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脓胸相关性淋巴瘤患者的HLA - A等位基因:EB病毒潜伏抗原阳性淋巴瘤发生过程中的抗EB病毒宿主免疫反应

HLA-A alleles of patients with pyothorax-associated lymphoma: anti-Epstein-Barr virus (EBV) host immune responses during the development of EBV latent antigen-positive lymphomas.

作者信息

Kanno H, Ohsawa M, Hashimoto M, Iuchi K, Nakajima Y, Aozasa K

机构信息

Department of Pathology, Osaka University Medical School, Suita, Japan.

出版信息

Int J Cancer. 1999 Aug 27;82(5):630-4. doi: 10.1002/(sici)1097-0215(19990827)82:5<630::aid-ijc2>3.0.co;2-d.

DOI:10.1002/(sici)1097-0215(19990827)82:5<630::aid-ijc2>3.0.co;2-d
PMID:10417757
Abstract

Pyothorax-associated lymphoma (PAL) is an Epstein-Barr virus (EBV) latent antigen-positive lymphoma resembling EBV-transformed lymphoblastoid cell lines (LCLs) and develops in non-immunocompromised patients. Thus, deficient anti-viral-antigen immune responses might be involved in the development of PAL. As MHC class I-restricted cytotoxic T lymphocytes (CTLs) are the major constituent of anti-viral immune responses, the HLA allele type and its expression may affect the development of PAL. Flow-cytometric analyses of PAL cell lines and LCLs using the W6/32 monoclonal antibody revealed that expression of HLA class I varied among cell lines. Although one PAL cell line, OPL-2, exhibited low expression, an LCL and another PAL cell line, OPL-1, strongly expressed HLA class I. Among the EBV latent infection genes, EBV nuclear antigens 2, 3, 4 and 6 and latent membrane proteins can induce efficient CTL responses in combination with HLA-A2 or -A11. HLA-A alleles of PAL patients were determined using low-resolution PCR-based typing with HLA-A locus sequence-specific primer combinations. The antigen frequencies of HLA-A2 and -A11 in PAL patients were not significantly different from those in the normal Japanese population. Although HLA class I antigen should be expressed during the course of lymphomagenesis, no HLA-A alleles influenced the development of overt PALs.

摘要

脓胸相关淋巴瘤(PAL)是一种类似于EB病毒转化的淋巴母细胞系(LCL)的EB病毒(EBV)潜伏抗原阳性淋巴瘤,发生于非免疫功能低下的患者。因此,抗病毒抗原免疫反应缺陷可能参与了PAL的发生发展。由于MHC I类限制性细胞毒性T淋巴细胞(CTL)是抗病毒免疫反应的主要组成部分,HLA等位基因类型及其表达可能会影响PAL的发生发展。使用W6/32单克隆抗体对PAL细胞系和LCL进行流式细胞术分析发现,HLA I类的表达在不同细胞系中存在差异。虽然一个PAL细胞系OPL-2表达较低,但一个LCL和另一个PAL细胞系OPL-1强烈表达HLA I类。在EBV潜伏感染基因中,EBV核抗原2、3、4和6以及潜伏膜蛋白与HLA-A2或-A11结合可诱导有效的CTL反应。使用基于低分辨率PCR的HLA-A基因座序列特异性引物组合对PAL患者的HLA-A等位基因进行测定。PAL患者中HLA-A2和-A11的抗原频率与正常日本人群无显著差异。虽然HLA I类抗原在淋巴瘤发生过程中应该表达,但没有HLA-A等位基因影响显性PAL的发生发展。

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