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可溶性单核细胞衍生的 HLA II 类分子是否是免疫抑制活性的候选分子?

Are soluble monocyte-derived HLA class II molecules candidates for immunosuppressive activity?

作者信息

Claus R, Werner H, Schulze H A, Walzel H, Friemel H

机构信息

Institute of Immunology, Wilhelm Pieck University, Rostock, G.D.R.

出版信息

Immunol Lett. 1990 Dec;26(3):203-10. doi: 10.1016/0165-2478(90)90147-i.

Abstract

Supernatants of human blood monocyte cultures suppressed PHA responses (IL-2 synthesis, IL-2R expression, DNA synthesis) of autologous and allogeneic lymphocytes. The main suppressive activity was found in the 65-kDa (and 23-kDa) range. It could be incompletely neutralized by mAb specific for a non-polymorphic HLA DR determinant and could also be adsorbed to and eluted from an anti-DR immunoabsorbent column. On blots of monocyte lysates and monocyte culture supernatants, the mAb RoDR recognized antigens of nearly the same Mr. The hypothesis that soluble HLA DR alpha beta heterodimers or beta chains are likely candidates for the suppressor factor was confirmed by analogous effects of purified HLA DR molecules. We favor a model in which soluble MHC class II molecules (in contrast to surface-bound ones) may interfere with the association and cross-linking processes necessary for T cell activation by competing for CD4 binding sites.

摘要

人血单核细胞培养上清液可抑制自体和异体淋巴细胞的PHA反应(IL-2合成、IL-2R表达、DNA合成)。主要抑制活性存在于65 kDa(和23 kDa)范围内。它可被针对非多态性HLA DR决定簇的单克隆抗体不完全中和,也可吸附到抗DR免疫吸附柱上并从其上洗脱。在单核细胞裂解物和单核细胞培养上清液的印迹上,单克隆抗体RoDR识别分子量几乎相同的抗原。纯化的HLA DR分子的类似作用证实了可溶性HLA DRαβ异二聚体或β链可能是抑制因子的候选者这一假说。我们倾向于这样一种模型,即可溶性MHC II类分子(与表面结合的分子相反)可能通过竞争CD4结合位点来干扰T细胞激活所需的缔合和交联过程。

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