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IL-17–producing follicular Th cells enhance plasma cell differentiation in lupus-prone mice
Vera Kim, Kyungwoo Lee, Hong Tian, Su Hwa Jang, Betty Diamond, Sun Jung Kim
Vera Kim, Kyungwoo Lee, Hong Tian, Su Hwa Jang, Betty Diamond, Sun Jung Kim
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Research Article Immunology

IL-17–producing follicular Th cells enhance plasma cell differentiation in lupus-prone mice

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Abstract

Follicular Th (Tfh) cells are key CD4+ Th cells involved in regulating B cell differentiation in the germinal center. Mice with conditional KO (CKO) of B lymphocyte-induced maturation protein-1 (BLIMP-1) expression in CD11chi DCs (Prdm1 CKO) spontaneously develop a lupus-like disease. We found an increase in the number of Tfh cells in secondary lymphoid organs in lupus-prone Prdm1-CKO mice. B cells stimulated with Tfh cells become Ab-secreting cells (ASCs); there was an increase in ASC differentiation mediated by Tfh cells from Prdm1-CKO mice compared with Tfh cells from control mice. This was mainly due to the increased expression of molecules within the IL-23/IL-17 pathway in Tfh cells from Prdm1-CKO mice. There was an increased frequency of IL-17A+ Tfh cells in Prdm1-CKO mice. These Tfh cells secrete IL-17A and an increased amount of IL-21. Furthermore, neutralizing IL-17A and IL-21 reduced ASC differentiation induced by Tfh cells. Lastly, we found the expression of IL-1β and IL-6 was increased in BLIMP-1–deficient DCs, which are key for Th17 induction. Altogether, the lack of BLIMP-1 expression in DCs induces not only an increased number of Tfh cells, but also functionally distinct Tfh cells that lead to increased ASC differentiation.

Authors

Vera Kim, Kyungwoo Lee, Hong Tian, Su Hwa Jang, Betty Diamond, Sun Jung Kim

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Figure 3

RNA-seq reveals an increased IL-17 pathway in Tfh cells from Prdm1-CKO mice.

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RNA-seq reveals an increased IL-17 pathway in Tfh cells from Prdm1-CKO m...
NP-CGG–immunized Prdm1-CKO and CTL mice were sacrificed at day 7 after immunization and transcriptome analysis were done by RNA-seq. (A) A volcano plot of differentially expressed genes was plotted. Positive fold change means gene expression is higher in Prdm1-CKO mice than control mice. To confirm the result in A, a separate cohort of mice was immunized and differential expression of genes in Tfh cells was measured by qPCR (B) (n = 6 for both CTL and KO). Protein expression of BAFF-R and IL-23R in CD4+ T cell subsets was measured by flow cytometry (C) (n = 11 for CTL and n = 8 for KO). A representative flow image of staining is on the top. Each dot represents an individual mouse, and the bar graph indicates the mean from 3 independent experiments. An unpaired 2-tailed Student’s t test (Mann-Whitney) was used.

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