<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Allergy, Asthma and Immunology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>18</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Th22 Cells Contribution in Immunopathogenesis of Rheumatic Diseases</title>
    <FirstPage>246</FirstPage>
    <LastPage>254</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Azizi</LastName>
        <affiliation locale="en_US">Imam Hassan Mojtaba Hospital, Alborz University of Medical Sciences, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Anita</FirstName>
        <LastName>Simhag</LastName>
        <affiliation locale="en_US">Karolinska Institutet Science Park AB, Huddinge, Sweden</affiliation>
      </Author>
      <Author>
        <FirstName>Nadia</FirstName>
        <LastName>M-M-El Rouby</LastName>
        <affiliation locale="en_US">Department of Histology, Dubai Medical College, Dubai, UAE</affiliation>
      </Author>
      <Author>
        <FirstName>Abbas</FirstName>
        <LastName>Mirshafiey</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>18</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Newly&#xA0; identified&#xA0; T&#xA0; helper&#xA0; cell&#xA0; 22&#xA0; (Th22)&#xA0; is&#xA0; a&#xA0; subset&#xA0; of&#xA0; CD4+T&#xA0; cells&#xA0; with&#xA0; specific properties apart from other known CD4+ T cell subsets with distinguished gene expression and function. Th22 cells are characterized by production of a distinct profile of effector cytokines, including interleukin (IL)-22, IL-13, and tumor necrosis factor-&#x3B1; (TNF-&#x3B1;). The levels of Th22 and related cytokine IL-22 are increased in various autoimmune diseases and positively associated with some rheumatic diseases such as rheumatoid arthritis, systemic lupus erythematosus, behcet's disease, ankylosing spondylitis and psoriatic arthritis. In summary, IL-22 and Th22 cells play a significant and complicated role in inflammatory and autoimmune&#xA0; rheumatic&#xA0; diseases,&#xA0; therefore,&#xA0; targeting&#xA0; IL-22&#xA0; or&#xA0; Th22&#xA0; have&#xA0; unique&#xA0; and attractive advantages due to the fact that Th22 subset is recently identified and its associated research is extremely limited. This review discusses the role of Th22 and its cytokine IL-22 in the immunopathogenesis of rheumatic disease.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/564</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/564/449</pdf_url>
  </Article>
</Articles>
