Nicolas Quizon

ORCID: 0000-0002-8038-5988
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About
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Research Areas
  • Monoclonal and Polyclonal Antibodies Research
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology

National Institute of Allergy and Infectious Diseases
2018

National Institutes of Health
2018

Protective antibody responses to vaccination or infection depend on affinity maturation, a process by which high-affinity germinal center (GC) B cells are selected the basis of their ability bind, gather, and present antigen T follicular helper (Tfh) cells. Here, we show that human GC have intrinsically higher-affinity thresholds for both cell receptor (BCR) signaling gathering as compared with naïve these functions mediated distinct cellular structures pathways ultimately lead affinity- Tfh...

10.1126/sciimmunol.aau6598 article EN Science Immunology 2018-11-30

Abstract The selection of GC B cells that express high affinity cell receptors (BCRs) is driven by the ability to both signal through BCR and extract antigen present it follicular helper T (T FH cells). Using anti-kappa antibodies low (KD=3.9×10 −7 ) versus (KD=2.4×10 −9 affinities attached membranes as surrogate antigens, we show LZ are able discriminate between these responded only antigen. In contrast, naïve antigens. engaged membrane associated antigens highly dynamic F-actin ezrin-rich...

10.4049/jimmunol.200.supp.107.17 article EN The Journal of Immunology 2018-05-01
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