Human CD27+ memory B cells colonize a superficial follicular zone in the palatine tonsils with similarities to the spleen. A multicolor immunofluorescence study of lymphoid tissue

• Published in: PloS one 2020-03, Vol.15 (3), p.e0229778-e0229778
• Main Authors: Lettau, Marie, Wiedemann, Annika, Schrezenmeier, Eva Vanessa, Giesecke-Thiel, Claudia, Dörner, Thomas
• Format: Article
• Language: English
• Subjects: Analogies; Antibodies; Antigens; Autoimmunity; B cells; Biology and Life Sciences; CD20 antigen; CD27 antigen; Characterization; Confocal microscopy; Epithelium; Fluorescence; Fluorescent antibody technique; Follicles; Germinal centers; Haptens; Humoral immunity; Identification; Immunofluorescence; Immunoglobulin A; Immunoglobulin D; Immunoglobulin G; Immunoglobulin M; Immunoglobulins; Immunological memory; Immunology; Localization; Lymphatic system; Lymphocytes; Lymphocytes B; Lymphocytes T; Lymphoid tissue; Medicine; Medicine and Health Sciences; Memory cells; Microscopy; Plasma cells; Research and Analysis Methods; Rheumatism; Rheumatology; Rodents; Scanning microscopy; Spleen; Studies; T cells; Time; Tonsil; Vaccination
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0229778

Memory B cell (mBC) induction and maintenance is one of the keys to long-term protective humoral immunity. MBCs are fundamental to successful medical interventions such as vaccinations and therapy in autoimmunity. However, their lifestyle and anatomic residence remain enigmatic in humans. Extrapolation from animal studies serves as a conceptual basis but might be misleading due to major anatomical distinctions between species. Multicolor immunofluorescence stainings on fixed and unfixed frozen tissue sections were established using primary antibodies coupled to haptens and secondary signal amplification. The simultaneous detection of five different fluorescence signals enabled the localization and characterization of human CD27+CD20+Ki67- mBCs for the first time within one section using laser scanning microscopy. As a result, human tonsillar mBCs were initially identified within their complex microenvironment and their relative location to naïve B cells, plasma cells and T cells could be directly studied and compared to the human splenic mBC niche. In all investigated tonsils (n = 15), mBCs appeared to be not only located in a so far subepithelial defined area but were also follicle associated with a previous undescribed gradual decline towards the follicular mantle comparable to human spleen. However, mBC areas around secondary follicles with large germinal centers (GCs) in tonsils showed interruptions and a general widening towards the epithelium while in spleen the mBC-containing marginal zones (MZ) around smaller GCs were relatively broad and symmetrical. Considerably fewer IgM+IgD+/- pre-switch compared to IgA+ or IgG+ post-switch mBCs were detected in tonsils in contrast to spleen. This study extends existing insights into the anatomic residence of human mBCs showing structural similarities of the superficial follicular area in human spleen and tonsil. Our data support the debate of renaming the human splenic MZ to 'superficial zone' in order to be aware of the differences in rodents and, moreover, to consider this term equally for the human palatine tonsil.