Fishwild D M, Benike C J, Engleman E G
Stanford Medical School Blood Center, CA.
J Immunol. 1988 Mar 15;140(6):1994-8.
MHC-restricted, viral Ag-specific "memory" CTL are thought to play a decisive role in the defense against pathogenic viruses. However, the requirements for activating such CTL remain controversial. In particular, the role of CD4+ helper cells and their soluble products (e.g., IL-2) are uncertain. To approach these questions as they relate to EBV-specific CTL, highly purified CD8+ T cells from healthy EBV-seropositive individuals were cultured with autologous irradiated EBV-transformed B lymphoblastoid cell lines (LCL), in the presence or absence of autologous CD4+ cells or 1 to 10 U/ml purified rIL-2. The results indicate that the induction of CTL requires neither Th cells nor exogenous IL-2. The CTL generated from isolated CD8+ cells were HLA class I restricted as demonstrated by their ability to lyse targets sharing at least one HLA-A or -B Ag with the stimulating autologous LCL. Furthermore, a mAb (W6/32) to a common determinant on HLA class I Ag blocked both the generation and effector phases of killing, whereas an HLA class II directed mAb had no effect. Addition of an IL-2R-specific antibody (anti-Tac) to the culture medium blocked induction of CTL, suggesting that endogenously produced IL-2 plays an obligatory role in this system. Paraformaldehyde fixation of LCL abrogated their ability to function as stimulator cells; however, addition of 2 U/ml exogenous IL-2 to fixed LCL cultured with CD8+ cells allowed for the induction of highly specific CTL. These results indicate that EBV-specific memory CTL can be activated in the absence of CD4+ helper cells or their soluble products, but nonetheless require Ag and IL-2.
MHC 限制的、病毒抗原特异性的“记忆”CTL 被认为在抵御致病性病毒中起决定性作用。然而,激活此类 CTL 的条件仍存在争议。特别是,CD4 +辅助细胞及其可溶性产物(如 IL-2)的作用尚不确定。为了探讨与 EBV 特异性 CTL 相关的这些问题,将来自健康 EBV 血清阳性个体的高度纯化的 CD8 + T 细胞与自体照射的 EBV 转化的 B 淋巴母细胞系(LCL)一起培养,同时存在或不存在自体 CD4 +细胞或 1 至 10 U/ml 的纯化重组人白细胞介素 -2(rIL-2)。结果表明,CTL 的诱导既不需要 Th 细胞也不需要外源性 IL-2。从分离的 CD8 +细胞产生的 CTL 受 HLA I 类限制,这通过它们裂解与刺激自体 LCL 共享至少一种 HLA-A 或 -B 抗原的靶标的能力得以证明。此外,针对 HLA I 类抗原共同决定簇的单克隆抗体(W6/32)阻断了杀伤的产生和效应阶段,而针对 HLA II 类的单克隆抗体则没有影响。向培养基中添加 IL-2R 特异性抗体(抗 Tac)阻断了 CTL 的诱导,表明内源性产生的 IL-2 在该系统中起必要作用。LCL 的多聚甲醛固定消除了它们作为刺激细胞的功能;然而,向与 CD8 +细胞一起培养的固定 LCL 中添加 2 U/ml 的外源性 IL-2 可诱导产生高度特异性的 CTL。这些结果表明,EBV 特异性记忆 CTL 可以在没有 CD4 +辅助细胞或其可溶性产物的情况下被激活,但仍然需要抗原和 IL-2。