Ostrowski Mario A, Yu Qigui, Yue Feng Yun, Liu Jun, Jones Brad, Gu Xiao X, Loutfy Mona, Kovacs Colin M, Halpenny Roberta
Department of Immunology, University of Toronto, Toronto, Canada. m.ostrowski:@utoronto.ca
Immunol Res. 2006;35(1-2):89-102. doi: 10.1385/IR:35:1:89.
Globally, at least 60 million people have been infected with the human immunodeficiency virus type 1 (HIV-1), the majority of whom will develop the acquired immunodeficiency syndrome (AIDS) leading to tremendous morbidity and the mortality. Understanding the immunopathogenesis of AIDS and the immune correlates of viral protection are necessary to develop effective vaccines and immunotherapies. A major focus of our laboratory has been to understand the CD4+ T cell immune response directed against HIV- 1, and to determine mechanisms of T cell dysfunction that lead to viral escape. In addition, we are interested in evaluating the TNF-TNFR family members as potential molecular adjuvants that could be incorporated into vaccines which could be used to further boost T cell immunogenicity in healthy or HIV-1-infected individuals, as many of these molecules have been shown to replace the functions of CD4+ T cell help.
在全球范围内,至少有6000万人感染了1型人类免疫缺陷病毒(HIV-1),其中大多数人会发展为获得性免疫缺陷综合征(AIDS),导致巨大的发病率和死亡率。了解AIDS的免疫发病机制以及病毒保护的免疫相关因素对于开发有效的疫苗和免疫疗法至关重要。我们实验室的一个主要重点是了解针对HIV-1的CD4+ T细胞免疫反应,并确定导致病毒逃逸的T细胞功能障碍机制。此外,我们有兴趣评估TNF-TNFR家族成员作为潜在的分子佐剂,这些佐剂可纳入疫苗中,用于进一步增强健康个体或HIV-1感染个体的T细胞免疫原性,因为许多这些分子已被证明可替代CD4+ T细胞辅助功能。