Department of Medicine, Mekelle University College of Health Sciences, Mekelle, Ethiopia.
Department of Global Health, Kenyan Medical Research Institute (KEMRI) - Wellcome Research Programme, Nairobi, Kenya.
Front Immunol. 2021 Jun 17;12:693269. doi: 10.3389/fimmu.2021.693269. eCollection 2021.
Chronic immune activation has been considered as the driving force for CD4 T cell depletion in people infected with HIV-1. Interestingly, the normal immune profile of adult HIV-negative individuals living in Africa also exhibit chronic immune activation, reminiscent of that observed in HIV-1 infected individuals. It is characterized by increased levels of soluble immune activation markers, such as the cytokines interleukin (IL)-4, IL-10, TNF-α, and cellular activation markers including HLA-DR, CD-38, CCR5, coupled with reduced naïve and increased memory cells in CD4 and CD8 subsets. In addition, it is accompanied by low CD4 T cell counts when compared to Europeans. There is also evidence that mononuclear cells from African infants secrete less innate cytokines than South and North Americans and Europeans . Chronic immune activation in Africans is linked to environmental factors such as parasitic infections and could be responsible for previously observed immune hypo-responsiveness to infections and vaccines. It is unclear whether the immunogenicity and effectiveness of anti-SARS-CoV-2 vaccines will also be reduced by similar mechanisms. A review of studies investigating this phenomenon is urgently required as they should inform the design and delivery for vaccines to be used in African populations.
慢性免疫激活被认为是导致 HIV-1 感染者 CD4 T 细胞耗竭的驱动力。有趣的是,生活在非洲的 HIV 阴性成年人的正常免疫特征也表现出慢性免疫激活,这让人联想到 HIV-1 感染者的情况。其特征是可溶性免疫激活标志物水平升高,如细胞因子白细胞介素(IL)-4、IL-10、TNF-α,以及细胞活化标志物包括 HLA-DR、CD-38、CCR5,同时 CD4 和 CD8 亚群中的幼稚细胞减少,记忆细胞增加。此外,与欧洲人相比,其 CD4 T 细胞计数也较低。还有证据表明,与南、北美洲和欧洲人相比,非洲婴儿的单核细胞分泌的先天细胞因子较少。非洲的慢性免疫激活与寄生虫感染等环境因素有关,可能是导致先前观察到的对感染和疫苗的免疫反应低下的原因。目前尚不清楚抗 SARS-CoV-2 疫苗的免疫原性和有效性是否也会因类似机制而降低。迫切需要对研究这一现象的研究进行综述,因为它们应该为在非洲人群中使用的疫苗的设计和交付提供信息。