Dieli F, Asherson G L, Sireci G, Dominici R, Sciré E, Salerno A
Institute of General Pathology, University of Palermo, ISMEDA-CNR, Italy.
J Immunol. 1997 Mar 15;158(6):2567-75.
This paper describes the development of Ag-specific proliferation and the production of IFN-gamma and IL-2 during contact sensitivity (CS) to the hapten picryl chloride (PCl). Lymph node cells from mice immunized with PCl proliferate and produce IFN-gamma and IL-2 when re-exposed to the specific Ag in vitro. Time course experiments showed that the peak IFN-gamma production occurred at days 3 and 4 after immunization, with a sharp decline by day 6. In contrast, proliferation and IL-2 production peaked at day 3 but persisted up to day 10. Proliferation and IFN-gamma and IL-2 production displayed by immune lymph node cells were Ag-specific but required different cell populations. In fact, the production of IFN-gamma was due to a CD8+, gamma delta+ T cell, while proliferation and IL-2 production required the presence of a CD4+, alpha beta+ T cell. Furthermore, IFN-gamma production showed genetic (MHC) restriction, and finer analysis using congenic strains of mice indicated that the K molecule was the restricting element. This was confirmed by blocking the K molecule of the APC used to trigger IFN-gamma production with a specific mAb. In contrast, proliferation and IL-2 production were I-A-restricted, as demonstrated using congenic strains of mice and blocking the I-A molecule of the APCs. Further analysis using purified gamma delta+ cells revealed that these cells produced IFN-gamma in an Ag-specific and MHC (K)-restricted fashion. Injection of mice with a mAb to IL-2 blocked subsequent in vitro proliferation, as well as IL-2 and IFN-gamma production, while all three in vitro responses were unaffected by injection of a mAb to IFN-gamma given at the time of immunization. Furthermore, injection of mice with a mAb to IL-2 blocked the CS reaction when given at the time of immunization, while it had no effect when given at the time of challenge. Injection of mice with mAb to IFN-gamma at the time of challenge reduced but did not abolished CS, suggesting that IFN-gamma is important but not exclusively responsible for the CS reaction.
本文描述了在对卤化苦味酸(PCl)的接触性敏感反应(CS)过程中,抗原特异性增殖以及γ干扰素(IFN-γ)和白细胞介素-2(IL-2)的产生情况。用PCl免疫的小鼠的淋巴结细胞在体外再次接触特异性抗原时会增殖并产生IFN-γ和IL-2。时间进程实验表明,IFN-γ产生的峰值出现在免疫后第3天和第4天,到第6天急剧下降。相比之下,增殖和IL-2产生的峰值出现在第3天,但一直持续到第10天。免疫淋巴结细胞所表现出的增殖以及IFN-γ和IL-2的产生具有抗原特异性,但需要不同的细胞群体。实际上,IFN-γ的产生归因于CD8⁺、γδ⁺T细胞,而增殖和IL-2的产生需要CD4⁺、αβ⁺T细胞的存在。此外,IFN-γ的产生表现出遗传(主要组织相容性复合体,MHC)限制性,使用同源近交系小鼠进行的更精细分析表明,K分子是限制性元件。用特异性单克隆抗体阻断用于触发IFN-γ产生的抗原呈递细胞(APC)的K分子证实了这一点。相比之下,如使用同源近交系小鼠并阻断APC的I-A分子所证明的,增殖和IL-2的产生受I-A限制。使用纯化的γδ⁺细胞进行的进一步分析表明,这些细胞以抗原特异性和MHC(K)限制性方式产生IFN-γ。给小鼠注射抗IL-2单克隆抗体可阻断随后的体外增殖以及IL-2和IFN-γ的产生,而在免疫时注射抗IFN-γ单克隆抗体对所有这三种体外反应均无影响。此外,在免疫时给小鼠注射抗IL-2单克隆抗体可阻断CS反应,而在激发时注射则无作用。在激发时给小鼠注射抗IFN-γ单克隆抗体可使CS反应减弱但并未消除,这表明IFN-γ很重要,但并非CS反应的唯一原因。