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      Elicitation of Robust Tier 2 Neutralizing Antibody Responses in Nonhuman Primates by HIV Envelope Trimer Immunization Using Optimized Approaches

      research-article
      1 , 2 , 3 , 22 , 2 , 4 , 22 , 1 , 2 , 3 , 5 , 2 , 6 , 1 , 2 , 3 , 10 , 2 , 18 , 19 ,   6 , 2 , 4 , 2 , 3 , 8 , 2 , 9 , 1 , 2 , 3 , 2 , 4 , 1 , 2 , 3 , 2 , 6 , 1 , 2 , 3 , 20 , 2 , 4 , 21 , 2 , 3 , 8 , 2 , 9 , 1 , 2 , 3 , 1 , 2 , 3 , 11 , 2 , 10 , 11 , 1 , 2 , 15 , 15 , 2 , 18 , 19 , 2 , 3 , 8 , 16 , 2 , 10 , 12 , 13 , 14 , 7 , 11 , 1 , 2 , 3 , 12 , 2 , 3 , 8 , 1 , 2 , 3 , 2 , 6 , 12 , 2 , 4 , 17 , , 1 , 2 , 3 , 12 , 23 , ∗∗
      Immunity
      Cell Press
      HIV vaccine, nonhuman primates, rhesus macaques, BG505, SOSIP, NFL, GC B cells, protein design, Tfh cells, germinal centers

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          Summary

          The development of stabilized recombinant HIV envelope trimers that mimic the virion surface molecule has increased enthusiasm for a neutralizing antibody (nAb)-based HIV vaccine. However, there is limited experience with recombinant trimers as immunogens in nonhuman primates, which are typically used as a model for humans. Here, we tested multiple immunogens and immunization strategies head-to-head to determine their impact on the quantity, quality, and kinetics of autologous tier 2 nAb development. A bilateral, adjuvanted, subcutaneous immunization protocol induced reproducible tier 2 nAb responses after only two immunizations 8 weeks apart, and these were further enhanced by a third immunization with BG505 SOSIP trimer. We identified immunogens that minimized non-neutralizing V3 responses and demonstrated that continuous immunogen delivery could enhance nAb responses. nAb responses were strongly associated with germinal center reactions, as assessed by lymph node fine needle aspiration. This study provides a framework for preclinical and clinical vaccine studies targeting nAb elicitation.

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          Highlights

          • Immunization protocols for rapid and consistent generation of autologous tier 2 nAbs

          • Germinal center responses predict and correlate with HIV nAbs after immunization

          • Env protein design curtails responses to the non-neutralizing V3-loop epitope

          • Subcutaneous and extended immunogen delivery enhances nAb generation

          Abstract

          There is limited experience with recombinant Env trimer immunogens in nonhuman primates. Pauthner et al. compare multiple Env trimer designs and immunization strategies for generating HIV neutralizing antibodies. They identify protocols for rapid and consistent generation of tier 2 nAbs, providing a framework for future pre-clinical and clinical vaccine studies.

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          Most cited references41

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          Sex differences in immune responses

          Males and females differ in their immunological responses to foreign and self-antigens and show distinctions in innate and adaptive immune responses. Certain immunological sex differences are present throughout life, whereas others are only apparent after puberty and before reproductive senescence, suggesting that both genes and hormones are involved. Furthermore, early environmental exposures influence the microbiome and have sex-dependent effects on immune function. Importantly, these sex-based immunological differences contribute to variations in the incidence of autoimmune diseases and malignancies, susceptibility to infectious diseases and responses to vaccines in males and females. Here, we discuss these differences and emphasize that sex is a biological variable that should be considered in immunological studies.
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            T follicular helper cell differentiation, function, and roles in disease.

            Follicular helper T (Tfh) cells are specialized providers of T cell help to B cells, and are essential for germinal center formation, affinity maturation, and the development of most high-affinity antibodies and memory B cells. Tfh cell differentiation is a multistage, multifactorial process involving B cell lymphoma 6 (Bcl6) and other transcription factors. This article reviews understanding of Tfh cell biology, including their differentiation, migration, transcriptional regulation, and B cell help functions. Tfh cells are critical components of many protective immune responses against pathogens. As such, there is strong interest in harnessing Tfh cells to improve vaccination strategies. Tfh cells also have roles in a range of other diseases, particularly autoimmune diseases. Overall, there have been dramatic advances in this young field, but there is much to be learned about Tfh cell biology in the interest of applying that knowledge to biomedical needs.
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              Germinal centers.

              Germinal centers (GCs) were described more than 125 years ago as compartments within secondary lymphoid organs that contained mitotic cells. Since then, it has become clear that this structure is the site of B cell clonal expansion, somatic hypermutation, and affinity-based selection, the combination of which results in the production of high-affinity antibodies. Decades of anatomical and functional studies have led to an overall model of how the GC reaction and affinity-based selection operate. More recently, the introduction of intravital imaging into the GC field has opened the door to direct investigation of certain key dynamic features of this microanatomic structure, sparking renewed interest in the relationship between cell movement and affinity maturation. We review these and other recent advances in our understanding of GCs, focusing on cellular dynamics and on the mechanism of selection of high-affinity B cells.
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                Author and article information

                Contributors
                Journal
                Immunity
                Immunity
                Immunity
                Cell Press
                1074-7613
                1097-4180
                20 June 2017
                20 June 2017
                : 46
                : 6
                : 1073-1088.e6
                Affiliations
                [1 ]Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037, USA
                [2 ]Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery, The Scripps Research Institute, La Jolla, CA 92037, USA
                [3 ]IAVI Neutralizing Antibody Center and the Collaboration for AIDS Vaccine Discovery, The Scripps Research Institute, La Jolla, CA 92037, USA
                [4 ]Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA
                [5 ]International AIDS Vaccine Initiative, New York, NY 10004, USA
                [6 ]Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA
                [7 ]Department of Microbiology and Immunology, Weill Medical College of Cornell University, New York, NY 10065, USA
                [8 ]Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, USA
                [9 ]Bioinformatics Core, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA
                [10 ]Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
                [11 ]Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, 1105 AZ Amsterdam, the Netherlands
                [12 ]Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology, and Harvard University, Cambridge, MA 02139, USA
                [13 ]Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
                [14 ]Departments of Biological Engineering and Materials Science & Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
                [15 ]Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA
                [16 ]Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037, USA
                [17 ]Division of Infectious Diseases, Department of Medicine, University of California, San Diego, La Jolla, CA 92037, USA
                [18 ]Yerkes National Primate Research Center, Emory University, Atlanta, GA 30322, USA
                [19 ]Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322, USA
                [20 ]Division of Infection & Immunity, University College London, London WC1E 6BT, UK
                [21 ]University of California, San Diego, La Jolla, CA 92093, USA
                Author notes
                []Corresponding author shane@ 123456lji.org
                [∗∗ ]Corresponding author burton@ 123456scripps.edu
                [22]

                These authors contributed equally

                [23]

                Lead Contact

                Article
                S1074-7613(17)30223-6
                10.1016/j.immuni.2017.05.007
                5483234
                28636956
                f052282f-f8cf-4274-aae9-66c503f77acb
                © 2017 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 24 March 2017
                : 26 April 2017
                : 26 May 2017
                Categories
                Resource

                Immunology
                hiv vaccine,nonhuman primates,rhesus macaques,bg505,sosip,nfl,gc b cells,protein design,tfh cells,germinal centers

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