Van Regenmortel Marc H V
CNRS, Biotechnologie des Interactions Moleculaires, IREBS, School of Biotechnology, ESBS, University of Strasbourg , Illkirch , France.
Front Immunol. 2014 Nov 18;5:593. doi: 10.3389/fimmu.2014.00593. eCollection 2014.
The importance of paradigms for guiding scientific research is explained with reference to the seminal work of Karl Popper and Thomas Kuhn. A prevalent paradigm, followed for more than a decade in HIV-1 vaccine research, which gave rise to the strategy known as structure-based reverse vaccinology is described in detail. Several reasons why this paradigm did not allow the development of an effective HIV-1 vaccine are analyzed. A major reason is the belief shared by many vaccinologists that antibodies possess a narrow specificity for a single epitope and are not polyspecific for a diverse group of potential epitopes. When this belief is abandoned, it becomes obvious that the one particular epitope structure observed during the crystallographic analysis of a neutralizing antibody-antigen complex does not necessarily reveal, which immunogenic structure should be used to elicit the same type of neutralizing antibody. In the physical sciences, scientific explanations are usually presented as logical deductions derived from a relevant law of nature together with certain initial conditions. In immunology, causal explanations in terms of a single cause acting according to a law of nature are not possible because numerous factors always play a role in bringing about an effect. The implications of this state of affairs for the rational design of HIV vaccines are outlined. An alternative approach to obtain useful scientific understanding consists in intervening empirically in the immune system and it is suggested that manipulating the system experimentally is needed to learn to control it and achieve protective immunity by vaccination.
本文通过引用卡尔·波普尔(Karl Popper)和托马斯·库恩(Thomas Kuhn)的开创性著作,解释了范式对指导科学研究的重要性。详细描述了在HIV-1疫苗研究中流行了十多年的一种范式,该范式催生了所谓的基于结构的反向疫苗学策略。分析了该范式未能促成有效HIV-1疫苗研发的几个原因。一个主要原因是许多疫苗学家所持的观点,即抗体对单个表位具有狭窄的特异性,而非对多种潜在表位具有多特异性。当摒弃这一观点时,就会明显发现,在对中和抗体-抗原复合物进行晶体学分析时观察到的特定表位结构,不一定能揭示应使用哪种免疫原性结构来引发同类型的中和抗体。在物理科学中,科学解释通常呈现为从相关自然法则以及某些初始条件推导出来的逻辑演绎。在免疫学中,不可能依据自然法则由单一原因进行因果解释,因为在产生某种效应的过程中,总是有众多因素在起作用。概述了这种情况对HIV疫苗合理设计的影响。获得有用科学认识的另一种方法是对免疫系统进行实证干预,并且有人提出需要通过实验操纵该系统,以便学会控制它并通过接种疫苗实现保护性免疫。