Khan I A, Kasper L H
Department of Medicine, Dartmouth Medical School, Hanover, NH 03755, USA.
J Immunol. 1996 Sep 1;157(5):2103-8.
Cytokines of the Th1 profile are important mediators of protective host immunity against Toxoplasma gondii infection in mice. In this study we describe the effect of the recently identified cytokine, IL-15, on prevention of murine infection with T. gondii. Administration of exogenous rIL-15 with soluble Toxoplasma lysate Ag (TLA) provides complete protection against a lethal parasite challenge, whereas treatment with either rIL-15 or TLA alone is not protective. Following immunization with TLA/rIL-15, there is a significant proliferation of splenocytes expressing the CD8+ phenotype in response to TLA. A significant rise in the level of serum IFN gamma was observed in vaccinated mice. Adoptive transfer of CD8+ T cells, but not CD4+ T cells, from TLA/rIL-15-vaccinated mice protects naive mice from a lethal parasite challenge. These CD8+ T cells exhibit enhanced CTL activity against target macrophages infected with T. gondii. Mice that have been immunized are protected against lethal parasite challenge for at least 1 mo postvaccination. These observations demonstrate that TLA when administered with exogenous rIL-15 generates toxoplasmacidal Ag-specific CD8+ T cells. These T cells proliferate upon exposure to parasite Ag, exhibit long term memory CTL against infected target cells, and may be involved in host immune memory to this parasite.
Th1型细胞因子是小鼠抵抗刚地弓形虫感染的保护性宿主免疫的重要介质。在本研究中,我们描述了最近鉴定出的细胞因子IL-15对预防小鼠感染刚地弓形虫的作用。将外源性重组IL-15与可溶性弓形虫裂解物抗原(TLA)一起给药可提供完全保护,使其免受致命性寄生虫攻击,而单独用重组IL-15或TLA治疗则无保护作用。用TLA/重组IL-15免疫后,表达CD8+表型的脾细胞对TLA有显著增殖反应。在接种疫苗的小鼠中观察到血清IFNγ水平显著升高。从用TLA/重组IL-15接种疫苗的小鼠中过继转移CD8+T细胞,而不是CD4+T细胞,可保护未免疫小鼠免受致命性寄生虫攻击。这些CD8+T细胞对感染刚地弓形虫的靶巨噬细胞表现出增强的CTL活性。免疫后的小鼠在接种疫苗后至少1个月内可免受致命性寄生虫攻击。这些观察结果表明,TLA与外源性重组IL-15一起给药时可产生杀弓形虫抗原特异性CD8+T细胞。这些T细胞在接触寄生虫抗原后增殖,对感染的靶细胞表现出长期记忆CTL,并且可能参与宿主对这种寄生虫的免疫记忆。