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      An Outdated Notion of Antibody Specificity is One of the Major Detrimental Assumptions of the Structure-Based Reverse Vaccinology Paradigm, Which Prevented It from Helping to Develop an Effective HIV-1 Vaccine

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          Abstract

          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.

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          The Structure of Scientific Revolution

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            Rational HIV immunogen design to target specific germline B cell receptors.

            Vaccine development to induce broadly neutralizing antibodies (bNAbs) against HIV-1 is a global health priority. Potent VRC01-class bNAbs against the CD4 binding site of HIV gp120 have been isolated from HIV-1-infected individuals; however, such bNAbs have not been induced by vaccination. Wild-type gp120 proteins lack detectable affinity for predicted germline precursors of VRC01-class bNAbs, making them poor immunogens to prime a VRC01-class response. We employed computation-guided, in vitro screening to engineer a germline-targeting gp120 outer domain immunogen that binds to multiple VRC01-class bNAbs and germline precursors, and elucidated germline binding crystallographically. When multimerized on nanoparticles, this immunogen (eOD-GT6) activates germline and mature VRC01-class B cells. Thus, eOD-GT6 nanoparticles have promise as a vaccine prime. In principle, germline-targeting strategies could be applied to other epitopes and pathogens.
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              Rescuing US biomedical research from its systemic flaws.

              The long-held but erroneous assumption of never-ending rapid growth in biomedical science has created an unsustainable hypercompetitive system that is discouraging even the most outstanding prospective students from entering our profession--and making it difficult for seasoned investigators to produce their best work. This is a recipe for long-term decline, and the problems cannot be solved with simplistic approaches. Instead, it is time to confront the dangers at hand and rethink some fundamental features of the US biomedical research ecosystem.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/41286
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                18 November 2014
                2014
                : 5
                : 593
                Affiliations
                [1] 1CNRS, Biotechnologie des Interactions Moleculaires, IREBS, School of Biotechnology, ESBS, University of Strasbourg , Illkirch, France
                Author notes

                Edited by: Kendall A. Smith, Weill Medical College of Cornell University, USA

                Reviewed by: Gianfranco Pancino, Institut national de la santé et de la recherche médicale (INSERM), France; Frank Miedema, University Medical Centre Utrecht, Netherlands

                *Correspondence: Marc H. V. Van Regenmortel, Pole API, Boulv Sebastien Brant, BP 10413, Illkirch cedex, France e-mail: vanregen@ 123456unistra.fr
                Present address: Marc H. V. Van Regenmortel, CNRS, UMR7242 – Institut de Recherche de l’Ecole de Biotechnologie de Strasbourg (IREBS), Université de Strasbourg, Illkirch, France

                This article was submitted to HIV and AIDS, a section of the journal Frontiers in Immunology.

                Article
                10.3389/fimmu.2014.00593
                4235417
                25477882
                a7cc39de-b11a-4bfe-8a65-e8b0119359e2
                Copyright © 2014 Van Regenmortel.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 26 July 2014
                : 05 November 2014
                Page count
                Figures: 0, Tables: 0, Equations: 0, References: 108, Pages: 8, Words: 8195
                Categories
                Immunology
                Review Article

                Immunology
                structure-based reverse vaccinology,hiv-1 vaccines,antibody polyspecificity,paradigm,immunological explanations

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