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针对病毒感染的同基因细胞的细胞毒性T细胞的体外初次诱导。

In vitro primary induction of cytotoxic T cells against virus-infected syngeneic cells.

作者信息

Blanden R V, Kees U, Dunlop M B

出版信息

J Immunol Methods. 1977;16(1):73-89. doi: 10.1016/0022-1759(77)90040-0.

Abstract

An in vitro method is described for primary induction of murine cytotoxic T cells against syngeneic cells infected with ectromelia or lymphocytic choriomeningitis (LCM) virus. Cytotoxicity was assayed by 51Cr release from macrophage or L929 target cells. Cytotoxic activity was sensitive to anti-theta and complement and was expressed only against target cells infected with the same virus and sharing H-2K or H-2D genes with the infected stimulator cells. The crucial factors in generating responses were mouse strain, responder: stimulator ratio, nature of infected stimulator cells, and presence of sufficient macrophages. C57BL/6 cells were less demanding than CBA/H and BALB/c cells. Under optimal conditions defined here, the in vitro response had similar kinetics and potency to the primary response in the spleen in vivo.

摘要

本文描述了一种体外方法,用于初次诱导小鼠细胞毒性T细胞,使其针对感染痘苗病毒或淋巴细胞性脉络丛脑膜炎(LCM)病毒的同基因细胞产生反应。通过巨噬细胞或L929靶细胞释放51Cr来检测细胞毒性。细胞毒性活性对抗θ抗体和补体敏感,并且仅针对感染相同病毒且与感染的刺激细胞共享H-2K或H-2D基因的靶细胞表现出来。产生反应的关键因素包括小鼠品系、反应细胞与刺激细胞的比例、感染的刺激细胞的性质以及足够巨噬细胞的存在。C57BL/6细胞比CBA/H和BALB/c细胞要求更低。在此定义的最佳条件下,体外反应在动力学和效力方面与体内脾脏中的初次反应相似。

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