| Literature DB >> 32827084 |
Yuqian Liu1, Meng Tang1, Qin Zhang1, Cuican Li1, Rundong Lv1, Hanhui Min1, Xiaohui Zhou2,3,4.
Abstract
Chronic prostatitis/chronic pelvic pain syndromes (CP/CPPS) is a clinical tricky problem due to its enigmatic etiology, low cure rate, and high recurrence rate. The research on its pathogenesis has never stopped. In this experimental autoimmune prostatitis (EAP) model, male C57BL/6 mice were subcutaneously immunized with prostate extracts in an adequate adjuvant. For mice in the antibody intervention group, anti-T2 polyclonal antibodies were intraperitoneally injected during the induction of EAP. Animals were periodically monitored for pelvic pain. Hematoxylin and eosin staining was used to assess prostate inflammation. Tumor necrosis factor-α (TNF-α) levels in serum were measured by ELISA kits. The immunized animals developed prostatitis as a consequence of the immune response against prostate antigens. Pelvic pain thresholds were gradually decreased and TNF-α expression significantly increased. T2 plays an important role in the disease since polyclonal antibodies to T2 greatly ameliorated symptoms in animals induced for EAP. T2 peptide may represent the major autoantigen epitope in EAP, which could serve for a better understanding of the etiology of CP/CPPS.Entities:
Keywords: Autoantigen epitope; Autoimmune disease; Chronic prostatitis/chronic pelvic pain syndrome; T2 peptide
Year: 2020 PMID: 32827084 DOI: 10.1007/s10753-020-01326-6
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092