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Immune Expression in Children With Vesicoureteral Reflux: A Pilot Study.
Johnston, Ashley W; Routh, Jonathan C; Purves, J Todd; Wiener, John S; Sinani, Angela; Holl, Eda K.
Affiliation
  • Johnston AW; Division of Urologic Surgery, Department of Surgery, Duke University School of Medicine, Durham, NC. Electronic address: Ashley.wietsma@duke.edu.
  • Routh JC; Division of Urologic Surgery, Department of Surgery, Duke University School of Medicine, Durham, NC.
  • Purves JT; Division of Urologic Surgery, Department of Surgery, Duke University School of Medicine, Durham, NC.
  • Wiener JS; Division of Urologic Surgery, Department of Surgery, Duke University School of Medicine, Durham, NC.
  • Sinani A; Dept of Chemical and Biomolecular Engineering, University of Delaware, Newark, DE.
  • Holl EK; Division of Surgical Sciences, Department of Surgery, Duke University School of Medicine, Durham, NC.
Urology ; 148: 254-259, 2021 02.
Article in En | MEDLINE | ID: mdl-33049235
OBJECTIVE: To perform an exploratory, descriptive pilot study of the systemic and local immune environment in patients with vesicoureteral reflux (VUR) and bladder-bowel dysfunction (BBD). METHODS: Consecutive children with VUR undergoing intravesical ureteral reimplantation were enrolled. Patients were assessed for presence of BBD by reported patient history and validated questionnaire. Fresh blood and bladder tissue, collected at the time of surgery, were immediately processed for analysis. Immune cell compositions were determined via flow cytometry. Immune cell activation was also defined at the time of analysis. LegendPlex assay analysis was utilized to define levels of circulating chemokines and cytokines. RESULTS: A total of 7 patients were enrolled. Although percentages of circulating immune cells in the blood of those with VUR/BBD and VUR alone were similar, within bladder tissue, VUR/BBD demonstrated increased immune infiltrates compared to VUR alone. Bladder sample analysis showed that B cells, and Effector Memory and Naïve T cell percentages were significantly increased in VUR/BBD patients compared to VUR patients. T cell expression of PD1 was increased in bladder tissues of BBD/VUR. Additionally, analysis of circulating neutrophils displayed significantly increased upregulation of PDL-1 in patients with VUR/BBD vs those with VUR only. CONCLUSION: These pilot data suggest an immune-rich microenvironment is present within VUR. Severity of inflammation appeared to correlate with presence of BBD. This implies that targeting pelvic inflammation may be a novel therapy for children with VUR- or non-VUR-related BBD. Follow-up studies are currently underway.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vesico-Ureteral Reflux Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Urology Year: 2021 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vesico-Ureteral Reflux Type of study: Observational_studies / Prognostic_studies Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: En Journal: Urology Year: 2021 Document type: Article Country of publication: United States