Literature DB >> 29500990

A synthetic stroma-free germinal center niche for efficient generation of humoral immunity ex vivo.

Kyung-Ho Roh1, Hannah W Song1, Pallab Pradhan1, Kevin Bai1, Caitlin D Bohannon2, Gordon Dale2, Jardin Leleux1, Joshy Jacob2, Krishnendu Roy3.   

Abstract

B cells play a major role in the adaptive immune response by producing antigen-specific antibodies against pathogens and imparting immunological memory. Following infection or vaccination, antibody-secreting B cells and memory B cells are generated in specialized regions of lymph nodes and spleens, called germinal centers. Here, we report a fully synthetic ex-vivo system that recapitulates the generation of antigen-specific germinal-center (GC) like B cells using material-surface driven polyvalent signaling. This synthetic germinal center (sGC) reaction was effectively induced using biomaterial-based artificial "follicular T helper cells (TFH)" that provided both natural CD40-CD40L ligation as well as crosslinking of CD40 and by mimicking artificial "follicular dendritic cells (FDC)" to provide efficient, polyvalent antigen presentation. The artificial sGC reaction resulted in efficient B cell expansion, immunoglobulin (Ig) class switching, and expression of germinal center phenotypes. Antigen presentation during sGC reaction selectively enhanced the antigen-specific B cell population and induced somatic hyper-mutations for potential affinity maturation. The resulting B cell population consisted primarily of GC-like B cells (centrocytes) as well as some plasma-like B cells expressing CD138. With concurrent cell sorting, we successfully created highly enriched populations of antigen-specific B cells. Adoptive transfer of these GC-like B cells into non-irradiated isogeneic or non-lethally irradiated congenic recipient mice showed successful engraftment and survival of the donor cells for the 4 week test period. We show that this material-surface driven sGC reaction can be successfully applied to not only splenic B cells but also B cells isolated from more therapeutically relevant sources such as peripheral blood mononuclear cells (PBMCs), thus making our current work an exciting prospect in the new era of personalized medicine and custom-immunotherapy.
Copyright © 2018 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Antigen specificity; B cell; CD40L; Somatic hypermutation; Synthetic germinal center

Mesh:

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Year:  2018        PMID: 29500990     DOI: 10.1016/j.biomaterials.2018.02.039

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  4 in total

1.  Lipid Membrane-Based Antigen Presentation to B Cells Using a Fully Synthetic Ex Vivo Germinal Center Model.

Authors:  Liana Kramer; Hannah W Song; Kaiya Mitchell; Mythili Kartik; Ritika Jain; Victoria Lozano Escarra; Enrique Quiros; Harrison Fu; Ankur Singh; Krishnendu Roy
Journal:  Adv Nanobiomed Res       Date:  2022-04-28

Review 2.  In Vitro and In Vivo Models of CLL-T Cell Interactions: Implications for Drug Testing.

Authors:  Eva Hoferkova; Sona Kadakova; Marek Mraz
Journal:  Cancers (Basel)       Date:  2022-06-23       Impact factor: 6.575

3.  Multiscale engineering of immune cells and lymphoid organs.

Authors:  Sungwoong Kim; Shivem B Shah; Pamela L Graney; Ankur Singh
Journal:  Nat Rev Mater       Date:  2019-04-03       Impact factor: 66.308

4.  Complex human adenoid tissue-based ex vivo culture systems reveal anti-inflammatory drug effects on germinal center T and B cells.

Authors:  Angelika Schmidt; Johanna E Huber; Özen Sercan Alp; Robert Gürkov; Christoph A Reichel; Matthias Herrmann; Oliver T Keppler; Thomas Leeuw; Dirk Baumjohann
Journal:  EBioMedicine       Date:  2020-02-27       Impact factor: 8.143

  4 in total

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