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细胞毒性T淋巴细胞的体内分化。1. 免疫去胸腺(nu/nu)小鼠中的血清因子可分化CTL前体。

In vivo differentiation of cytotoxic T lymphocytes. 1. Serum factor in immunized athymic (nu/nu) mice could differentiate CTL precursor.

作者信息

Kamikaseda K, Taniguchi K, Nomoto K

出版信息

Immunobiology. 1984 Mar;166(2):212-8. doi: 10.1016/S0171-2985(84)80039-X.

Abstract

Mature cytotoxic T lymphocytes (CTLs) were hardly detected by 51Cr-release assay in the spleen of C3H/He mice after an intravenous injection of spleen cells of C57BL/6 (B6) mice. B6-specific CTL generation was augmented by transfer of sera obtained from C3H/He mice inoculated subcutaneously with EL-4 cells of B6 origin, P815 cells of DBA/2 origin or MH134 cells of C3H/HeN origin or these injected intraperitoneally with sheep or chicken erythrocytes. Such a factor can be produced also by athymic (nu/nu) mice. Such an augmentation of cytotoxicity was detected also in the regional lymph nodes after subcutaneous injection of allogeneic spleen cells. This factor may be different from augmenting factors reported already.

摘要

静脉注射C57BL/6(B6)小鼠的脾细胞后,在C3H/He小鼠的脾脏中通过51Cr释放试验几乎检测不到成熟的细胞毒性T淋巴细胞(CTL)。通过将皮下接种B6来源的EL-4细胞、DBA/2来源的P815细胞或C3H/HeN来源的MH134细胞的C3H/He小鼠的血清进行转移,或向这些小鼠腹腔注射绵羊或鸡红细胞,可以增强B6特异性CTL的产生。无胸腺(nu/nu)小鼠也能产生这种因子。在皮下注射同种异体脾细胞后的局部淋巴结中也检测到了这种细胞毒性的增强。这种因子可能与已报道的增强因子不同。

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