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CXCR3 antagonist AMG487 ameliorates experimental autoimmune prostatitis by diminishing Th1 cell differentiation and inhibiting macrophage M1 phenotypic activation.

Xiaoliang HuaJiong ZhangShengdong GeHaoran LiuHe-Xi DuQingsong NiuXianguo ChenCheng YangLi ZhangChao-Zhao Liang
Published in: The Prostate (2022)
CXCR3 antagonist AMG487 could ameliorate the inflammatory changes and the pelvic pain of EAP mice by diminishing Th1 cell differentiation and inhibiting macrophage M1 phenotypic activation. Thus, the results imply that AMG487 has the potential as an effective therapeutic agent in the prevention and treatment of EAP.
Keyphrases
  • signaling pathway
  • adipose tissue
  • chronic pain
  • multiple sclerosis
  • pain management
  • cell migration
  • oxidative stress
  • neuropathic pain
  • mouse model
  • type diabetes
  • metabolic syndrome