Huston D P, Steinberg A D
J Exp Med. 1980 Sep 1;152(3):748-53. doi: 10.1084/jem.152.3.748.
Cytotoxic lymphocyte (CTL) responses of unprimed NZB spleen cells peaked on day 4 of culture as did cells from primed NZB or BALB/c mice. In contrast, primary BALB/c and DBA/2 responses peaked on day 6 of culture. Thus, NZB CTL generation was similar to the accelerated in vitro generation of CTL from the spleen cells of alloantigen-primed NZB and BALB/c mice. To evaluate the kinetics of these CTL responses, multiple-time-point analyses were performed during the initial 90 min of the 51Cr-release assays. Analyses were done on days 4 and 6. On day 4, NZB CTL had an initial velocity of lysis slightly greater than that of BALB/c or DBA/2 CTL; however, it was far less than that of secondary NZB and secondary BALB/c CTL. These studies indicate that NZB mice can generate primary CTL responses at an accelerated rate. Such augmented primary responses are unique and may explain recently described abnormal NZB T cell recognition as well as resistance of NZB CTL to suppressor signals.
未致敏的新西兰黑鼠(NZB)脾细胞的细胞毒性淋巴细胞(CTL)反应在培养第4天达到峰值,致敏的NZB或BALB/c小鼠的细胞也是如此。相比之下,BALB/c和DBA/2的初次反应在培养第6天达到峰值。因此,NZB的CTL生成类似于从同种抗原致敏的NZB和BALB/c小鼠脾细胞体外加速生成CTL。为了评估这些CTL反应的动力学,在51Cr释放试验的最初90分钟内进行了多个时间点分析。分析在第4天和第6天进行。在第4天,NZB的CTL初始裂解速度略高于BALB/c或DBA/2的CTL;然而,远低于二次免疫的NZB和二次免疫的BALB/c的CTL。这些研究表明,NZB小鼠能够以加速的速度产生初次CTL反应。这种增强的初次反应是独特的,可能解释了最近描述的NZB T细胞识别异常以及NZB的CTL对抑制信号的抗性。