Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham.
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
J Infect Dis. 2019 Oct 8;220(10):1620-1628. doi: 10.1093/infdis/jiz368.
HLA-I-associated human immunodeficiency virus (HIV) adaptation is known to negatively affect disease progression and CD8 T-cell responses. We aimed to assess how HLA-I-associated adaptation affects HIV vaccine-induced CD8 T-cell responses in 2 past vaccine efficacy trials. We found that vaccine-encoded adapted epitopes were less immunogenic than vaccine-encoded nonadapted epitopes, and adapted epitope-specific responses were less polyfunctional than nonadapted epitope-specific responses. Along those lines, vaccine recipients with higher HLA-I adaptation to the Gag vaccine insert mounted less polyfunctional CD8 T-cell responses at the protein level. Breadth of response, which correlated with viral control in recipients who became infected, is also dampened by HLA-I adaptation. These findings suggest that HLA-I-associated adaptation is an important consideration for strategies aiming to induce robust CD8 T-cell responses.
HLA-I 相关的人类免疫缺陷病毒 (HIV) 适应性已被证实会对疾病进展和 CD8 T 细胞反应产生负面影响。我们旨在评估 HLA-I 相关适应性如何影响过去两项疫苗功效试验中 HIV 疫苗诱导的 CD8 T 细胞反应。我们发现,疫苗编码的适应性表位比疫苗编码的非适应性表位的免疫原性更低,而适应性表位特异性反应比非适应性表位特异性反应的多功能性更低。沿着这些思路,对 Gag 疫苗插入物具有更高 HLA-I 适应性的疫苗接种者在蛋白质水平上表现出较少的多功能 CD8 T 细胞反应。反应的广度与受感染的受者的病毒控制相关,也因 HLA-I 适应性而减弱。这些发现表明,HLA-I 相关的适应性是旨在诱导强大的 CD8 T 细胞反应的策略的一个重要考虑因素。