc_ev=click" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7755</link><pubDate>Mon, 24 Oct 2011 16:55:01 PDT</pubDate></item><item><title>Antibody treatment protects monkeys from Hendra virus disease</title><description>A human antibody given to monkeys infected with the deadly Hendra  virus completely protected them from disease, according to a study  published by National Institutes of Health (NIH) scientists and their  collaborators. Hendra and the closely related Nipah virus, both rare  viruses that are part of the NIH biodefense research program, target the  lungs and brain and have human case fatality rates of 60 percent and  more than 75 percent, respectively. These diseases in monkeys mirror  what happens in humans, and the study results are cause for hope that  the antibody, named m102.4, ultimately may be developed into a possible  treatment for people who become infected with these viruses.
In May 2010, shortly after the NIH study in monkeys successfully  concluded, Australian health officials requested m102.4 for emergency  use in a woman and her 12-year-old daughter. They had been exposed to  Hendra virus from an ill horse that ultimately was euthanized. Both the  woman and child survived and showed no side effects from the treatment.
"This is an important research advance that illustrates how  scientific discoveries emerge through a steady stepwise process, and how  our investment in research on countermeasures for biodefense and  emerging infectious diseases can help global preparedness efforts," said  Anthony S. Fauci, M.D., director of the NIH's National Institute of  Allergy and Infectious Diseases (NIAID).
Hendra virus emerged in 1994 in Australia and primarily affects  horses, which can spread the disease to humans. No person-to-person  transmission of Hendra has been reported. Nipah virus emerged in 1998 in  Malaysia, and also has been found in Bangladesh and India. Nipah  appears to infect humans more easily than Hendra and can be transmitted  from person to person.
The NIAID-supported study, which appears online in Science  Translational Medicine, involved infecting 14 African green monkeys with  a lethal dose of Hendra virus. Twelve of the monkeys then received two  treatments with m102.4, one either at 10, 24, or 72 hours after being  infected, and another 48 hours later. All 12 monkeys treated with the  antibody survived. The two untreated control monkeys died eight days  after being infected.
The findings are the result of a series of studies carried out by  different research laboratories. A group from NIH's National Cancer  Institute and the Uniformed Services University of the Health Sciences  (USUHS) discovered m102.4 in 2006 and developed the antibody for use in  laboratory research. USUHS and Australian collaborators then developed  an animal study model of m102.4 in ferrets infected with Nipah virus;  the University of Texas Medical Branch and USUHS developed a monkey  study model of Hendra and Nipah infection; and together with  investigators from Boston University and NIAID's Rocky Mountain  Laboratories (RML) designed and carried out the antibody trial in  biosafety level-4 (BSL-4) laboratory space at RML. Because the Hendra  and Nipah viruses are so deadly and there is no licensed vaccine or  treatment for either of them, both viruses must be studied in  maximum-containment BSL-4 laboratories.
The World Health Organization reports 475 human cases of Nipah  through 2008, with 251 deaths. Through the same period, there have been  seven human Hendra cases with four fatalities. There also have been many  horse fatalities. In their study, the scientists cite a handful of  other outbreaks of Hendra virus in horses since 2008. Since June 2011,  there have been 18 outbreaks in Australia, primarily in Queensland and  New South Wales, with the latest reported Oct. 10.
Both viruses are spread by fruit bats, commonly known as flying  foxes, which are reservoirs for these viruses. The fruit bats, which are  resistant to the diseases, are found primarily in Australia but have  been found as far west as Africa, north to India and Pakistan, and east  to the Philippines.
Additional studies on m102.4 as a possible treatment and as a  preventive vaccine for Nipah and Hendra virus infections are being  planned.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7739</link><pubDate>Wed, 19 Oct 2011 17:10:58 PDT</pubDate></item><item><title>Penn researchers demonstrate efficacy of non-Hodgkin's lymphoma vaccine</title><description>An experimental vaccine developed by researchers at the University of Pennsylvania&amp;rsquo;s schools of Medicine and Veterinary Medicine is the first veterinary cancer vaccine of its kind that shows an  increase in survival time for dogs with spontaneous non-Hodgkin&amp;rsquo;s  lymphoma. The work shows for the first time the feasibility and  therapeutic efficacy of this alternative cell-based vaccine, which could  be employed in the treatment of a number of different cancer types......&amp;gt;&lt;a href="http://www.upenn.edu/pennnews/news/penn-researchers-demonstrate-efficacy-non-hodgkin-s-lymphoma-vaccine" target="_blank"&gt; Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7733</link><pubDate>Tue, 18 Oct 2011 16:36:21 PDT</pubDate></item><item><title>Scripps Research scientists reveal surprising picture of how powerful antibody neutralizes HIV</title><description>Researchers at The Scripps Research Institute have uncovered the  surprising details of how a powerful anti-HIV antibody grabs hold of the  virus. The findings, published in Science Express on October 13, 2011,  highlight a major vulnerability of HIV and suggest a new target for  vaccine development.
"What's unexpected and unique about this antibody is that it not  only attaches to the sugar coating of the virus but also reaches through  to grab part of the virus's envelope protein," said the report's  co-senior author Dennis Burton, a professor at The Scripps Research  Institute and scientific director of the International AIDS Vaccine  Initiative's (IAVI) Neutralizing Antibody Center, based on the Scripps  Research La Jolla campus.
"We can now start to think about constructing mimics of these viral  structures to use in candidate vaccines," said co-senior author Ian  Wilson, who is Hansen Professor of Structural Biology and member of the  Skaggs Institute for Chemical Biology at Scripps Research.
Other institutions in the United States, United Kingdom, Japan, and  the Netherlands contributed to the research as part of an ongoing global  HIV vaccine development effort.
&lt;strong&gt;
Getting a Better Grip on HIV
&lt;/strong&gt;
Researchers from the current team recently isolated the new antibody  and 16 others from the blood of HIV-infected volunteers, in work they  reported online in the journal Nature on August 17, 2011. Since the  1990s, Burton, Wilson, and other researchers have been searching for  such "broadly neutralizing" antibodies against HIV&amp;mdash;antibodies that work  against many of the various strains of the fast-mutating virus&amp;mdash;and by  now have found more than a dozen. PGT 128, the antibody described in the  new report, can neutralize about 70 percent of globally circulating HIV  strains by blocking their ability to infect cells. It also can do so  much more potently&amp;mdash;in other words, in smaller concentrations of antibody  molecules&amp;mdash;than any previously reported broadly neutralizing anti-HIV  antibody.
The new report illuminates why PGT 128 is so effective at  neutralizing HIV. Using the Wilson lab's expertise in X-ray  crystallography, Robert Pejchal, a research associate in the Wilson lab,  determined the structure of PGT 128 joined to its binding site on  molecular mockups of the virus, designed in part by Robyn Stanfield and  Pejchal in the Wilson group and Bill Schief, now an IAVI principal  scientist and associate professor at Scripps Research, and his group.  With these structural data, and by experimentally mutating and altering  the viral target site, they could see that PGT 128 works in part by  binding to glycans on the viral surface.
Thickets of these sugars normally surround HIV's envelope protein,  gp120, largely shielding it from attack by the immune system.  Nevertheless, PGT 128 manages to bind to two closely spaced glycans, and  at the same time reaches through the rest of the "glycan shield" to  take hold of a small part of structure on gp120 known as the V3 loop.  This penetration of the glycan shield by PGT 128 was also visualized by  electron microscopy with a trimeric form of the gp120/gp41 envelope  protein of HIV-1 by Reza Kayat and Andrew Ward of Scripps Research; this  revealed that the PGT 128 epitope appears to be readily accessible on  the virus.
"Both of these glycans appear in most HIV strains, which helps  explain why PGT 128 is so broadly neutralizing," said Katie J. Doores, a  research associate in the Burton lab who was one of the report's lead  authors. PGT 128 also engages V3 by its backbone structure, which  doesn't vary as much as other parts of the virus because it is required  for infection.
PGT 128's extreme potency is harder to explain. The antibody binds  to gp120 in a way that presumably disrupts its ability to lock onto  human cells and infect them. Yet it doesn't bind to gp120 many times  more tightly than other anti-HIV antibodies. The team's analysis hints  that PGT 128 may be extraordinarily potent because it also binds two  separate gp120 molecules, thus tying up not one but two cell-infecting  structures. Other mechanisms may also be at work.
&lt;strong&gt;
Toward an AIDS Vaccine
&lt;/strong&gt;
Researchers hope to use the knowledge of these antibodies' binding  sites on HIV to develop vaccines that stimulate a long-term&amp;mdash;perhaps  lifetime&amp;mdash;protective antibody response against those same vulnerable  sites.
"We'll probably need multiple targets on the virus for a successful  vaccine, but certainly PGT 128 shows us a very good target," said  Burton.
Intriguingly, the basic motif of PGT 128's target may mark a general  vulnerability for HIV. "Other research is also starting to suggest that  you can grab onto two glycans and a beta strand and get very potent and  broad neutralizing antibodies against HIV," Wilson said.</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7719</link><pubDate>Thu, 13 Oct 2011 16:59:32 PDT</pubDate></item><item><title>Cleveland Clinic study discovers new targets for treating inflammatory, autoimmune diseases</title><description>Researchers have discovered a cellular pathway that promotes  inflammation in diseases like asthma, rheumatoid arthritis, psoriasis,  inflammatory bowel disease, and multiple sclerosis. Understanding the  details of this pathway may provide opportunities for tailored  treatments of inflammatory and autoimmune diseases.
Discovery of this pathway was the work of an active collaboration  between Xiaoxia Li, Ph.D., and Thomas Hamilton, Ph.D., Department Chair,  both of the Department of Immunology at Lerner Research Institute of  Cleveland Clinic.
Their publications in &lt;em&gt;Nature Immunology&lt;/em&gt;, selected for a News  and Views article in the same issue, portray how a protein molecule  known as interleukin-17 (IL-17) spurs inflammation by recruiting  specific white blood cells to sites of infection and injury, producing a  strong, pathogenic response.
Being able to block this pathway may treat IL-17-induced  inflammatory diseases.  Molecular factors discovered by Li and Hamilton  make this concept a potential strategy.
"We are excited by the possibilities that this new research opens up  for developing improved therapeutics for these difficult diseases,"  Hamilton said.
"Being able to collaborate like this really expedites the science,"  Li added, "ultimately leading, we hope, to profound improvement for  those suffering from these autoimmune and inflammatory conditions."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7699</link><pubDate>Fri, 07 Oct 2011 17:36:28 PDT</pubDate></item><item><title>Immune mechanism blocks inflammation generated by oxidative stress</title><description>Conditions like atherosclerosis and age-related macular degeneration  (AMD) -- the most common cause of blindness among the elderly in western  societies -- are strongly linked to increased oxidative stress, the  process in which proteins, lipids and DNA damaged by oxygen free  radicals and related cellular waste accumulate, prompting an  inflammatory response from the body's innate immune system that results  in chronic disease.
In the October 6, 2011 issue of &lt;em&gt;Nature&lt;/em&gt;, researchers at the  University of California, San Diego School of Medicine, as part of an  international collaborative effort, identify a key protein that binds to  a molecule generated by oxidative stress, blocking any subsequent  inflammatory immune response. The scientists, led by senior author  Christoph J. Binder, assistant adjunct professor of medicine at UC San  Diego, principal investigator at the Center for Molecular Medicine of  the Austrian Academy of Sciences and professor at the Medical University  of Vienna, say their findings reveal important insights into how the  innate immune system responds to oxidative stress and might be exploited  to prevent and treat AMD and other chronic inflammatory diseases.
Specifically, Binder, Joseph L. Witztum, professor of medicine at UC  San Diego, and colleagues in Austria, Germany, England and Maryland  discovered that when lipids (fats) in cell membranes degrade through  oxidative stress, they produce a number of reactive products, including a  compound called malondialdehyde (MDA), which in turn modifies other  molecules to create novel oxidation-specific epitopes, the part of  antigens that draws the attention and inflammatory response of the  innate immune system.
The researchers noted, in particular, that MDA attracted an immune  system protein called complement factor H (CFH), which bound to it,  effectively blocking the uptake of MDA-modified proteins by macrophages,  a type of white blood cell charged with killing and eliminating foreign  invaders and substances. In in-vivo experiments, the researchers  reported that CFH neutralized the inflammatory effects of MDA in mice  retinas, limiting the inflammatory response associated with AMD and  other chronic diseases.
They also found that a specific mutation in the CFH protein, which  is associated with a four-to-seven-fold greater risk of developing AMD,  greatly diminished the ability of CFH to bind to MDA.
Binder said the findings further demonstrate the innate immune  system's important but not fully appreciated "house-keeping function,  defending against endogenous waste products and not just against foreign  microbial products."
Beyond that, he said the distinctive, protective role of CFH  represents a potential new therapeutic approach for treating AMD, heart  disease and other chronic conditions. "This activity of CFH can be used  for the development of neutralizing agents to mimic this function."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7689</link><pubDate>Wed, 05 Oct 2011 17:23:11 PDT</pubDate></item><item><title>Study: Impediment to some cancer immunotherapy involves the free radical peroxynitrite</title><description>Researchers at the Moffitt Cancer Center in Tampa, Fla., and colleagues have found that tumor cell resistance to  a specific cancer immunotherapy designed to kill cancer cells can be  blamed on a mechanism that involves the production of a free radical  peroxynitrite (PNT) that causes resistance to therapeutic cancer-killing  cells.......&amp;gt; &lt;a href="http://www.insidemoffitt.com/content.cfm?page_id=392&amp;amp;press_release_id=435" target="_blank"&gt;Full story&lt;/a&gt;</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7676</link><pubDate>Fri, 30 Sep 2011 18:28:36 PDT</pubDate></item><item><title>Modified vaccine shows promise in preventing malaria</title><description>Continuing a global effort to prevent malaria infections, Michigan  State University researchers have created a new malaria vaccine &amp;ndash; one  that combines the use of a disabled cold virus with an immune  system-stimulating gene &amp;ndash; that appears to increase the immune response  against the parasite that causes the deadly disease.
At the same time, the group led by Andrea Amalfitano of the College  of Osteopathic Medicine also discovered another immune-system  stimulating agent &amp;ndash; created at MSU and which has been successful in  improving immune responses in vaccines for diseases such as HIV &amp;ndash;  paradoxically made for a less effective malaria vaccine.
Both of the findings will help researchers develop more effective  vaccine platforms in general, and malaria vaccines specifically,  hopefully leading to human clinical trials soon, Amalfitano said. The  research is published in the current edition of &lt;em&gt;PLoS ONE.&lt;/em&gt;
"Researchers across the globe are working on ways to prevent people  from becoming infected with malaria," said Amalfitano of the disease  that kills up to a million people each year, mainly in sub-Saharan  Africa. "Some vaccines are showing promise, but they are not as  effective as they need to be for any mass distribution."
Amalfitano and his research team are focusing on one such vaccine  platform, spearheaded by the U.S. Army, that targets a certain gene on  the malaria parasite, a protein called Circumsporozoite Protein, or CSP.
That protein is thought to play a key role in creating an immune  response to the malaria parasite; past research shows people infected by  malaria multiple times will begin creating an immune response to this  protein, suggesting at some level it could be protective.
"What we are looking to do is improve the ability of the vaccine to  induce immune responses to that protein," Amalfitano said. "We are  adding genes to the vaccine to try and stimulate the immune system."
Those genetic agents, similar to chemical adjuvants, are stimulants  that improve the ability of vaccines to induce beneficial immune  responses in general.
In mouse models, the researchers used two such "gene-adjuvants": rEA  and EAT-2, both of which aimed to illicit improved immune responses to  the malaria CSP gene. Surprisingly, the rEA agent &amp;ndash; which was developed  at MSU in part by the late Barnett Rosenberg &amp;ndash; did not produce the  desired result and in fact seemed to worsen the animal's ability to  generate an immune response to CSP.
However, the EAT-2 gene-adjuvant stimulated the immune system in a  different way, and Amalfitano and his team were able to increase the  ability of the immune system to respond to CSP to a level that surpassed  currently available malaria vaccine systems.
"The results were surprising, but we were able to hit our goal  eventually," he said. "This research will help us as we create a viable  vaccine. While the way that rEA is trying to stimulate the immune system  may not be the best way for malaria, we did come up with an alternative  adjuvant to effectively target the parasite."
Amalfitano said the next step is to see if researchers can prevent  malaria in animal models using the EAT-2 gene-adjuvant: "Then we can  take the lessons learned and really go forward and do what's necessary  to feel confident to begin human trials."</description><link>http://www.labslink.com/ViewResearchNews.aspx?id=7655</link><pubDate>Mon, 26 Sep 2011 20:11:02 PDT</pubDate></item></channel></rss>