AIMS: Extrafollicular activation of B cells is rarely observed in human lymph nodes. The aim of this study was to extensively analyse the expression of surface molecules and transcription factors in four such cases, comparing them with follicular B cells and medullary cord plasma cells. METHODS AND RESULTS: Various combinations of B-cell-related surface markers and transcription factors were studied by triple immunofluorescence. While in the germinal centre, reactive immunoglobulin production occurred exclusively in non-proliferating cells, in extrafollicular activation proliferation of B cells and immunoglobulin production coexisted. In two of these cases proliferating cells were mainly IgG+CD27+, i.e. derived from class-switched postgerminal centre memory B cells. Some of these cells expressed CD30. In the other two cases, immunoglobulin-forming cells were non-class-switched IgM+CD27- B cells, representing a primary expansion of naive B cells. CONCLUSIONS: Extrafollicular B-cell activation is the morphological correlate of rapid B-cell responses that do not involve the germinal centres. It is pathogenetically heterogeneous, comprising primary responses that occur prior to, or independent of, germinal centre reaction or memory cell activation in recall responses.
AIMS: Extrafollicular activation of B cells is rarely observed in human lymph nodes. The aim of this study was to extensively analyse the expression of surface molecules and transcription factors in four such cases, comparing them with follicular B cells and medullary cord plasma cells. METHODS AND RESULTS: Various combinations of B-cell-related surface markers and transcription factors were studied by triple immunofluorescence. While in the germinal centre, reactive immunoglobulin production occurred exclusively in non-proliferating cells, in extrafollicular activation proliferation of B cells and immunoglobulin production coexisted. In two of these cases proliferating cells were mainly IgG+CD27+, i.e. derived from class-switched postgerminal centre memory B cells. Some of these cells expressed CD30. In the other two cases, immunoglobulin-forming cells were non-class-switched IgM+CD27- B cells, representing a primary expansion of naive B cells. CONCLUSIONS: Extrafollicular B-cell activation is the morphological correlate of rapid B-cell responses that do not involve the germinal centres. It is pathogenetically heterogeneous, comprising primary responses that occur prior to, or independent of, germinal centre reaction or memory cell activation in recall responses.
Authors: Laura S Treml; William J Quinn; John F Treml; Jean L Scholz; Michael P Cancro Journal: Arch Immunol Ther Exp (Warsz) Date: 2008-05-30 Impact factor: 4.291
Authors: Jasmin D Haslbauer; Carl Zinner; Anna K Stalder; Jan Schneeberger; Thomas Menter; Stefano Bassetti; Kirsten D Mertz; Philip Went; Matthias S Matter; Alexandar Tzankov Journal: Front Immunol Date: 2021-12-13 Impact factor: 7.561
Authors: Danny Jonigk; Christopher Werlein; Saskia von Stillfried; Peter Boor; Till Acker; Martin Aepfelbacher; Kerstin U Amann; Gustavo Baretton; Peter Barth; Rainer M Bohle; Andreas Büttner; Reinhard Büttner; Reinhard Dettmeyer; Philip Eichhorn; Sefer Elezkurtaj; Irene Esposito; Katja Evert; Matthias Evert; Falko Fend; Nikolaus Gaßler; Stefan Gattenlöhner; Markus Glatzel; Heike Göbel; Elise Gradhand; Torsten Hansen; Arndt Hartmann; Axel Heinemann; Frank L Heppner; Julia Hilsenbeck; David Horst; Jan C Kamp; Gita Mall; Bruno Märkl; Benjamin Ondruschka; Jessica Pablik; Susanne Pfefferle; Alexander Quaas; Helena Radbruch; Christoph Röcken; Andreas Rosenwald; Wilfried Roth; Martina Rudelius; Peter Schirmacher; Julia Slotta-Huspenina; Kevin Smith; Linna Sommer; Konrad Stock; Philipp Ströbel; Stephanie Strobl; Ulf Titze; Gregor Weirich; Joachim Weis; Martin Werner; Claudia Wickenhauser; Thorsten Wiech; Peter Wild; Tobias Welte Journal: Virchows Arch Date: 2022-04-01 Impact factor: 4.535