Stoll-Keller Françoise, Barth Heidi, Fafi-Kremer Samira, Zeisel Mirjam B, Baumert Thomas F
Inserm, U748 et Laboratoire de Virologie des Hôpitaux Universitaires de Strasbourg, 3 rue Koeberlé 67000 Strasbourg, France.
Expert Rev Vaccines. 2009 Mar;8(3):333-45. doi: 10.1586/14760584.8.3.333.
Development of an effective vaccine against the hepatitis C virus (HCV) has long been defined as a difficult challenge due to the considerable variability of this RNA virus and the observation that convalescent humans and chimpanzees could be re-infected after re-exposure. On the other hand, progress in the understanding of antiviral immune responses in patients with viral clearance has elucidated key mechanisms playing a role in the control of viral infection. Studies investigating prophylactic vaccine approaches in chimpanzees have confirmed that the induction and maintenance of strong helper and cytotoxic T-cell immune responses against multiple viral epitopes is necessary for protection against viral clearance and chronic infection. A multispecific B-cell response, resulting in rapid induction of cross-neutralizing antibodies may assist cellular responses. Therapeutic vaccine formulations currently being evaluated in clinical trials are facing the fact that the immune system of chronic carriers is impaired and needs the restoration of T-cell functions to enhance their efficacy.
长期以来,开发一种有效的抗丙型肝炎病毒(HCV)疫苗一直被视为一项艰巨的挑战,原因在于这种RNA病毒具有相当大的变异性,而且有观察表明,康复的人类和黑猩猩在再次接触病毒后可能会再次感染。另一方面,对病毒清除患者抗病毒免疫反应的理解取得的进展,阐明了在控制病毒感染中起作用的关键机制。在黑猩猩身上研究预防性疫苗方法的研究证实,针对多个病毒表位诱导并维持强大的辅助性和细胞毒性T细胞免疫反应,对于预防病毒清除和慢性感染是必要的。多特异性B细胞反应导致快速诱导交叉中和抗体,可能有助于细胞反应。目前正在临床试验中评估的治疗性疫苗制剂面临着这样一个事实,即慢性携带者的免疫系统受损,需要恢复T细胞功能以提高其疗效。