Blanchard Nicolas, Gonzalez Federico, Schaeffer Marie, Joncker Nathalie T, Cheng Tiffany, Shastri Anjali J, Robey Ellen A, Shastri Nilabh
Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
Nat Immunol. 2008 Aug;9(8):937-44. doi: 10.1038/ni.1629. Epub 2008 Jun 29.
The parasite Toxoplasma gondii replicates in a specialized intracellular vacuole and causes disease in many species. Protection from toxoplasmosis is mediated by CD8(+) T cells, but the T. gondii antigens and host genes required for eliciting protective immunity are poorly defined. Here we identified GRA6, a polymorphic protein secreted in the parasitophorous vacuole, as the source of the immunodominant and protective decapeptide HF10 presented by the H-2L(d) major histocompatibility complex class I molecule. Presentation of the HF10-H-2L(d) ligand required proteolysis by ERAAP, the endoplasmic reticulum aminopeptidase associated with antigen processing. Consequently, expansion of protective CD8(+) T cell populations was impaired in T. gondii-infected ERAAP-deficient mice, which were more susceptible to toxoplasmosis. Thus, endoplasmic reticulum proteolysis is critical for eliciting protective immunity to a vacuolar parasite.
刚地弓形虫这种寄生虫在一种特殊的细胞内液泡中进行复制,并在许多物种中引发疾病。对弓形虫病的保护作用由CD8(+) T细胞介导,但引发保护性免疫所需的弓形虫抗原和宿主基因却鲜为人知。在此,我们鉴定出一种在寄生泡中分泌的多态性蛋白GRA6,它是由H-2L(d) 主要组织相容性复合体I类分子呈递的免疫显性和保护性十肽HF10的来源。HF10-H-2L(d) 配体的呈递需要内质网氨基肽酶ERAAP(与抗原加工相关的内质网氨基肽酶)进行蛋白水解。因此,在感染弓形虫的ERAAP缺陷小鼠中,保护性CD8(+) T细胞群体的扩增受到损害,这些小鼠对弓形虫病更易感。因此,内质网蛋白水解对于引发针对液泡寄生虫的保护性免疫至关重要。