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人T细胞克隆分泌不同于γ干扰素的巨噬细胞激活因子。

Secretion of a macrophage-activating factor distinct from interferon-gamma by human T cell clones.

作者信息

Andrew P W, Rees A D, Scoging A, Dobson N, Matthews R, Whittall J T, Coates A R, Lowrie D B

出版信息

Eur J Immunol. 1984 Oct;14(10):962-4. doi: 10.1002/eji.1830141018.

Abstract

Supernatants from clones of human T lymphocytes that were responding to a purified Mycobacterium tuberculosis antigen were able to activate macrophages and macrophage-like myeloma cells (U937) to release increased amounts of the microbicidal agent hydrogen peroxide. The activity was not neutralized by monoclonal antibody against interferon-gamma (IFN-gamma), was greater than could be accounted for by the IFN-gamma activity in the supernatants, and was separated from IFN-gamma by high performance liquid chromatography. It is evident that IFN-gamma is not the only macrophage activator released by T lymphocytes responding to microbial antigen, and may not even be the main one to enhance antimicrobial activity in infections such as tuberculosis.

摘要

对纯化的结核分枝杆菌抗原产生反应的人T淋巴细胞克隆的上清液,能够激活巨噬细胞和巨噬细胞样骨髓瘤细胞(U937),使其释放出更多的杀微生物剂过氧化氢。该活性不能被抗γ干扰素(IFN-γ)单克隆抗体中和,其活性大于上清液中IFN-γ活性所能解释的程度,并且通过高效液相色谱法与IFN-γ分离。显然,IFN-γ不是对微生物抗原产生反应的T淋巴细胞释放的唯一巨噬细胞激活剂,甚至可能不是增强结核病等感染中抗菌活性的主要激活剂。

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