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Viral specific T cell therapy in kidney transplant recipients - A single-center experience.
Anand, Manish; Nysather, Jake; McGraw, Gregory; Apewokin, Senu; Khoury, Ruby; Grimley, Michael S; Bumb, Shalini; Govil, Amit.
Afiliación
  • Anand M; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
  • Nysather J; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
  • McGraw G; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
  • Apewokin S; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
  • Khoury R; Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Grimley MS; Department of Pediatrics, Cincinnati Children's Hospital, Cincinnati, Ohio, USA.
  • Bumb S; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
  • Govil A; Department of Internal Medicine, University of Cincinnati Medical Center, Cincinnati, Ohio, USA.
Transpl Infect Dis ; 25(6): e14179, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37910558
BACKGROUND: Viral infections such as adenovirus (ADV), BK virus (BKV), and cytomegalovirus (CMV) after kidney transplantation negatively impact outcomes in transplant recipients despite advancements in screening and antiviral therapy. We describe our experience of using the virus-specific T cell therapy (VSTs) in kidney transplant recipients (KTR) at our transplant center. METHODS: This is a retrospective, single center review of KTR with ADV, BKV and CMV infections between June 2021 and December 2022. These patients received third party VSTs as part of the management of infections. The immunosuppression, details of infection and outcome data were obtained from electronic medical records. RESULTS: Two cases of ADV infection resolved after one infusion of VSTs. The response rate of BKV and CMV infection was not as robust with close to 50% reduction in median viral load after VSTs. Out of 23 patients, two patients developed chronic allograft nephropathy from membranoproliferative glomerulonephritis and acute rejection. CONCLUSION: Patients that are resistant to antivirals or who have worsening viremia despite conventional management may benefit from VSTs therapy to treat underlying viral infection. Additional studies are needed to ascertain efficacy and short- and long-term risks secondary to VSTs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_sistemas_informacao_saude Asunto principal: Infecciones Tumorales por Virus / Trasplante de Riñón / Virus BK / Infecciones por Citomegalovirus / Infecciones por Polyomavirus Límite: Humans Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_sistemas_informacao_saude Asunto principal: Infecciones Tumorales por Virus / Trasplante de Riñón / Virus BK / Infecciones por Citomegalovirus / Infecciones por Polyomavirus Límite: Humans Idioma: En Revista: Transpl Infect Dis Asunto de la revista: TRANSPLANTE Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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