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针对同基因SV40转化细胞产生的T淋巴细胞效应子介导的裂解作用的抗体阻断。

Antibody blockade of lysis by T lymphocyte effectors generated against syngeneic SV40 transformed cells.

作者信息

Gooding L R

出版信息

J Immunol. 1979 Jun;122(6):2328-36.

PMID:221583
Abstract

Antibody blockade of cell-mediated lysis was used to probe the cell surface structures recognized by T lymphocytes generated to syngeneic SV40 virus-transformed mouse cells. Alloantisera to H-2 antigens were highly effective in inhibiting lysis. Anti-H2 antibody blockade of lysis was haplotype specific even on transformed F1 target cells. Inhibition occurred only when antibody was bound to the target cell. Antibody binding to the effector did not inhibit lysis. Inhibition required that antibody be bound to the H-2 molecule itself; antibody to molecules associated with H-2, such as beta2-microglobulin, had no effect. Attempts to block lysis by using antisera to known virus-coded molecules were uniformly unsuccessful. These results are discussed in light of current controversy concerning the nature of the SV40 virus-specific transplantation antigen.

摘要

利用抗体阻断细胞介导的裂解作用,来探究针对同基因SV40病毒转化的小鼠细胞产生的T淋巴细胞所识别的细胞表面结构。针对H-2抗原的同种抗血清在抑制裂解方面非常有效。即使在转化的F1靶细胞上,抗H2抗体对裂解的阻断也是单倍型特异性的。只有当抗体与靶细胞结合时才会发生抑制作用。抗体与效应细胞的结合不会抑制裂解。抑制作用要求抗体与H-2分子本身结合;针对与H-2相关分子(如β2-微球蛋白)的抗体则没有作用。使用针对已知病毒编码分子的抗血清来阻断裂解的尝试均未成功。根据目前关于SV40病毒特异性移植抗原性质的争议对这些结果进行了讨论。

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