Recurrent infections drive persistent bladder dysfunction and pain via sensory nerve sprouting and mast cell activity

Byron W. Hayes(Duke Medical Center), Hae Woong Choi(Korea University), Abhay P. S. Rathore(National University of Singapore), Chunjing Bao(Duke Medical Center), Jianling Shi(Duke Medical Center), Yul Huh(Duke Medical Center), Michael W. Kim(Duke Medical Center), Andrea Mencarelli(National University of Singapore), Pradeep Bist(National University of Singapore), Lai Guan Ng(Shanghai Jiao Tong University), Chuyan Shi(Shanghai Jiao Tong University), Joo Hwan Nho(Korea University), Aram Kim(Konkuk University), Hana Yoon(Ewha Womans University), Dong-Hoon Lim(Chosun University), Johanna L. Hannan(East Carolina University), J. Todd Purves(Duke Medical Center), Francis M. Hughes(Duke Medical Center), Ru‐Rong Ji(Duke University), Soman N. Abraham(National University of Singapore)
Science Immunology
March 1, 2024
Cited by 17Open Access
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Abstract

Urinary tract infections (UTIs) account for almost 25% of infections in women. Many are recurrent (rUTI), with patients frequently experiencing chronic pelvic pain and urinary frequency despite clearance of bacteriuria after antibiotics. To elucidate the basis for these bacteria-independent bladder symptoms, we examined the bladders of patients with rUTI. We noticed a notable increase in neuropeptide content in the lamina propria and indications of enhanced nociceptive activity. In mice subjected to rUTI, we observed sensory nerve sprouting that was associated with nerve growth factor (NGF) produced by recruited monocytes and tissue-resident mast cells. Treatment of rUTI mice with an NGF-neutralizing antibody prevented sprouting and alleviated pelvic sensitivity, whereas instillation of native NGF into naïve mice bladders mimicked nerve sprouting and pain behavior. Nerve activation, pain, and urinary frequency were each linked to the presence of proximal mast cells, because mast cell deficiency or treatment with antagonists against receptors of several direct or indirect mast cell products was each effective therapeutically. Thus, our findings suggest that NGF-driven sensory sprouting in the bladder coupled with chronic mast cell activation represents an underlying mechanism driving bacteria-independent pain and voiding defects experienced by patients with rUTI.


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