Fujiwara H, Levy R B, Shearer G M, Terry W D
J Immunol. 1979 Jul;123(1):423-5.
A comparison was made of the effects of i.v. inoculation of trinitrophenyl-(TNP) conjugated syngeneic cells on the subsequent in vitro generation of TNP-reactive effector cell activity and on the in vivo development of TNP-contact sensitivity. The administration of syngeneic TNP-conjugated spleen cells before 2,4,6-trinitro-1-chlorobenzene (TNCB) painting abolished the capability of animals to develop TNP-contact sensitivity. In contrast, the same treatment resulted in an appreciable augmentation in the generation of TNP-reactive cytotoxic effector cell activity as measured by subsequent in vitro sensitization with TNP-conjugated cells. The possible mechanisms by which enhanced TNP-reactive cytotoxic effector cell activity was elicited under conditions identical to those that induced unresponsiveness for TNP-contact sensitivity are discussed.
对静脉注射三硝基苯基 -(TNP)偶联的同基因细胞对随后TNP反应性效应细胞活性的体外生成以及对TNP接触敏感性的体内发展的影响进行了比较。在涂抹2,4,6 - 三硝基 - 1 - 氯苯(TNCB)之前给予同基因TNP偶联的脾细胞消除了动物产生TNP接触敏感性的能力。相反,相同的处理导致通过随后用TNP偶联细胞进行体外致敏测量的TNP反应性细胞毒性效应细胞活性的产生有明显增强。讨论了在与诱导TNP接触敏感性无反应性相同的条件下引发增强的TNP反应性细胞毒性效应细胞活性的可能机制。