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We analysed the location, phenotype, and proliferation of GC PCs by immunohistology comparing them to PCs in the other two locations. Most PCs in GCs were strongly positive for CD38, CD138, CD27, IRF4, and intracellular (ic) IgG. They often accumulated in the basal light zone, but could also be found scattered in the entire light zone. In addition, rows of PCs occurred at the surface of the GC bordering the mantle zone, i.e., in the outer zone, and at the surface of the dark zone. The latter cells were often continuous with PCs in the extrafollicular area. The vast majority of GC PCs were negative for Ki-67. Only a few Ki-67<jats:sup>+<\/jats:sup>plasmablasts, predominantly icIgG<jats:sup>+<\/jats:sup>or icIgM<jats:sup>+<\/jats:sup>, were found inside GCs. In certain GCs PCs accumulated around capillaries and the adjacent perikarya of follicular dendritic cells (FDCs). Newly formed PCs might migrate from the basal to the superficial part of the light zone and then back to the dark zone surface to leave the GC. This guarantees an even distribution of secreted Ig for exchange with immune complexes on FDCs. The surface of the dark zone may also be an exit site for Ki-67<jats:sup>+<\/jats:sup>CD30<jats:sup>+<\/jats:sup>B lymphoblasts, which seed perifollicular and extrafollicular sites. We speculate that these cells tend to downmodulate CD20 and activation-induced deaminase and further up-regulate CD30 when developing into pre-plasmablasts.<\/jats:p>","DOI":"10.1007\/s00418-020-01861-1","type":"journal-article","created":{"date-parts":[[2020,6,30]],"date-time":"2020-06-30T03:11:55Z","timestamp":1593486715000},"page":"55-75","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":19,"title":["Plasma cells, plasmablasts, and AID+\/CD30+ B lymphoblasts inside and outside germinal centres: details of the basal light zone and the outer zone in human palatine tonsils"],"prefix":"10.1007","volume":"154","author":[{"given":"Birte S.","family":"Steiniger","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Linda","family":"Raimer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Anja","family":"Ecke","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Boris A.","family":"Stuck","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yalcin","family":"Cetin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2020,3,14]]},"reference":[{"key":"1861_CR1","doi-asserted-by":"crossref","first-page":"1169","DOI":"10.1084\/jem.187.8.1169","volume":"8","author":"C Arpin","year":"1998","unstructured":"Arpin C, de Bouteiller O, Razanajaona D, Fugier-Vivier I, Bri\u00e8re F, Banchereau J et al (1998) The normal counterpart of IgD myeloma cells in germinal center displays extensively mutated IgVH gene, C\u00b5\u2013C\u03b4 switch, and \u03bb light chain expression. 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