Logo Logo
Hilfe
Hilfe
Switch Language to English

Zhang, Yang; Garcia-Ibanez, Laura; Ulbricht, Carolin; Lok, Laurence S. C.; Pike, Jeremy A.; Mueller-Winkler, Jennifer; Dennison, Thomas W.; Ferdinand, John R.; Burnett, Cameron J. M.; Yam-Puc, Juan C.; Zhang, Lingling; Alfaro, Raul Maqueda; Takahama, Yousuke; Ohigashi, Izumi; Brown, Geoffrey; Kurosaki, Tomohiro; Tybulewicz, Victor L. J.; Rot, Antal; Hauser, Anja E.; Clatworthy, Menna R. und Toellner, Kai-Michael (2022): Recycling of memory B cells between germinal center and lymph node subcapsular sinus supports affinity maturation to antigenic drift. In: Nature Communications, Bd. 13, Nr. 1, 2460

Volltext auf 'Open Access LMU' nicht verfügbar.

Abstract

Infection or vaccination leads to the development of germinal centers (GC) where B cells evolve high affinity antigen receptors, eventually producing antibody-forming plasma cells or memory B cells. Here we follow the migratory pathways of B cells emerging from germinal centers (B-EM) and find that many B-EM cells migrate into the lymph node subcapsular sinus (SCS) guided by sphingosine-1-phosphate (S1P). From the SCS, B-EM cells may exit the lymph node to enter distant tissues, while some B-EM cells interact with and take up antigen from SCS macrophages, followed by CCL21-guided return towards the GC. Disruption of local CCL21 gradients inhibits the recycling of B-EM cells and results in less efficient adaption to antigenic variation. Our findings thus suggest that the recycling of antigen variant-specific B-EM cells and transport of antigen back to GC may support affinity maturation to antigenic drift. Activated B cell enter germinal centers (GC) to become plasma cells and memory B cells. Here the authors show that some memory B cells recycle to GC via CCL-21 mediated chemotaxis to deliver antigens from the lymph node subcapsular sinus (SCS) to potentially contribute to affinity maturation and antigenic drift.

Dokument bearbeiten Dokument bearbeiten