Kessing Cari F, Spudich Serena, Valcour Victor, Cartwright Pearline, Chalermchai Thep, Fletcher James L K, Takata Hiroshi, Nichols Carmen, Josey Benjamin J, Slike Bonnie, Krebs Shelly J, Sailsuta Napapon, Lerdlum Sukalaya, Jagodzinski Linda, Tipsuk Somporn, Suttichom Duanghathai, Rattanamanee Somprartthana, Zetterberg Henrik, Hellmuth Joanna, Phanuphak Nittaya, Robb Merlin L, Michael Nelson L, Ananworanich Jintanat, Trautmann Lydie
*Vaccine and Gene Therapy Institute-Florida, Port St Lucie, FL; †Currently, Cari F. Kessing, Department of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL; Pearline Cartwright, Department of Epidemiology and Biostatistics, Case Western Reserve University School of Medicine, Cleveland, OH; Carmen Nichols and Benjamin J. Josey, Cell Therapies Institute, Nova Southeastern University, FL; ‡Yale University School of Medicine, New Haven, CT; §Memory and Aging Center, Department of Neurology, University of California, San Francisco, CA; ‖SEARCH, The Thai Red Cross AIDS Research Center, Bangkok, Thailand; ¶Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD; #U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD; **University of Hawaii, Honolulu, HI; ††Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand; ‡‡Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, the Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden; and §§University College London Institute of Neurology, Queen Square, London, United Kingdom.
J Acquir Immune Defic Syndr. 2017 May 1;75(1):108-117. doi: 10.1097/QAI.0000000000001301.
Central nervous system (CNS) infiltration by CD8 T cells is associated with neuroinflammation in many neurodegenerative diseases, including HIV-associated dementia. However, the role of CD8 T cells in the CNS during acute HIV infection (AHI) is unknown.
We analyzed the phenotype, gene expression, T cell receptor (TCR) repertoire, and HIV specificity of CD8 T cells in cerebrospinal fluid (CSF) of a unique cohort captured during the earliest stages of AHI (n = 26), chronic (n = 23), and uninfected (n = 8).
CSF CD8 T cells were elevated in AHI compared with uninfected controls. The frequency of activated CSF CD8 T cells positively correlated to CSF HIV RNA and to markers of CNS inflammation. In contrast, activated CSF CD8 T cells during chronic HIV infection were associated with markers of neurological injury and microglial activation. CSF CD8 T cells in AHI exhibited increased functional gene expression profiles associated with CD8 T cells effector function, proliferation, and TCR signaling, a unique restricted TCR Vbeta repertoire and contained HIV-specific CD8 T cells directed to unique HIV epitopes compared with the periphery.
These results suggest that CSF CD8 T cells in AHI expanding in the CNS are functional and directed against HIV antigens. These cells could thus play a beneficial role protective of injury seen in chronic HIV infection if combination antiretroviral therapy is initiated early.
在包括人类免疫缺陷病毒相关痴呆症在内的许多神经退行性疾病中,中枢神经系统(CNS)中CD8 T细胞浸润与神经炎症相关。然而,急性人类免疫缺陷病毒感染(AHI)期间CD8 T细胞在中枢神经系统中的作用尚不清楚。
我们分析了在AHI最早阶段采集的一个独特队列(AHI组n = 26、慢性组n = 23、未感染组n = 8)脑脊液(CSF)中CD8 T细胞的表型、基因表达、T细胞受体(TCR)库和HIV特异性。
与未感染对照组相比,AHI患者的脑脊液CD8 T细胞升高。活化的脑脊液CD8 T细胞频率与脑脊液HIV RNA及中枢神经系统炎症标志物呈正相关。相比之下,慢性HIV感染期间活化的脑脊液CD8 T细胞与神经损伤和小胶质细胞活化标志物相关。与外周血相比,AHI患者脑脊液CD8 T细胞表现出与CD8 T细胞效应功能、增殖和TCR信号传导相关的功能基因表达谱增加,TCR Vβ库独特受限,且含有针对独特HIV表位的HIV特异性CD8 T细胞。
这些结果表明,在中枢神经系统中扩增的AHI患者脑脊液CD8 T细胞具有功能且针对HIV抗原。因此,如果早期启动联合抗逆转录病毒治疗,这些细胞可能在保护慢性HIV感染中所见损伤方面发挥有益作用。