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人类针对病毒感染靶细胞的细胞介导细胞毒性。II. 干扰素诱导与自然杀伤细胞的激活。

Cell-mediated cytotoxicity against virus-infected target cells in humans. II. Interferon induction and activation of natural killer cells.

作者信息

Santoli D, Trinchieri G, Koprowski H

出版信息

J Immunol. 1978 Aug;121(2):532-8.

PMID:150448
Abstract

The mechanisms by which human lymphocytes lyse virus-infected allogeneic fibroblast cultures were analyzed with particular consideration of the role of anti-viral antibodies and interferon. Human cells infected with viruses were able to induce high levels of interferon upon contact with human lymphocytes. Interferon, whether produced by lymphocytes after direct infection with virus or induced upon exposure of lymphocytes to virus-infected fibroblasts, appeared to be responsible for enhancing the cytotoxic efficiency of the natural killer cell against the infected target. Activation of cytotoxic lymphocytes occurred as early as 6 hr after addition of interferon and increased up to 24 hr. Antibody-dependent cell-mediated cytotoxicity (Ab-CMC) could be easily induced by sensitization of infected target cells with antiviral antibodies and could be detected at 4 hr from the beginning of the cytotoxic test, before the effect of interferon on the natural killer cell was evident. However, the antibody-dependent effector cell was inactive after 4 hr of incubation. F(ab')2 fragments of rabbit anti-human IgG completely inhibited Ab-CMC but did not at all affect the spontaneous cytotoxic activity of the effector cells against virus-infected target.

摘要

分析了人类淋巴细胞裂解病毒感染的同种异体成纤维细胞培养物的机制,特别考虑了抗病毒抗体和干扰素的作用。感染病毒的人类细胞与人类淋巴细胞接触后能够诱导产生高水平的干扰素。干扰素,无论是淋巴细胞直接感染病毒后产生的,还是淋巴细胞暴露于病毒感染的成纤维细胞后诱导产生的,似乎都负责增强自然杀伤细胞对感染靶标的细胞毒性效率。细胞毒性淋巴细胞的激活早在加入干扰素后6小时就出现,并持续增加至24小时。通过用抗病毒抗体致敏感染的靶细胞,可以很容易地诱导抗体依赖性细胞介导的细胞毒性(Ab-CMC),并且在细胞毒性试验开始后4小时就能检测到,此时干扰素对自然杀伤细胞的作用尚不明显。然而,抗体依赖性效应细胞在孵育4小时后就失去活性。兔抗人IgG的F(ab')2片段完全抑制Ab-CMC,但对效应细胞对病毒感染靶标的自发细胞毒性活性完全没有影响。

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