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CD40配体缺陷小鼠中T细胞介导的巨噬细胞活化受损。

Impaired T cell-mediated macrophage activation in CD40 ligand-deficient mice.

作者信息

Stout R D, Suttles J, Xu J, Grewal I S, Flavell R A

机构信息

Department of Microbiology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City 37614-0579, USA.

出版信息

J Immunol. 1996 Jan 1;156(1):8-11.

PMID:8598498
Abstract

The expression of the ligand for CD40 (CD40L) is critical for induction of T cell-dependent Ab responses. To examine how critical the expression of CD40L is for induction of cell-mediated immune responses, the ability of T cells from CD40L knockout mice to activate macrophage effector function was assessed. CD4+ T cells from CD40L-knockout mice were fourfold less effective than +/+ T cells in activating the nitric oxide response in allogeneic macrophages. CD40L-knockout T cells that were fixed with paraformaldehyde after a 6-h activation period, a time point at which CD40L dominates the macrophage-activating capability of the T cell, could activate neither macrophage production of inflammatory cytokines (TNF-alpha) nor generation of reactive nitrogen intermediates. After 24 h of activation, however, both CD40L-knockout and +/+ T cells could induce similar but weak responses from the macrophages. This study demonstrates that animals deficient in CD40L expression display a deficiency in T cell-dependent macrophage-mediated immune responses.

摘要

CD40配体(CD40L)的表达对于诱导T细胞依赖性抗体反应至关重要。为了研究CD40L的表达对于诱导细胞介导的免疫反应有多关键,评估了来自CD40L基因敲除小鼠的T细胞激活巨噬细胞效应功能的能力。在激活同种异体巨噬细胞的一氧化氮反应方面,来自CD40L基因敲除小鼠的CD4⁺T细胞的效力比野生型T细胞低四倍。在激活6小时后(此时CD40L在T细胞的巨噬细胞激活能力中占主导地位)用多聚甲醛固定的CD40L基因敲除T细胞,既不能激活巨噬细胞产生炎性细胞因子(TNF-α),也不能激活活性氮中间体的生成。然而,激活24小时后,CD40L基因敲除T细胞和野生型T细胞都能诱导巨噬细胞产生相似但较弱的反应。这项研究表明,缺乏CD40L表达的动物在T细胞依赖性巨噬细胞介导的免疫反应中存在缺陷。

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