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在缺乏功能性Th1或Th2细胞的情况下,口服诱导的外周无反应性得以维持。

Orally induced peripheral nonresponsiveness is maintained in the absence of functional Th1 or Th2 cells.

作者信息

Shi H N, Grusby M J, Nagler-Anderson C

机构信息

Mucosal Immunology Laboratory, Massachusetts General Hospital, Charlestown 02129, USA.

出版信息

J Immunol. 1999 May 1;162(9):5143-8.

Abstract

Intragastric administration of soluble protein Ags results in peripheral tolerance to the fed Ag. To examine the role of cytokine regulation in the induction of oral tolerance, we fed OVA to mice deficient in Th1 (Stat 4-/-) and Th2 (Stat 6-/-) cells and compared their response to that of normal BALB/c controls. We found that, in spite of these deficiencies, OVA-specific peripheral cell-mediated and humoral nonresponsiveness was maintained in both Stat 4-/- and Stat 6-/- mice. In the mucosa, both Peyer's patch T cell proliferative responses and OVA-specific fecal IgA were reduced in Stat 4-/- and Stat 6-/- mice fed OVA but not in normal BALB/c controls. Mucosal, but not peripheral, nonresponsiveness was abrogated by the inclusion of a neutralizing Ab to TGF-beta in the culture medium. Our results show that, in the periphery, tolerance to oral Ag can be induced in both a Th1- or Th2-deficient environment. In the mucosa, however, the absence of Th1 and Th2 cytokines can markedly affect this response, perhaps by regulation of TGF-beta-secreting cells.

摘要

胃内给予可溶性蛋白抗原可导致对所摄入抗原的外周耐受。为了研究细胞因子调节在口服耐受诱导中的作用,我们给缺乏Th1(Stat 4-/-)和Th2(Stat 6-/-)细胞的小鼠喂食卵清蛋白(OVA),并将它们的反应与正常BALB/c对照小鼠的反应进行比较。我们发现,尽管存在这些缺陷,Stat 4-/-和Stat 6-/-小鼠中OVA特异性外周细胞介导的和体液无反应性仍得以维持。在黏膜中,喂食OVA的Stat 4-/-和Stat 6-/-小鼠的派尔集合淋巴结T细胞增殖反应和OVA特异性粪便IgA均降低,但正常BALB/c对照小鼠则不然。在培养基中加入抗转化生长因子-β(TGF-β)的中和抗体可消除黏膜而非外周的无反应性。我们的结果表明,在外周,在缺乏Th1或Th2的环境中均可诱导对口服抗原的耐受。然而,在黏膜中,Th1和Th2细胞因子的缺失可能通过调节分泌TGF-β的细胞而显著影响这种反应。

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