Clinical Cooperation Group, Pediatric Tumor Immunology, Helmholtz-Zentrum München, Marchioninistrasse 25, Munich, Germany.
Eur J Cell Biol. 2012 Jan;91(1):31-5. doi: 10.1016/j.ejcb.2011.01.007. Epub 2011 Apr 1.
Epstein-Barr virus (EBV) establishes lifelong persistent infections in humans and has been implicated in the pathogenesis of several human malignancies. Protective immunity against EBV is mediated by T cells, as indicated by an increased incidence of EBV-associated malignancies in immunocompromised patients, and by the successful treatment of EBV-associated post-transplant lymphoproliferative disease (PTLD) in transplant recipients by the infusion of polyclonal EBV-specific T cell lines. To implement this treatment modality as a conventional therapeutic option, and to extend this protocol to other EBV-associated diseases, generic and more direct approaches for the generation of EBV-specific T cell lines enriched in disease-relevant specificities need to be developed. To this aim, we studied the poorly defined EBV-specific CD4+ T cell response during acute and chronic infection.
EB 病毒(EBV)在人类中建立了终身持续性感染,并被认为与几种人类恶性肿瘤的发病机制有关。针对 EBV 的保护性免疫是由 T 细胞介导的,这表明免疫功能低下的患者 EBV 相关恶性肿瘤的发病率增加,以及通过输注多克隆 EBV 特异性 T 细胞系成功治疗移植受者的 EBV 相关移植后淋巴组织增生性疾病 (PTLD)。为了将这种治疗方式作为常规治疗选择实施,并将该方案扩展到其他 EBV 相关疾病,需要开发更通用和更直接的方法来产生富含疾病相关特异性的 EBV 特异性 T 细胞系。为此,我们研究了急性和慢性感染期间定义不明确的 EBV 特异性 CD4+ T 细胞反应。