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白细胞介素-4和粒细胞巨噬细胞集落刺激因子可选择性增加人单核细胞上的HLA-DR和HLA-DP抗原,但不增加HLA-DQ抗原。

IL-4 and granulocyte-macrophage colony-stimulating factor selectively increase HLA-DR and HLA-DP antigens but not HLA-DQ antigens on human monocytes.

作者信息

Gerrard T L, Dyer D R, Mostowski H S

机构信息

Division of Cytokine Biology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892.

出版信息

J Immunol. 1990 Jun 15;144(12):4670-4.

PMID:2112573
Abstract

A number of cytokines were tested for their ability to modulate HLA-DR Ag expression on normal human monocytes. IL-4, granulocyte-macrophage (GM)-CSF as well as IFN-gamma were able to increase HLA-DR Ag expression on monocytes. IFN-alpha was also able to augment HLA-DR Ag expression, but to a lesser degree. Macrophage-CSF, granulocyte-CSF, TNF-alpha, TNF-beta, and IL-6 were not able to augment HLA-DR Ag expression. There were distinct patterns in the ability of different cytokines to augment class II histocompatibility Ag expression. IL-4 and GM-CSF selectively increased only HLA-DR and HLA-DP, but did not increase HLA-DQ antigens on monocytes. IFN-gamma, however, was able to augment the expression of HLA-DR, HLA-DP, and HLA-DQ Ag. Combinations of IFN-gamma with either IL-4 or GM-CSF did not show any synergy for the augmentation of any of the class II antigens on monocytes.

摘要

检测了多种细胞因子调节正常人单核细胞上HLA - DR抗原表达的能力。白细胞介素 - 4(IL - 4)、粒细胞 - 巨噬细胞(GM)集落刺激因子以及γ干扰素(IFN - γ)能够增加单核细胞上HLA - DR抗原的表达。α干扰素(IFN - α)也能够增强HLA - DR抗原的表达,但程度较小。巨噬细胞集落刺激因子、粒细胞集落刺激因子、肿瘤坏死因子 - α(TNF - α)、肿瘤坏死因子 - β(TNF - β)和白细胞介素 - 6不能增强HLA - DR抗原的表达。不同细胞因子增强Ⅱ类组织相容性抗原表达的能力存在明显差异。IL - 4和GM - CSF仅选择性增加单核细胞上的HLA - DR和HLA - DP,但不增加HLA - DQ抗原。然而,IFN - γ能够增强HLA - DR、HLA - DP和HLA - DQ抗原的表达。IFN - γ与IL - 4或GM - CSF的组合在增强单核细胞上任何Ⅱ类抗原表达方面均未显示出协同作用。

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