Sagar Divya, Masih Shet, Schell Todd, Jacobson Steven, Comber Joseph D, Philip Ramila, Wigdahl Brian, Jain Pooja, Khan Zafar K
Department of Microbiology and Immunology, Drexel Institute for Biotechnology & Virology Research, Drexel University College of Medicine, Philadelphia, PA, USA.
Department of Microbiology and Immunology, The Pennsylvania State University College of Medicine, Hershey, PA, USA.
Vaccine. 2014 May 30;32(26):3274-84. doi: 10.1016/j.vaccine.2014.03.087. Epub 2014 Apr 13.
Viral oncoprotein Tax plays key roles in transformation of human T-cell leukemia virus (HTLV-1)-infected T cells leading to adult T-cell leukemia (ATL), and is the key antigen recognized during HTLV-associated myelopathy (HAM). In HLA-A2+ asymptomatic carriers as well as ATL and HAM patients, Tax(11-19) epitope exhibits immunodominance. Here, we evaluate CD8 T-cell immune response against this epitope in the presence and absence of dendritic cells (DCs) given the recent encouraging observations made with Phase 1 DC-based vaccine trial for ATL. To facilitate these studies, we first generated an HLA-A2/DTR hybrid mouse strain carrying the HLA-A2.1 and CD11c-DTR genes. We then studied CD8 T-cell immune response against Tax(11-19) epitope delivered in the absence or presence of Freund's adjuvant and/or DCs. Overall results demonstrate that naturally presented Tax epitope could initiate an antigen-specific CD8T cell response in vivo but failed to do so upon DC depletion. Presence of adjuvant potentiated Tax(11-19)-specific response. Elevated serum IL-6 levels coincided with depletion of DCs whereas decreased TGF-β was associated with adjuvant use. Thus, Tax(11-19) epitope is a potential candidate for the DC-based anti-HTLV-1 vaccine and the newly hybrid mouse strain could be used for investigating DC involvement in human class-I-restricted immune responses.
病毒癌蛋白Tax在人类T细胞白血病病毒1型(HTLV-1)感染的T细胞转化为成人T细胞白血病(ATL)过程中发挥关键作用,并且是在HTLV相关脊髓病(HAM)期间被识别的关键抗原。在HLA-A2+无症状携带者以及ATL和HAM患者中,Tax(11-19)表位表现出免疫优势。鉴于最近基于树突状细胞(DC)的ATL 1期疫苗试验取得了令人鼓舞的观察结果,我们在此评估在有或没有DC的情况下针对该表位的CD8 T细胞免疫反应。为便于开展这些研究,我们首先构建了一种携带HLA-A2.1和CD11c-DTR基因的HLA-A2/DTR杂交小鼠品系。然后,我们研究了在不存在或存在弗氏佐剂和/或DC的情况下针对Tax(11-19)表位的CD8 T细胞免疫反应。总体结果表明,天然呈递的Tax表位可在体内引发抗原特异性CD8 T细胞反应,但在DC耗竭后则无法引发。佐剂的存在增强了Tax(11-19)特异性反应。血清IL-6水平升高与DC耗竭同时出现,而TGF-β降低与佐剂的使用有关。因此,Tax(11-19)表位是基于DC的抗HTLV-1疫苗的潜在候选物,新的杂交小鼠品系可用于研究DC在人类I类限制性免疫反应中的作用。