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MHC II类抗原的新作用:有证据表明其对肿瘤细胞具有保护作用,可抵抗自然杀伤细胞和淋巴因子激活的杀伤细胞的细胞毒性。

A novel role for MHC class II antigens: evidence implicating a protective effect on tumour cells against cytotoxicity by NK and LAK cells.

作者信息

Lobo P I, Patel H C

机构信息

Department of Internal Medicine, University of Virginia School of Medicine, Charlottesville.

出版信息

Immunology. 1994 Oct;83(2):240-4.

Abstract

There are several lines of evidence clearly demonstrating that major histocompatibility complex (MHC) class I antigens are important in protecting haemopoietic tumour cells from natural killer (NK)-mediated cell lysis. In the present studies we examined the role of MHC class II antigens in affording such protection to haemopoietic tumour cell lines. NK and lymphokine-activated killer (LAK) lysis were performed on two human B lymphoma cell lines and their mutants lacking HLA class II expression, i.e. DR, DP and DQ. Raji and T5-1 were compared to their mutants RM3 and 6.1.6, respectively. Significantly more lysis was observed with the mutants compared to the parent cell line. Effectors used included (1) peripheral blood NK effectors, (2) a human NK cell line (NK 3.3), and (3) peripheral blood LAK effectors. The increased lysis with the mutants could not be explained on the basis of (1) increased conjugate formation, (2) increased cell fragility or (3) ineffectual expression of HLA class I and other non-HLA antigens. These findings suggest that HLA class II molecules may have a novel role. They may be relevant not only in antigen presentation but may also protect tumour cells (and possibly normal activated lymphoid cells) against lysis mediated by NK and LAK cells.

摘要

有几条证据清楚地表明,主要组织相容性复合体(MHC)I类抗原在保护造血肿瘤细胞免受自然杀伤(NK)细胞介导的细胞裂解方面很重要。在本研究中,我们研究了MHC II类抗原在为造血肿瘤细胞系提供这种保护中的作用。对两个人类B淋巴瘤细胞系及其缺乏HLA II类表达(即DR、DP和DQ)的突变体进行了NK和淋巴因子激活的杀伤(LAK)裂解实验。分别将Raji和T5-1与其突变体RM3和6.1.6进行比较。与亲本细胞系相比,突变体的裂解明显更多。所用的效应细胞包括:(1)外周血NK效应细胞,(2)人NK细胞系(NK 3.3),以及(3)外周血LAK效应细胞。突变体裂解增加不能基于以下原因来解释:(1)结合物形成增加,(2)细胞脆性增加,或(3)HLA I类及其他非HLA抗原的无效表达。这些发现表明HLA II类分子可能具有新的作用。它们可能不仅与抗原呈递有关,还可能保护肿瘤细胞(以及可能的正常活化淋巴细胞)免受NK和LAK细胞介导的裂解。

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