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Cyclophosphamide-sensitive T lymphocytes suppress the in vivo generation of antigen-specific cytotoxic T lymphocytes

机译:对环磷酰胺敏感的T淋巴细胞可抑制体内抗原特异性细胞毒性T淋巴细胞的产生

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摘要

Murine T lymphocytes sensitized in vitro against either allogeneic lymphocytes or syngeneic hapten-conjugated lymphocytes do differentiate into highly effective cytotoxic T lymphocytes (CTL) (1-3). In vivo immunization of T lymphocytes to the same antigens, however, results in the generation of only marginal cytotoxic activity (1,4,5). Recently we found that the weakness of in vivo generated cytotoxicity is not due to a failure of antigen-induced T-cell sensitization but rather due to suppression of the in vivo differentiation of sensitized CTL precursors into effective CTL(6). In keeping with this finding it was postulated that suppressor cells may regulate the in vivo differentiation of CTL. We now report, that cyclophosphamide-sensitive T cells suppress the in vivo differentiation of antigen-specific CTL. Thus, pretreatment of mice with a single dose of cyclophosphamide (100 mg/kg) converts their state of low responsiveness to a state of high responsiveness.
机译:在体外对同种异体淋巴细胞或同基因半抗原结合的淋巴细胞致敏的小鼠T淋巴细胞确实可以分化为高效的细胞毒性T淋巴细胞(CTL)(1-3)。然而,T淋巴细胞对相同抗原的体内免疫仅导致边缘细胞毒活性的产生(1、4、5)。最近,我们发现体内产生的细胞毒性的弱点不是由于抗原诱导的T细胞敏化失败,而是由于抑制了敏化CTL前体在体内分化为有效CTL的作用(6)。与该发现一致,推测抑制细胞可以调节CTL的体内分化。我们现在报道,环磷酰胺敏感的T细胞抑制抗原特异性CTL的体内分化。因此,用单剂量的环磷酰胺(100 mg / kg)进行的小鼠预处理将其低响应状态转换为高响应状态。

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