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通过转染编码这些抗原的基因来调节人胶质瘤细胞上MHC II类抗原的表达。

Expression of MHC class II antigens on human glioma cells modulated by transfection with genes encoding these antigens.

作者信息

Yoshida S, Takahashi H, Tanaka R

机构信息

Department of Neurosurgery, School of Medicine, Niigata University.

出版信息

Neurol Med Chir (Tokyo). 1991 Oct;31(10):623-8. doi: 10.2176/nmc.31.623.

Abstract

Four glioma cell lines not expressing human leukocyte antigen (HLA)-DR or DQ did so after transfection with genes encoding HLA-DR and DQ. The glioma cells had enhanced ability to stimulate allogeneic and autologous responding lymphocytes in the mixed lymphocyte response (MLR). Glioma cells expressing only HLA-DR had weaker MLR enhancement than those expressing both HLA-DR and DQ or only HLA-DQ. Stimulation by transformed glioma cells increased the killing activity of responding lymphocytes against autologous glioma cells 2.0 times. Both HLA-DR and DQ are important in MLR, and the immunogenicity of glioma cells might be increased by transfection with genes encoding these antigens.

摘要

四种不表达人类白细胞抗原(HLA)-DR或DQ的胶质瘤细胞系,在转染编码HLA-DR和DQ的基因后开始表达。这些胶质瘤细胞在混合淋巴细胞反应(MLR)中刺激同种异体和自体反应性淋巴细胞的能力增强。仅表达HLA-DR的胶质瘤细胞比同时表达HLA-DR和DQ或仅表达HLA-DQ的细胞具有较弱的MLR增强作用。转化的胶质瘤细胞刺激使反应性淋巴细胞对自体胶质瘤细胞的杀伤活性提高了2.0倍。HLA-DR和DQ在MLR中都很重要,转染编码这些抗原的基因可能会增加胶质瘤细胞的免疫原性。

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