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在易感的BALB/c小鼠中建立对硕大利什曼原虫感染的抗性需要寄生虫特异性CD8 + T细胞。

Establishment of resistance to Leishmania major infection in susceptible BALB/c mice requires parasite-specific CD8+ T cells.

作者信息

Müller I, Pedrazzini T, Kropf P, Louis J, Milon G

机构信息

World Health Organization Immunology Research and Training Centre, University of Lausanne, Epalinges, Switzerland.

出版信息

Int Immunol. 1991 Jun;3(6):587-97. doi: 10.1093/intimm/3.6.587.

Abstract

Although CD4+ T cells are generally accepted to be responsible for the determination of resistance to infection in experimental murine cutaneous leishmaniasis, a contribution of CD8+ lymphocytes to immunity can be demonstrated under certain well-defined conditions. Normally highly susceptible BALB/c mice can be rendered resistant to infection with Leishmania major promastigotes by a single injection of monoclonal anti-CD4 antibodies at the beginning of infection. Mice treated in such a way can heal their primary cutaneous lesions and acquire immunity to subsequent challenge infection. Both the resolution of the primary infection and the induced state of immunity to reinfection in these mice is shown to be dependent upon the anti-leishmanial effector functions of CD8+ T cells. Furthermore, in contrast to control infected BALB/c mice, which are unable to mount a delayed-type hypersensitivity (DTH) response to viable parasites, mice cured as a result of treatment with anti-CD4 antibodies in vivo exhibit a strong DTH response, which can be significantly reduced by injection of either anti-CD4 or anti-CD8 monoclonal antibodies prior to antigenic challenge with viable promastigotes. Moreover, increased numbers of specific CD8+ T cells, able to transfer Leishmania-specific DTH responses, were found in lymphoid organs of BALB/c mice rendered resistant to infection by immunointervention with anti-CD4 monoclonal antibodies at the beginning of infection. Neutralization in vivo of interleukin 4 during the course of infection in BALB/c mice also enables these otherwise susceptible mice to resolve their cutaneous lesions and to decrease the parasite burden in infected tissues. CD8+ T cells are required for both of these beneficial effects. Taken together, these results indicate that in the immune BALB/c mouse, as in the normally resistant CBA mouse, CD8+ lymphocytes are involved in the elimination of L. major and in the establishment and maintenance of immunity against infection with this parasite.

摘要

尽管一般认为CD4+ T细胞在实验性小鼠皮肤利什曼病中负责决定对感染的抵抗力,但在某些明确界定的条件下,可以证明CD8+淋巴细胞对免疫有贡献。正常情况下高度易感的BALB/c小鼠在感染开始时单次注射单克隆抗CD4抗体后,可对硕大利什曼原虫前鞭毛体感染产生抗性。以这种方式处理的小鼠能够治愈其原发性皮肤病变,并获得对后续攻击感染的免疫力。这些小鼠原发性感染的消退以及对再感染的诱导免疫状态均显示依赖于CD8+ T细胞的抗利什曼效应功能。此外,与无法对活寄生虫产生迟发型超敏反应(DTH)的对照感染BALB/c小鼠不同,体内用抗CD4抗体治疗治愈的小鼠表现出强烈的DTH反应,在用活前鞭毛体进行抗原攻击之前注射抗CD4或抗CD8单克隆抗体可显著降低该反应。此外,在感染开始时通过抗CD4单克隆抗体免疫干预而对感染产生抗性的BALB/c小鼠的淋巴器官中,发现能够传递利什曼原虫特异性DTH反应的特异性CD8+ T细胞数量增加。在BALB/c小鼠感染过程中体内中和白细胞介素4也能使这些原本易感的小鼠治愈其皮肤病变并减少感染组织中的寄生虫负荷。这两种有益效果都需要CD8+ T细胞。综上所述,这些结果表明,在免疫的BALB/c小鼠中,如同在正常抗性的CBA小鼠中一样,CD8+淋巴细胞参与了硕大利什曼原虫的清除以及针对该寄生虫感染的免疫建立和维持。

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