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人类口服伤寒减毒活疫苗株后的细胞毒性T淋巴细胞

Cytotoxic T lymphocytes after oral immunization with attenuated vaccine strains of Salmonella typhi in humans.

作者信息

Sztein M B, Tanner M K, Polotsky Y, Orenstein J M, Levine M M

机构信息

Department of Pediatrics, University of Maryland School of Medicine, Baltimore 21201, USA.

出版信息

J Immunol. 1995 Oct 15;155(8):3987-93.

PMID:7561107
Abstract

Not only viruses, but certain parasites and bacteria as well, can elicit CTL involved in mediating protection. It has been surmised that CTL able to lyse Salmonella typhi-infected cells are likely to be important in protecting against S. typhi, an intracellular bacterial infection, but heretofore this has not been demonstrated. Consequently, the presence of CTL activity against S. typhi-infected cells was investigated in human volunteers immunized with attenuated vaccine strains of S. typhi. Oral immunization with S. typhi strain CVD 908 elicited circulating CTL effector cells capable of killing S. typhi-infected autologous EBV-transformed cells. CTL activity was observed after 6 to 8 days of in vitro expansion in the presence of S. typhi-infected autologous EBV-transformed cells. Maximum CTL activity was observed 29 days after immunization. Depletion of CD8+ T cells eliminated or markedly reduced the CTL activity, while depletion of CD4+ T cells did not affect CTL responses. CTL activity was blocked by mAbs to human class I MHC Ags, but not by mAbs to class II MHC Ags. This first demonstration that oral immunization of volunteers with attenuated S. typhi elicits CD8+ T cell, MHC class I-restricted, CTL responses raises the possibility that CTL activity might play a significant role in protection during typhoid fever. It also encourages the future use of such attenuated strains as liver vector vaccines to stimulate specific CTL against relevant foreign Ags.

摘要

不仅病毒,某些寄生虫和细菌也能引发参与介导保护作用的细胞毒性T淋巴细胞(CTL)。据推测,能够裂解伤寒沙门氏菌感染细胞的CTL可能在抵御伤寒沙门氏菌(一种细胞内细菌感染)中发挥重要作用,但迄今为止尚未得到证实。因此,在接种伤寒沙门氏菌减毒疫苗株的人类志愿者中,研究了针对伤寒沙门氏菌感染细胞的CTL活性。口服伤寒沙门氏菌菌株CVD 908可引发循环CTL效应细胞,这些细胞能够杀死伤寒沙门氏菌感染的自体EB病毒转化细胞。在伤寒沙门氏菌感染的自体EB病毒转化细胞存在的情况下进行体外扩增6至8天后,观察到CTL活性。免疫后29天观察到最大CTL活性。CD8 + T细胞的耗竭消除或显著降低了CTL活性,而CD4 + T细胞的耗竭并未影响CTL反应。针对人类I类主要组织相容性复合体(MHC)抗原的单克隆抗体可阻断CTL活性,但针对II类MHC抗原的单克隆抗体则不能。首次证明用伤寒沙门氏菌减毒疫苗口服免疫志愿者可引发CD8 + T细胞、MHC I类限制性CTL反应,这增加了CTL活性可能在伤寒热期间的保护中发挥重要作用的可能性。这也鼓励未来使用这种减毒株作为肝脏载体疫苗来刺激针对相关外来抗原的特异性CTL。

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