Lang Thierry, Courret Nathalie, Colle Jean-Hervé, Milon Geneviève, Antoine Jean-Claude
Unité d'Immunophysiologie et Parasitisme Intracellulaire, Institut Pasteur, Paris, France.
Infect Immun. 2003 May;71(5):2674-83. doi: 10.1128/IAI.71.5.2674-2683.2003.
The production of cytokines by CD4 lymph node T lymphocytes derived from BALB/c mice recently infected in the ear dermis with high (10(6) parasites) or low (10(3) parasites) doses of Leishmania major metacyclic promastigotes (MP) was examined over a 3-week period following inoculation. Results were compared with those obtained when mice were injected with less infectious parasite populations, namely, stationary-phase or log-phase promastigotes (LP). Cells were purified 16 h and 3, 8, and 19 days after inoculation, and the amounts of gamma interferon (IFN-gamma) and interleukin-4 (IL-4) released in response to LACK (Leishmania homolog of receptors for activated C kinase) or total L. major antigens were assessed. We found that LACK-reactive T cells from mice inoculated with a high dose of parasites first produced IFN-gamma and later on IL-4; the level of IFN-gamma produced early by these cells was dependent upon the stage of the promastigotes inoculated, the highest level being reached with cells recovered from mice inoculated with the least infectious parasites, LP; sequential production of IFN-gamma and then of IL-4 also characterized L. major antigen-reactive CD4 T cells, suggesting that the early production of IFN-gamma does not impede the subsequent rise of IL-4 and finally the expansion of the parasites; after low-dose inoculation of MP, cutaneous lesions developed with kinetics similar to that of lesions induced after inoculation of 10(6) LP, but in this case CD4 T lymphocytes did not release IFN-gamma or IL-4 in the presence of LACK and neither cytokine was produced in response to L. major antigens before the onset of lesion signs. These results suggest the existence of a discreet phase in terms of CD4 T-cell reactivity for at least the first 8 days following inoculation, a time period during which parasites are able to grow moderately. In conclusion, the levels and profiles of cytokines produced by Leishmania-specific CD4 T lymphocytes clearly depend on both the stage of differentiation and number of parasites used for inoculation.
对接种后3周内,来自近期在耳部真皮层感染高剂量(10⁶个寄生虫)或低剂量(10³个寄生虫)硕大利什曼原虫循环前鞭毛体(MP)的BALB/c小鼠的CD4淋巴结T淋巴细胞产生细胞因子的情况进行了检测。将结果与给小鼠注射传染性较低的寄生虫群体(即静止期或对数期前鞭毛体,LP)时获得的结果进行比较。在接种后16小时以及3、8和19天对细胞进行纯化,并评估针对LACK(活化C激酶受体的利什曼原虫同源物)或总硕大利什曼原虫抗原释放的γ干扰素(IFN-γ)和白细胞介素-4(IL-4)的量。我们发现,接种高剂量寄生虫的小鼠中对LACK有反应的T细胞首先产生IFN-γ,随后产生IL-4;这些细胞早期产生的IFN-γ水平取决于接种的前鞭毛体阶段,从接种传染性最低的寄生虫(LP)的小鼠中回收的细胞达到的水平最高;IFN-γ随后IL-4的顺序产生也是硕大利什曼原虫抗原反应性CD4 T细胞的特征,这表明IFN-γ的早期产生并不妨碍随后IL-4的升高以及最终寄生虫的增殖;低剂量接种MP后,皮肤病变的发展动力学与接种10⁶个LP后诱导的病变相似,但在这种情况下,CD4 T淋巴细胞在LACK存在下不释放IFN-γ或IL-4,并且在病变体征出现之前,两种细胞因子均不响应硕大利什曼原虫抗原而产生。这些结果表明,至少在接种后的前8天,就CD4 T细胞反应性而言存在一个离散阶段,在此期间寄生虫能够适度生长。总之,利什曼原虫特异性CD4 T淋巴细胞产生的细胞因子水平和谱明显取决于分化阶段和用于接种的寄生虫数量。