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. 2018 Jul 6;9:1488. doi: 10.3389/fmicb.2018.01488

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Copyright © 2018 Surawut, Panpetch, Makjaroen, Tangtanatakul, Thim-Uam, Wongphoom, Tumwasorn and Leelahavanichkul.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Spleen weight (n = 5/group) (A) and the quantitative flow-cytometric analysis of splenocytes from wild-type (FcγRIIb +/+) and FcγRIIb-/- mice with phosphate buffer solution (PBS) gavage or H. pylori administration in the spleen plasma cell (CD138 +) (B), spleen activated B cell (CD19 + and CD80 +) (C), spleen germinal center B cell (CD19 + GC +) (D), spleen follicular B cell (CXCR5 + and B220 +) (E), spleen follicular helper T cell (CD3 + and CD4 + and CXCR5 +) (F) and spleen macrophage (F4/80 +) (G) were demonstrated. (n = 5–8/group); ^∗p < 0.05