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免疫佐剂通过诱导Bcl-3来促进活化T细胞的存活。

Immunological adjuvants promote activated T cell survival via induction of Bcl-3.

作者信息

Mitchell T C, Hildeman D, Kedl R M, Teague T K, Schaefer B C, White J, Zhu Y, Kappler J, Marrack P

机构信息

Howard Hughes Medical Institute, University of Colorado Health Sciences Center, Denver, CO 80206, USA.

出版信息

Nat Immunol. 2001 May;2(5):397-402. doi: 10.1038/87692.

Abstract

Injection of soluble protein antigen into animals causes abortive proliferation of the responding T cells. Immunological adjuvants boost T cell responses at least in part by increasing the survival of activated T cells during and after the initial proliferative phase of their clonal expansion. To understand how adjuvants promote T cell survival, we used gene microarrays to analyze gene expression in T cells activated either with antigen alone or in the presence of two different adjuvants. Among the genes whose expression was increased by both adjuvants was the IkappaB family member Bcl-3. Retroviral infection experiments showed that expression of Bcl-3 increased survival of activated T cells in vitro and in vivo. Adjuvants may therefore improve survival of activated T cells via induction of Bcl-3.

摘要

向动物体内注射可溶性蛋白抗体会导致应答性T细胞的增殖失败。免疫佐剂至少部分地通过在激活的T细胞克隆扩增的初始增殖阶段及之后增加其存活率来增强T细胞反应。为了了解佐剂如何促进T细胞存活,我们使用基因微阵列分析单独用抗原或在两种不同佐剂存在的情况下激活的T细胞中的基因表达。两种佐剂均使表达增加的基因中有IκB家族成员Bcl-3。逆转录病毒感染实验表明,Bcl-3的表达在体外和体内均增加了激活的T细胞的存活率。因此,佐剂可能通过诱导Bcl-3来提高激活的T细胞的存活率。

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