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实验性病毒疫苗研究中人类CD4+和CD8+ T淋巴细胞反应的评估。

Assessment of human CD4+ and CD8+ T lymphocyte responses in experimental viral vaccine studies.

作者信息

Rothman A L, Yamada Y, Jameson J, Cruz J, West K, Green S, Ennis F A

机构信息

Center for Infectious Diseases and Vaccine Research, University of Massachusetts Medical Center, Worcester 01655, USA.

出版信息

Dev Biol Stand. 1998;95:95-104.

PMID:9855419
Abstract

The traditional in vitro correlate of immunological protection is the induction by a vaccine of neutralizing antibodies against the virus. It was formerly assumed that protection induced by a vaccine was solely due to neutralizing antibodies. Neutralizing antibodies are potent in the prevention of certain diseases, but virus-specific CD4+ T helper cells aid in the proliferation of specific antigen-triggered B cells to make antibodies. CD8+ T cells are responsible for eliminating virus-infected cells during viral illness, and may act as a second line of defence by becoming activated and eliminating any cells that become infected despite the presence of neutralizing antibodies, for example because of a large challenge dose or antigenic variation at the antibody combining sites. We will briefly review our approaches for measuring human virus-specific CD4+ and CD8+ T cell responses to experimental vaccines. It is critically important to have sensitive, quality controlled assays, including positive controls. There are many potential variables in human T cell assays and pitfalls, which usually result in negative CTL results. Uninterpretable data are to be expected unless adequate preliminary testing has been done to establish sensitive, specific and controlled human antigen specific CD4+ and CD8+ T cell assays.

摘要

免疫保护的传统体外相关指标是疫苗诱导产生针对病毒的中和抗体。以前人们认为疫苗诱导的保护完全归因于中和抗体。中和抗体在预防某些疾病方面很有效,但病毒特异性CD4 + T辅助细胞有助于特定抗原触发的B细胞增殖以产生抗体。CD8 + T细胞负责在病毒感染期间清除被病毒感染的细胞,并且可能通过被激活并清除任何尽管存在中和抗体但仍被感染的细胞而作为第二道防线,例如由于大量的攻击剂量或抗体结合位点处的抗原变异。我们将简要回顾我们用于测量人类病毒特异性CD4 +和CD8 + T细胞对实验性疫苗反应的方法。拥有灵敏、质量可控的检测方法(包括阳性对照)至关重要。人类T细胞检测存在许多潜在变量和陷阱,这通常会导致细胞毒性T淋巴细胞(CTL)检测结果为阴性。除非已经进行了充分的初步检测以建立灵敏、特异且可控的人类抗原特异性CD4 +和CD8 + T细胞检测方法,否则无法解释的数据是可以预料的。

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