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The therapeutic effect of anti-CD19 antibody on DHEA-induced PCOS mice

•aCD19 Ab improved ovarian pathological structure and function of PCOS mice.•aCD19 Ab reduced splenic MZB cells and serum IgM level of PCOS mice.•aCD19 Ab reduced macrophage infiltration and TNF-α expression in ovaries of PCOS mice.•TNF-α promoted granulosa cell apoptosis. Immune dysregulation has b...

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Published in:International immunopharmacology 2024-03, Vol.130, p.111711-111711, Article 111711
Main Authors: Wang, Ting, Xiong, Xingliang, Xiao, Na, Yan, Yizhong, Liu, Xiaoyang, Xie, Qi, Su, Xian, Chen, Maosheng, Peng, Jing, Wang, Siqi, Mei, Hua, Lin, Ge, Gong, Fei, Cheng, Lamei
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container_title International immunopharmacology
container_volume 130
creator Wang, Ting
Xiong, Xingliang
Xiao, Na
Yan, Yizhong
Liu, Xiaoyang
Xie, Qi
Su, Xian
Chen, Maosheng
Peng, Jing
Wang, Siqi
Mei, Hua
Lin, Ge
Gong, Fei
Cheng, Lamei
description •aCD19 Ab improved ovarian pathological structure and function of PCOS mice.•aCD19 Ab reduced splenic MZB cells and serum IgM level of PCOS mice.•aCD19 Ab reduced macrophage infiltration and TNF-α expression in ovaries of PCOS mice.•TNF-α promoted granulosa cell apoptosis. Immune dysregulation has been summarized as a critical factor in the occurrence and development of Polycystic ovary syndrome (PCOS), but potential mediators and mechanisms remain unclear. Our previous study showed that CD19+ B cells were involved in the pathogenesis of dehydroepiandrosterone (DHEA)-induced PCOS mice. Here, we studied the therapeutic potential of anti-CD19 antibody (aCD19 Ab) on DHEA-induced PCOS mice. The results showed that aCD19 Ab treatment improved ovarian pathological structure and function of PCOS mice, manifested by an increased number of corpus luteum, a decreased number of cystic follicles and atretic follicles, and regular estrus cycles. The aCD19 Ab treatment reduced the proportion of splenic CD21+ CD23low marginal zone B cells as well as the level of serum IgM and decreased the percentage of peripheral blood and splenic neutrophils. In particular, aCD19 Ab treatment reduced the apoptosis of granulosa cells and macrophage infiltration in ovarian secondary follicles of PCOS mice, as well as the expression of TNF-α in ovarian tissue and serum TNF-α levels. Moreover, we confirmed that TNF-α induced the apoptosis of human ovarian granulosa tumor cell line cells in vitro. Thus, our work demonstrates that aCD19 Ab treatment improves ovarian pathological phenotype and function by reducing local and systemic inflammation in PCOS mice, which may provide a novel insight into PCOS therapy.
doi_str_mv 10.1016/j.intimp.2024.111711
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Immune dysregulation has been summarized as a critical factor in the occurrence and development of Polycystic ovary syndrome (PCOS), but potential mediators and mechanisms remain unclear. Our previous study showed that CD19+ B cells were involved in the pathogenesis of dehydroepiandrosterone (DHEA)-induced PCOS mice. Here, we studied the therapeutic potential of anti-CD19 antibody (aCD19 Ab) on DHEA-induced PCOS mice. The results showed that aCD19 Ab treatment improved ovarian pathological structure and function of PCOS mice, manifested by an increased number of corpus luteum, a decreased number of cystic follicles and atretic follicles, and regular estrus cycles. The aCD19 Ab treatment reduced the proportion of splenic CD21+ CD23low marginal zone B cells as well as the level of serum IgM and decreased the percentage of peripheral blood and splenic neutrophils. 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subjects Anti-CD19 antibody
B lymphocytes
Inflammation
Polycystic ovary syndrome
TNF-α
title The therapeutic effect of anti-CD19 antibody on DHEA-induced PCOS mice
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