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<art>
   <ui>ar2234</ui>
   <ji>ARJ</ji>
   <fm>
      <dochead>Poster presentation</dochead>
      <bibl>
         <title>
            <p>IL-21 and BAFF/BLyS synergize in stimulating plasma cell differentiation from human marginal zone B cells as well as from circulating peripheral blood B cells from autoimmune patients</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Ettinger</snm>
               <fnm>Rachel</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Kuchen</snm>
               <fnm>Stefan</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Sims</snm>
               <mi>P</mi>
               <fnm>Gary</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>Robbins</snm>
               <fnm>Rachel</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A5">
               <snm>Withers</snm>
               <fnm>David</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A6">
               <snm>Fischer</snm>
               <mi>T</mi>
               <fnm>Randy</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A7">
               <snm>Lipsky</snm>
               <mi>E</mi>
               <fnm>Peter</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Autoimmunity Branch, NIAMS, National Institutes of Health, Bethesda, MD, USA</p>
            </ins>
         </insg>
         <source>Arthritis Research &amp; Therapy</source>
         <supplement>
            <title>
               <p>6<sup>th </sup>Global Arthritis Research Network (GARN) Meeting</p>
            </title>
            <editor>Steffen Gay and Peter E Lipsky</editor>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>6<sup>th </sup>Global Arthritis Research Network (GARN) Meeting</p>
            </title>
            <location>Zurich, Switzerland</location>
            <date-range>10&#8211;13 May 2007</date-range>
            <url>http://www.ciaomed.org/garn.cfm</url>
         </conference>
         <issn>1478-6354</issn>
         <pubdate>2007</pubdate>
         <volume>9</volume>
         <issue>Suppl 3</issue>
         <fpage>P8</fpage>
         <url>http://arthritis-research.com/content/9/S3/P8</url>
         <xrefbib>
            <pubid idtype="doi">10.1186/ar2234</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>19</day>
               <month>10</month>
               <year>2007</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2007</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
   </fm>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>IL-21 promotes plasma cell (PC) differentiation while BAFF promotes B-cell survival. Here, we report that IL-21 synergizes with BAFF to elicit BLIMP-1 induction, PC differentiation and IgG production from a novel population of human splenic memory B cells. These human marginal zone analogue B cells are exquisitely sensitive to IL-21 and BAFF in the absence of further co-stimulation. The ability of IgG<sup>+ </sup>marginal zone analogue to respond specifically and exclusively to IL-21 and BAFF demonstrates that they are uniquely poised to respond to antigen-independent signals and differentiate into IgG-producing PC, thereby replenishing serologic memory. Importantly, peripheral blood B cells from a portion of patients with systemic lupus erythematosus and rheumatoid arthritis were highly responsive to stimulation with IL-21 and BAFF. These data suggest that IL-21 and BAFF may be capable of inducing PC differentiation from memory B cells with autoreactive specificities and thereby contribute to autoimmunity.</p>
      </sec>
   </bdy>
</art>
