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对细胞介导的细胞毒性的抗性与AKR白血病中H-2K基因产物的减少相关。

Resistance to cell-mediated cytotoxicity is correlated with reduction of H-2K gene products in AKR leukemia.

作者信息

Schmidt W, Festenstein H

出版信息

Immunogenetics. 1982;16(3):257-64. doi: 10.1007/BF00343314.

Abstract

AKR leukemia cell lines differing in the amount of H-2K and H-2D antigens expressed on the cell surface were used to assess cell-mediated immune responses in syngeneic mice against Gross/AKR murine leukemia virus (MuLV)-induced tumors. Leukemic cells with reduced expression of H-2Kk antigens were inactive as inducers of Gross-MuLV/H-2k-specific cytotoxic T lymphocytes (CTL) and resistant to lysis by CTL raised against H-2Kk positive AKR leukemia cells. H-2Kk positive leukemias induced cytotoxic effectors, which upon restimulation in vitro, lysed the stimulating and other H-2Kk positive leukemia cells. In antibody inhibition experiments, T-cell-mediated cytotoxicity to these leukemias could only be inhibited by antisera and monoclonal antibodies specific for the H-2Kk antigens. Due to this specific role of H-2Kk antigens in T-cell cytotoxicity to Gross/AKR MuLV-induced tumors, reduced expression of H-2Kk antigens on spontaneous AKR leukemic cells could have important implications for surveillance of these neoplastic cells.

摘要

利用在细胞表面表达的H-2K和H-2D抗原量不同的AKR白血病细胞系,评估同基因小鼠针对格罗斯/AKR鼠白血病病毒(MuLV)诱导的肿瘤的细胞介导免疫反应。H-2Kk抗原表达降低的白血病细胞作为格罗斯-MuLV/H-2k特异性细胞毒性T淋巴细胞(CTL)的诱导剂无活性,并且对针对H-2Kk阳性AKR白血病细胞产生的CTL的裂解具有抗性。H-2Kk阳性白血病诱导细胞毒性效应物,在体外再次刺激时,这些效应物会裂解刺激细胞和其他H-2Kk阳性白血病细胞。在抗体抑制实验中,对这些白血病的T细胞介导的细胞毒性只能被针对H-2Kk抗原的抗血清和单克隆抗体抑制。由于H-2Kk抗原在T细胞对格罗斯/AKR MuLV诱导的肿瘤的细胞毒性中具有这种特定作用,自发AKR白血病细胞上H-2Kk抗原表达的降低可能对这些肿瘤细胞的监测具有重要意义。

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