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与位点特异性细胞毒性T淋巴细胞克隆Y-5共培养后,SV40 T抗原上免疫隐性细胞毒性T淋巴细胞决定簇V的丧失。

Loss of immunorecessive cytotoxic T lymphocyte determinant V on SV40 T antigen following cocultivation with site-specific cytotoxic T lymphocyte clone Y-5.

作者信息

Tanaka Y, Tevethia S S

机构信息

Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey 17033.

出版信息

Intervirology. 1990;31(2-4):197-202. doi: 10.1159/000150154.

Abstract

Five distinct antigenic sites recognized by cytotoxic T lymphocytes in H-2b mice have been identified on simian virus 40 (SV40) T antigen. Cocultivation of SV40-transformed cells with cytotoxic T lymphocyte (CTL) clones specific for epitopes I-IV results in the selection of variants which show a loss of either epitopes I, II, and III, II and III, or IV. We now report the isolation of a variant SV40-transformed cell line which has lost the expression of all five CTL epitopes on SV40 T antigen. These variant cells were no longer susceptible to lysis by CTL clones specific for all five epitopes. These variant cells would be used to relate alterations in SV40 T antigen structure with functional changes in the transformed cells.

摘要

在H - 2b小鼠中,细胞毒性T淋巴细胞所识别的猿猴病毒40(SV40)T抗原上的五个不同抗原位点已被确定。将SV40转化细胞与针对表位I - IV的细胞毒性T淋巴细胞(CTL)克隆共培养,会筛选出缺失表位I、II和III、II和III或IV的变体。我们现在报告分离出一种变体SV40转化细胞系,该细胞系在SV40 T抗原上失去了所有五个CTL表位的表达。这些变体细胞不再易被针对所有五个表位的CTL克隆裂解。这些变体细胞将用于关联SV40 T抗原结构的改变与转化细胞中的功能变化。

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