组织胞浆
组织胞浆菌病
微生物学
生物
免疫
免疫系统
免疫学
体外
病原真菌
真菌
病毒学
荚膜组织胞浆菌
生物化学
植物
作者
Eszter Lázár‐Molnár,Attila Gácser,Gordon J. Freeman,Steven C. Almo,Stanley G. Nathenson,Joshua D. Nosanchuk
标识
DOI:10.1073/pnas.0711918105
摘要
The PD-1 costimulatory receptor inhibits T cell receptor signaling upon interacting with its ligands PD-L1 and PD-L2. The PD-1/PD-L pathway is critical in maintaining self-tolerance. In this study, we examined the role of PD-1 in a mouse model of acute infection with Histoplasma capsulatum , a major human pathogenic fungus. In a lethal model of histoplasmosis, all PD-1-deficient mice survived infection, whereas the wild-type mice died with disseminated disease. PD-L expression on macrophages and splenocytes was up-regulated during infection, and macrophages from infected mice inhibited in vitro T cell activation. Of interest, antibody blocking of PD-1 significantly increased survival of lethally infected wild-type mice. Thus, our studies extend the role of the PD-1/PD-L pathway in regulating antimicrobial immunity to fungal pathogens. The results show that the PD-1/PD-L pathway has a key role in the regulation of antifungal immunity, and suggest that manipulation of this pathway represents a strategy of immunotherapy for histoplasmosis.
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