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主要组织相容性复合体(MHC)II类缺陷综合征中干扰素诱导的II类主要组织相容性抗原表达。

Interferon-induced expression of class II major histocompatibility antigens in the major histocompatibility complex (MHC) class II deficiency syndrome.

作者信息

Plaeger-Marshall S, Haas A, Clement L T, Giorgi J V, Chen I S, Quan S G, Gatti R A, Stiehm E R

机构信息

Department of Pediatrics, UCLA School of Medicine, Los Angeles, California 90024.

出版信息

J Clin Immunol. 1988 Jul;8(4):285-95. doi: 10.1007/BF00916557.

Abstract

Class II antigens encoded by genes of the major histocompatibility complex (MHC) are expressed by a variety of cell types and have a vital role in the cellular interactions required for an effective immune response. We have analyzed the regulation of HLA-DR, DP, and DQ class II antigen expression on cells of different lineage from an immunodeficient patient with the MHC class II deficiency syndrome. T and B lymphocytes, monocytes, and fibroblasts, which initially expressed no class II antigens, were treated with inductive stimuli that normally lead to enhanced expression of class II antigens. Monocytes, but not fibroblasts, cultured for 48-96 hr in the presence of recombinant gamma interferon expressed all three types of class II antigens. In contrast, T lymphocytes did not express class II antigens following their exposure to a variety of stimuli, including activation with phytohemagglutinin and culture in the presence of interleukin-2, transformation by the retrovirus HTLV-1 or HTLV-2, or exposure to the demethylating agent 5-azacytidine. Similarly, class II antigens were not induced on B cells by cross-linkage of surface immunoglobulin molecules with anti-mu, exposure to Epstein-Barr virus, or treatment with soluble factors secreted by activated T cells. These results demonstrate that the regulation of class II MHC antigen expression by monocytes and lymphocytes is dissimilar and suggest that different regulatory genes are involved in the control of class II antigen expression by cells of different lineage.

摘要

主要组织相容性复合体(MHC)基因编码的II类抗原由多种细胞类型表达,并且在有效免疫反应所需的细胞相互作用中起着至关重要的作用。我们分析了来自一名患有MHC II类缺陷综合征的免疫缺陷患者不同谱系细胞上HLA - DR、DP和DQ II类抗原表达的调控情况。最初不表达II类抗原的T淋巴细胞、B淋巴细胞、单核细胞和成纤维细胞,用通常会导致II类抗原表达增强的诱导刺激进行处理。在重组γ干扰素存在的情况下培养48 - 96小时,单核细胞而非成纤维细胞表达了所有三种类型的II类抗原。相比之下,T淋巴细胞在暴露于多种刺激后并未表达II类抗原,这些刺激包括用植物血凝素激活并在白细胞介素 - 2存在下培养、被逆转录病毒HTLV - 1或HTLV - 2转化,或暴露于去甲基化剂5 - 氮杂胞苷。同样,通过用抗μ交联表面免疫球蛋白分子、暴露于爱泼斯坦 - 巴尔病毒或用活化T细胞分泌的可溶性因子处理,也不会在B细胞上诱导出II类抗原。这些结果表明,单核细胞和淋巴细胞对II类MHC抗原表达的调控是不同的,并且提示不同的调控基因参与了不同谱系细胞对II类抗原表达的控制。

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