在对皮炎芽生菌的免疫中,T细胞亚群对CD40共刺激的不同需求。

Differential requirements of T cell subsets for CD40 costimulation in immunity to Blastomyces dermatitidis.

作者信息

Wüthrich Marcel, Fisette Phil L, Filutowicz Hanna I, Klein Bruce S

机构信息

Department of Pediatrics, University Hospital and Clinics, University of Wisconsin Medical School, 600 Highland Avenue, Madison, WI 53792, USA.

出版信息

J Immunol. 2006 May 1;176(9):5538-47. doi: 10.4049/jimmunol.176.9.5538.

Abstract

Cell-mediated immunity and production of type 1 cytokines are the main defenses against pathogenic fungi. Ligation of CD40 by CD40L on T cells is critical for the induction of these immune responses in vivo. We explored the role of CD40/CD40L interactions in vaccine immunity to Blastomyces dermatitidis by immunizing CD40(-/-) and CD40L(-/-) mice and analyzing their resistance to reinfection in a murine pulmonary model. In the absence of CD40 or CD40L, CD4(+) cells failed to get primed or produce type 1 cytokine and impaired the generation of CD8(+) T1 cells. The CD8(+) T cell defect was not due to regulatory T cells or impaired APC maturation or Ag presentation to T cells. If CD4(+) cells were first eliminated, vaccination of CD40(-/-) and CD40L(-/-) mice restored priming of CD8(+) cells, type 1 cytokine production, and resistance. Hence, CD4(+) and CD8(+) cells differ sharply in their requirement for CD40/CD40L interaction during the generation of antifungal immunity. Despite the plasticity of T cell subsets in vaccine immunity, in absence of CD40/CD40L interaction, CD4(+) cells may impede the priming of CD8(+) cells at the cost of host survival against a lethal infectious disease.

摘要

细胞介导的免疫和1型细胞因子的产生是抵御致病性真菌的主要防御机制。T细胞上的CD40L与CD40的结合对于体内诱导这些免疫反应至关重要。我们通过免疫CD40基因敲除(-/-)和CD40L基因敲除(-/-)小鼠,并在小鼠肺部模型中分析它们对再次感染的抵抗力,探讨了CD40/CD40L相互作用在针对皮炎芽生菌疫苗免疫中的作用。在缺乏CD40或CD40L的情况下,CD4⁺细胞无法被激活或产生1型细胞因子,并损害了CD8⁺T1细胞的生成。CD8⁺T细胞缺陷并非由于调节性T细胞或抗原呈递细胞(APC)成熟受损或抗原呈递给T细胞受损所致。如果首先清除CD4⁺细胞,对CD40基因敲除(-/-)和CD40L基因敲除(-/-)小鼠进行疫苗接种可恢复CD8⁺细胞的激活、1型细胞因子的产生和抵抗力。因此,在抗真菌免疫产生过程中,CD4⁺和CD8⁺细胞对CD40/CD40L相互作用的需求存在显著差异。尽管T细胞亚群在疫苗免疫中具有可塑性,但在缺乏CD40/CD40L相互作用的情况下,CD4⁺细胞可能会以宿主抵抗致命传染病的生存为代价,阻碍CD8⁺细胞的激活。

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