<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>Unitus DSpace</title>
  <link rel="alternate" href="http://http://dspace.unitus.it:80" />
  <subtitle>The DSpace digital repository system captures, stores, indexes, preserves, and distributes digital research material.</subtitle>
  <id>http://http://dspace.unitus.it:80</id>
  <updated>2013-05-24T05:15:09Z</updated>
  <dc:date>2013-05-24T05:15:09Z</dc:date>
  <entry>
    <title>Teleost intestinal immunology</title>
    <link rel="alternate" href="http://hdl.handle.net/2067/1559" />
    <author>
      <name>Rombout, Jan H.W.M.</name>
    </author>
    <author>
      <name>Abelli, Luigi</name>
    </author>
    <author>
      <name>Picchietti, Simona</name>
    </author>
    <author>
      <name>Scapigliati, Giuseppe</name>
    </author>
    <author>
      <name>Kiron, Viswanath</name>
    </author>
    <id>http://hdl.handle.net/2067/1559</id>
    <updated>2011-06-27T11:21:14Z</updated>
    <published>2009-12-31T23:00:00Z</published>
    <summary type="text">Title: Teleost intestinal immunology
Authors: Rombout, Jan H.W.M.; Abelli, Luigi; Picchietti, Simona; Scapigliati, Giuseppe; Kiron, Viswanath
Abstract: Teleosts clearly have a more diffuse gut associated lymphoid system, which is morphological and&#xD;
functional clearly different from the mammalian GALT. All immune cells necessary for a local immune&#xD;
response are abundantly present in the gut mucosa of the species studied and local immune responses&#xD;
can be monitored after intestinal immunization. Fish do not produce IgA, but a special mucosal IgM&#xD;
isotype seems to be secreted and may (partly) be the recently described IgZ/IgT. Fish produce a pIgR in&#xD;
their mucosal tissues but it is smaller (2 ILD) than the 4e5 ILD pIgR of higher vertebrates. Whether&#xD;
teleost pIgR is transcytosed and cleaved off in the same way needs further investigation, especially&#xD;
because a secretory component (SC) is only reported in one species. Teleosts also have high numbers of&#xD;
IEL, most of them are CD3-3&#xD;
þ/CD8-a&#xD;
þ and have cytotoxic and/or regulatory function. Possibly many of&#xD;
these cells are TCRgd cells and they may be involved in the oral tolerance induction observed in fish.&#xD;
Innate immune cells can be observed in the teleost gut from first feeding onwards, but B cells appear&#xD;
much later in mucosal compartments compared to systemic sites. Conspicuous is the very early presence&#xD;
of putative T cells or their precursors in the fish gut, which together with the rag-1 expression of&#xD;
intestinal lymphoid cells may be an indication for an extra-thymic development of certain T cells.&#xD;
Teleosts can develop enteritis in their antigen transporting second gut segment and epithelial cells, IEL&#xD;
and eosinophils/basophils seem to play a crucial role in this intestinal inflammation model. Teleost&#xD;
intestine can be exploited for oral vaccination strategies and probiotic immune stimulation. A variety of&#xD;
encapsulation methods, to protect vaccines against degradation in the foregut, are reported with&#xD;
promising results but in most cases they appear not to be cost effective yet. Microbiota in fish are clearly&#xD;
different from terrestrial animals. In the past decade a fast increasing number of papers is dedicated to&#xD;
the oral administration of a variety of probiotics that can have a strong health beneficial effect, but much&#xD;
more attention has to be paid to the immune mechanisms behind these effects. The recent development&#xD;
of gnotobiotic fish models may be very helpful to study the immune effects of microbiota and probiotics&#xD;
in teleosts.
Description: L'articolo è disponibile sul sito dell'editore http://www.sciencedirect.com/</summary>
    <dc:date>2009-12-31T23:00:00Z</dc:date>
  </entry>
</feed>

