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用1型呼肠孤病毒/L进行肠道黏膜免疫可刺激派伊尔结中的病毒特异性细胞毒性T细胞前体以及IgA记忆细胞。

Gut mucosal immunization with reovirus serotype 1/L stimulates virus-specific cytotoxic T cell precursors as well as IgA memory cells in Peyer's patches.

作者信息

London S D, Rubin D H, Cebra J J

出版信息

J Exp Med. 1987 Mar 1;165(3):830-47. doi: 10.1084/jem.165.3.830.

Abstract

In this report we have shown that reovirus 1/L is an effective mucosal immunogen capable of generating a cytotoxic T cell (CTL) and associated helper T cell response to the nominal antigens associated with reovirus 1/L. The effectors that mediate reovirus-specific cytotoxicity are Thy-1+, Lyt-2+, and major histocompatibility complex (MHC)-restricted in their recognition of reovirus antigens, and can therefore be classified as CTLs. Frequency analysis of precursor CTLs occurring in Peyer's patches (PP) and peripheral lymph nodes (PLN) 6 d and 6 mo after intraduodenal stimulation have demonstrated that a persistent gradient of precursors is established, with higher frequencies present in PP. The generation of a CTL response in PP may be important in preferentially repopulating mucosal tissues with effector CTLs that could result in the local containment of infections in the gut. We also found that reovirus 1/L generates a virus-specific B cell response that is dominated by IgA memory cells after intraduodenal immunization. We hypothesize that the efficacy of reovirus 1/L at stimulating T and B cells in the gut mucosa is related to its ability to selectively enter PP via microfold (M) cells after enteric application. In this study we have also demonstrated that PP cells, upon in vitro culture and unrelated to prior reovirus priming, can generate natural killer-like (NK) cytotoxic activity. This may be an in vitro correlate of the in vivo generation of effectors that may populate mucosal tissues (i.e., the intestinal epithelium) with NK-like effector cells.

摘要

在本报告中,我们已表明呼肠孤病毒1/L是一种有效的粘膜免疫原,能够产生细胞毒性T细胞(CTL)以及针对与呼肠孤病毒1/L相关的名义抗原的相关辅助性T细胞应答。介导呼肠孤病毒特异性细胞毒性的效应细胞为Thy-1⁺、Lyt-2⁺,且在识别呼肠孤病毒抗原时受主要组织相容性复合体(MHC)限制,因此可归类为CTL。对十二指肠内刺激后6天和6个月在派尔集合淋巴结(PP)和外周淋巴结(PLN)中出现的前体CTL进行频率分析表明,建立了持续的前体梯度,PP中的频率更高。PP中CTL应答的产生可能在优先用效应CTL重新填充粘膜组织方面很重要,这可能导致肠道感染的局部控制。我们还发现,呼肠孤病毒1/L在十二指肠内免疫后产生以IgA记忆细胞为主的病毒特异性B细胞应答。我们推测呼肠孤病毒1/L在肠道粘膜中刺激T和B细胞的功效与其在肠道应用后通过微褶(M)细胞选择性进入PP的能力有关。在本研究中,我们还证明,PP细胞在体外培养时,与先前的呼肠孤病毒引发无关,可产生自然杀伤样(NK)细胞毒性活性。这可能是体内产生效应细胞的体外相关因素,这些效应细胞可能会使粘膜组织(即肠上皮)充满NK样效应细胞。

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本文引用的文献

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