Repeated intravesical platelet-rich plasma injections alleviate symptoms via T-cell modulation and mitochondrial dysfunction in non-ulcer interstitial cystitis/bladder pain syndrome

W Weilin Fang L Lin Liu X Xin Song J Jin Huang R Rong Lv Z Ziwei Li T Tingting Lv Z Zhikang Cai (Fundamental Science Center of Rare Earths) Z Zhong Wang (Alan G. MacDiarmid NanoTech Institute, University of Texas at Dallas) C Conghui Han J Jianwei Lv

Abstract

Abstract Repeated intravesical injections of autologous platelet-rich plasma (PRP) have shown promise in alleviating symptoms of non-ulcer interstitial cystitis bladder pain syndrome (IC/BPS), but the underlying mechanisms remain unclear. In this single-center prospective study, 80 patients received four monthly PRP injections, with outcomes assessed by symptom scales, urodynamic parameters, and immune indices in urine and serum. PRP significantly reduced 24-h micturition frequency, numeric rating scale (NRS), O’Leary, pelvic pain and urgency/frequency patient symptom scale (PUF), and self-rating anxiety scale (SAS) scores at post-treatment follow-ups (all p  < 0.05), while bladder capacity and voided volume remained unchanged. Serum and urinary inflammatory, iron metabolism, and oxidative stress markers were not significantly altered. PRP improved T-lymphocyte mitochondrial metabolic status, reducing CD4 +  and CD8 +  T-cell mitochondrial mass and decreasing CD8 +  effector memory (Tem) T-cell counts, CD8 +  Tem-MMP low , and CD8 +  PD-1 +  Tem counts after the fourth injection (all p  < 0.05). These immunological parameters positively correlated with symptom severity. Baseline NRS > 4 was associated with worse baseline profiles and selective post-treatment improvements, whereas global response assessment (GRA) stratification showed no significant differences. These findings indicate that repeated intravesical PRP alleviates IC/BPS-related pain and urinary symptoms primarily by reversing T-cell exhaustion and enhancing mitochondrial metabolic status, thus highlighting T-cell immunometabolic modulation as a key therapeutic mechanism.

Article Details

Volume / Issue Vol. 16, Issue 1
Published May 18, 2026
ISSN 2045-2322
Publisher Nature Portfolio

Journal Info

Scientific Reports

Nature Portfolio

ISSN: 2045-2322 Open Access Life Sciences

Authors (11)

W

Weilin Fang

L

Lin Liu

X

Xin Song

J

Jin Huang

R

Rong Lv

Z

Ziwei Li

T

Tingting Lv

Z

Zhikang Cai

Fundamental Science Center of Rare Earths

Z

Zhong Wang

Alan G. MacDiarmid NanoTech Institute, University of Texas at Dallas

C

Conghui Han

J

Jianwei Lv