6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Generation of High Quality Memory B Cells

      review-article

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Protection against pathogen re-infection is mediated, in large part, by two humoral cellular compartments, namely, long-lived plasma cells and memory B cells. Recent data have reinforced the importance of memory B cells, particularly in response to re-infection of different viral subtypes or in response with viral escape mutants. In regard to memory B cell generation, considerable advancements have been made in recent years in elucidating its basic mechanism, which seems to well explain why the memory B cells pool can deal with variant viruses. Despite such progress, efforts to develop vaccines that induce broadly protective memory B cells to fight against rapidly mutating pathogens such as influenza virus and HIV have not yet been successful. Here, we discuss recent advances regarding the key signals and factors regulating germinal center-derived memory B cell development and activation and highlight the challenges for successful vaccine development.

          Related collections

          Most cited references75

          • Record: found
          • Abstract: found
          • Article: not found

          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.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            B Cell Responses: Cell Interaction Dynamics and Decisions

            B cells and the antibodies they produce have a deeply penetrating influence on human physiology. Here we review current understanding of how B cell responses are initiated, the different paths to generate short- and long-lived plasma cells, germinal center cells, and memory cells, and how each path impacts antibody diversity, selectivity and affinity. We discuss how basic research is informing efforts to generate vaccines that induce broadly neutralizing antibodies against viral pathogens, revealing the special features associated with allergen-reactive IgE responses, and uncovering the antibody-independent mechanisms by which B cells contribute to health and disease.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Germinal Center B Cell Dynamics.

              Germinal centers (GCs) are the site of antibody diversification and affinity maturation and as such are vitally important for humoral immunity. The study of GC biology has undergone a renaissance in the past 10 years, with a succession of findings that have transformed our understanding of the cellular dynamics of affinity maturation. In this review, we discuss recent developments in the field, with special emphasis on how GC cellular and clonal dynamics shape antibody affinity and diversity during the immune response.
                Bookmark

                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                12 January 2022
                2021
                : 12
                : 825813
                Affiliations
                [1] 1Laboratory of Lymphocyte Differentiation, WPI Immunology Frontier Research Center, Osaka University , Osaka, Japan
                [2] 2Center for Infectious Diseases Education and Research, Osaka University , Osaka, Japan
                [3] 3Laboratory for Lymphocyte Differentiation, RIKEN Center for Integrative Medical Sciences , Kanagawa, Japan
                Author notes

                Edited by: Jieun Oh, Korea Advanced Institute of Science and Technology, South Korea

                Reviewed by: Kim Good-Jacobson, Monash University, Australia; Masato Kubo, Tokyo University of Science, Japan

                *Correspondence: Takeshi Inoue, inoue@ 123456ifrec.osaka-u.ac.jp ; Tomohiro Kurosaki, kurosaki@ 123456ifrec.osaka-u.ac.jp

                This article was submitted to Immunological Memory, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2021.825813
                8790150
                d29734fa-5d47-460a-88d4-e6570f8bb62e
                Copyright © 2022 Inoue, Shinnakasu and Kurosaki

                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) and the copyright owner(s) 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
                : 30 November 2021
                : 23 December 2021
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 75, Pages: 10, Words: 5890
                Funding
                Funded by: Japan Society for the Promotion of Science , doi 10.13039/501100001691;
                Award ID: JP21H02749, JP21H02740, JP19H01028
                Funded by: Takeda Science Foundation , doi 10.13039/100007449;
                Funded by: Naito Foundation , doi 10.13039/100007428;
                Funded by: Sumitomo Foundation , doi 10.13039/100008608;
                Categories
                Immunology
                Review

                Immunology
                memory b cell,germinal center,vaccine,broadly neutralizing antibody,bcr affinity
                Immunology
                memory b cell, germinal center, vaccine, broadly neutralizing antibody, bcr affinity

                Comments

                Comment on this article