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慢性乙型肝炎患者中乙肝病毒DNA转染的骨髓瘤细胞特异性细胞毒性T细胞

Hepatitis B virus-DNA transfected myeloma cell-specific cytotoxic T cells in chronic hepatitis B patients.

作者信息

Kamogawa Y, Yamauchi K, Obata H, Chisaka O, Matsubara K

机构信息

Division of Medicine, Tokyo Women's Medical College, Japan.

出版信息

Virology. 1992 Nov;191(1):321-6. doi: 10.1016/0042-6822(92)90194-t.

Abstract

To study the mechanisms of hepatitis B virus (HBV)-induced chronic hepatitis (B-CH), we took chronic hepatitis B patients' peripheral blood lymphocytes (PBL) and examined their cytotoxic activities against human myeloma cells (ARH77) transfected by HBV-DNA. Two different transfected cells, one expressing HBV envelope antigens (S6) and the other expressing HBV core antigens (C4), were prepared and used as targets in the in vitro cytotoxic test. We found that PBL of B-CH patients had specific cytotoxic activity against these target cells (S6, 22.0 +/- 4.8%; C4, 21.6 +/- 4.8%), whereas no remarkable cytotoxic activity was observed in non-B chronic hepatitis patients as well as asymptomatic chronic HBV carriers. These specific cytotoxic activities were inhibited with anti-CD3 antibody, hence these killer cells belonged to T cells (cytotoxic T cells; CTL). The requirement of HLA class 1 antigens to exert these CTL activities was demonstrated by the absence of CTL activity with PBL obtained from HLA-nonidentical B-CH patients and by the inhibition of their activities with anti-HLA class 1 antibody. Thus, our results indicate that, at least two different CTL, one recognizing envelop antigen and the other recognizing core antigen, exist in chronic hepatitis B patients.

摘要

为研究乙型肝炎病毒(HBV)诱导的慢性肝炎(B-CH)的发病机制,我们采集了慢性乙型肝炎患者的外周血淋巴细胞(PBL),并检测其对转染了HBV-DNA的人骨髓瘤细胞(ARH77)的细胞毒活性。制备了两种不同的转染细胞,一种表达HBV包膜抗原(S6),另一种表达HBV核心抗原(C4),并将其用作体外细胞毒试验的靶细胞。我们发现,B-CH患者的PBL对这些靶细胞具有特异性细胞毒活性(S6为22.0±4.8%;C4为21.6±4.8%),而非B型慢性肝炎患者以及无症状慢性HBV携带者未观察到明显的细胞毒活性。这些特异性细胞毒活性被抗CD3抗体抑制,因此这些杀伤细胞属于T细胞(细胞毒性T细胞;CTL)。从HLA不匹配的B-CH患者获得的PBL缺乏CTL活性以及抗HLA-Ⅰ类抗体对其活性的抑制,证明了发挥这些CTL活性需要HLA-Ⅰ类抗原。因此,我们的结果表明,慢性乙型肝炎患者中至少存在两种不同的CTL,一种识别包膜抗原,另一种识别核心抗原。

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