巨噬细胞在生发中心反应中的调控作用。

J P Smith, G F Burton, J G Tew, A K Szakal
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引用次数: 64

摘要

可感触体巨噬细胞(TBM)长期以来被认为只是凋亡淋巴细胞的清道夫,它位于生发中心独特的微环境中,靠近保留抗原的滤泡树突状细胞(FDC)。观察到TBM内吞FDC-iccosomal(免疫复合物包被体)抗原提示TBM可能呈递该抗原并帮助调节生发中心反应。为了检测抗原呈递,使用卵清蛋白(OVA)特异性T(H)杂交瘤3DO-54.8,在接受有效的OVA呈递时产生IL-2,作为对携带OVA的TBM的应答者。结果表明,含ova的TBM不能诱导IL-2的产生。此外,将TBM添加到IL-2诱导阳性对照(B细胞)中不仅不能增加IL-2的产生,而且TBM显著(55-90%)降低了B细胞对IL-2的诱导。与其他非生殖中心淋巴结巨噬细胞相比,我们发现TBM富含前列腺素,在培养物中加入吲哚美辛可以逆转TBM的抑制作用。在加入阳性对照培养物之前,从富集制剂中去除TBM也消除了对IL-2产生的抑制作用。这些数据支持这样一个概念,即在生发中心独特的微环境中,TBM可能专门下调生发中心的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tingible body macrophages in regulation of germinal center reactions.

Tingible body macrophages (TBM), long thought simply as scavengers of apoptotic lymphocytes, are located in the unique microenvironment of germinal centers in close proximity to antigen-retaining follicular dendritic cells (FDC). Observations that TBM endocytose FDC-iccosomal (immune-complex coated bodies) antigen suggested that TBM might present this antigen and help regulate the germinal center reaction. To test for antigen presentation, the ovalbumin (OVA)-specific T(H) hybridoma, 3DO-54.8, which produces IL-2 on receiving effective presentation of OVA, were used as responders to OVA-bearing TBM. Results showed that OVA-bearing TBM failed to induce IL-2 production. Furthermore, addition of TBM to IL-2-inducing positive controls (B cells) not only failed to augment IL-2 production, but rather TBM significantly (55-90%) reduced B-cell induction of IL-2. We found that TBM were rich in prostaglandin by comparison with other nongerminal center lymph node macrophages and that addition of indomethacin to the cultures reversed the inhibitory effect of TBM. Depletion of TBM from enriched preparations, prior to addition to positive control cultures, also abrogated the inhibitory effect on IL-2 production. These data support the concept that TBM, within the unique microenvironment of germinal centers, may be specialized to downregulate the germinal center reaction.

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