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卡介苗细胞壁骨架诱导人树突状细胞成熟:Toll样受体的作用

Maturation of human dendritic cells by cell wall skeleton of Mycobacterium bovis bacillus Calmette-Guérin: involvement of toll-like receptors.

作者信息

Tsuji S, Matsumoto M, Takeuchi O, Akira S, Azuma I, Hayashi A, Toyoshima K, Seya T

机构信息

Department of Immunology, Osaka Medical Center for Cancer and Cardiovascular Diseases, Higashinari-ku, Osaka 537-8511, Japan.

出版信息

Infect Immun. 2000 Dec;68(12):6883-90. doi: 10.1128/IAI.68.12.6883-6890.2000.

Abstract

The constituents of mycobacteria are an effective immune adjuvant, as observed with complete Freund's adjuvant. In this study, we demonstrated that the cell wall skeleton of Mycobacterium bovis bacillus Calmette-Guérin (BCG-CWS), a purified noninfectious material consisting of peptidoglycan, arabinogalactan, and mycolic acids, induces maturation of human dendritic cells (DC). Surface expression of CD40, CD80, CD83, and CD86 was increased by BCG-CWS on human immature DC, and the effect was similar to those of interleukin-1beta (IL-1beta), tumor necrosis factor alpha (TNF-alpha), heat-killed BCG, and viable BCG. BCG-CWS induced the secretion of TNF-alpha, IL-6, and IL-12 p40. CD83 expression was increased by a soluble factor secreted from BCG-CWS-treated DC and was completely inhibited by monoclonal antibodies against TNF-alpha. BCG-CWS-treated DC stimulated extensive allogeneic mixed lymphocyte reactions. The level of TNF-alpha secreted through BCG-CWS was partially suppressed in murine macrophages with no Toll-like receptor 2 (TLR 2) or TLR4 and was completely lost in TLR2 and TLR4 double-deficient macrophages. These results suggest that the BCG-CWS induces TNF-alpha secretion from DC via TLR2 and TLR4 and that the secreted TNF-alpha induces the maturation of DC per se.

摘要

正如在完全弗氏佐剂中所观察到的那样,分枝杆菌的成分是一种有效的免疫佐剂。在本研究中,我们证明了卡介苗(BCG)的细胞壁骨架(BCG-CWS),一种由肽聚糖、阿拉伯半乳聚糖和分枝菌酸组成的纯化的无感染性物质,可诱导人树突状细胞(DC)成熟。BCG-CWS可增加人未成熟DC表面CD40、CD80、CD83和CD86的表达,其效果与白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、热灭活卡介苗和活卡介苗相似。BCG-CWS可诱导TNF-α、IL-6和IL-12 p40的分泌。BCG-CWS处理的DC分泌的一种可溶性因子可增加CD83的表达,且该作用可被抗TNF-α单克隆抗体完全抑制。BCG-CWS处理的DC可刺激广泛的同种异体混合淋巴细胞反应。在无Toll样受体2(TLR 2)或TLR4的小鼠巨噬细胞中,通过BCG-CWS分泌的TNF-α水平部分受到抑制,而在TLR-2和TLR4双缺陷巨噬细胞中则完全丧失。这些结果表明,BCG-CWS通过TLR2和TLR4诱导DC分泌TNF-α,且分泌的TNF-α本身可诱导DC成熟。

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