Lukacher Aron E
Department of Pathology, Woodruff Memorial Research Building, Rm. 7307, Emory University School of Medicine, 1639 Pierce Drive, Atlanta, GA 30322, USA.
Immunol Res. 2004;29(1-3):139-50. doi: 10.1385/IR:29:1-3:139.
Polyomaviruses establish persistent infection in a variety of hosts, including humans, where they pose an oncogenic threat under conditions of depressed immune function. Control of persistent infection by these DNA tumor viruses requires continuous immunosurveillance by functionally competent antiviral CD8+ T cells. Repetitive antigen encounter by these T cells, however, often leads to their deletion or inactivation. Elucidation of the in vivo mechanisms that sustain antigen-specific CD8+ T-cell effector activity in the face of persistent antigen is essential for devising immunotherapeutic strategies against viral oncogenesis.
多瘤病毒可在包括人类在内的多种宿主中建立持续感染,在免疫功能低下的情况下,它们会构成致癌威胁。这些DNA肿瘤病毒对持续感染的控制需要功能正常的抗病毒CD8 + T细胞进行持续的免疫监视。然而,这些T细胞反复接触抗原往往会导致它们的缺失或失活。阐明在持续存在抗原的情况下维持抗原特异性CD8 + T细胞效应活性的体内机制,对于设计针对病毒致癌作用的免疫治疗策略至关重要。