Shapiro Stuart Z
Vaccine Research Program, Division of AIDS, National Institute of Allergy and Infectious Diseases , Bethesda, Maryland.
AIDS Res Hum Retroviruses. 2014 Apr;30(4):325-9. doi: 10.1089/AID.2013.0114. Epub 2013 Nov 22.
Realization of individual and public health benefit from an HIV vaccine requires clinical testing to demonstrate efficacy. To facilitate clinical testing, preclinical HIV vaccine developers should consider the realities of clinical practice and the conduct of clinical trials in product design. There are several essentially different approaches to prophylactic HIV vaccine design: (1) induce immunity that allows infection but reduces initial peak viremia and viral load set point; (2) induce immunity that allows infection but controls viremia to below the level of detection; (3) induce immunity that allows infection but promotes viral clearance before disease (classic vaccine approach); (4) induce "sterilizing immunity" that prevents acquisition of infection. Each approach presents different challenges for clinical product development. Current clinical trial practices and evolving treatment standards may make it infeasible to perform an efficacy trial of a preventive vaccine that only modestly reduces viremia. A vaccine that promotes control of viremia to below the level of detection is testable but will require extended follow-up to determine how long virus control persists; once control is lost boosting with the same vaccine may not be useful. A vaccine that permits infection but promotes subsequent complete clearance of the virus from the body will require the development and validation of an effective assay for virus clearance. A vaccine that prevents acquisition of infection is the most straightforward to test in the clinic, but escalating costs require more attention by vaccine developers to understanding how the vaccine works and the breadth of protection. All types of vaccine require attention to effect size to ensure adequate powering of efficacy trials.
实现艾滋病毒疫苗对个人和公共健康的益处需要进行临床试验以证明其有效性。为便于开展临床试验,临床前艾滋病毒疫苗研发人员在产品设计时应考虑临床实践的实际情况以及临床试验的实施。预防性艾滋病毒疫苗设计有几种本质上不同的方法:(1)诱导产生的免疫力可允许感染,但能降低初始峰值病毒血症和病毒载量设定点;(2)诱导产生的免疫力可允许感染,但能将病毒血症控制在检测水平以下;(3)诱导产生的免疫力可允许感染,但能在疾病发生前促进病毒清除(经典疫苗方法);(4)诱导产生“无菌免疫力”以防止感染。每种方法在临床产品开发中都面临不同的挑战。当前的临床试验实践和不断发展的治疗标准可能使仅适度降低病毒血症的预防性疫苗进行疗效试验变得不可行。一种能将病毒血症控制在检测水平以下的疫苗是可测试的,但需要延长随访时间以确定病毒控制能持续多久;一旦失去控制,用同一种疫苗加强免疫可能无济于事。一种允许感染但能促进随后病毒从体内完全清除的疫苗将需要开发和验证有效的病毒清除检测方法。一种能防止感染的疫苗在临床上测试最为直接,但成本不断攀升要求疫苗研发人员更多地关注了解疫苗的作用方式和保护范围。所有类型的疫苗都需要关注效应大小,以确保疗效试验有足够的效力。