| Literature DB >> 34153157 |
Patricia Suàrez-Fernández1, Alberto Utrero-Rico1, Virginia Sandonis2, Estéfani García-Ríos2, Daniel Arroyo-Sánchez1,3, Mario Fernández-Ruiz1,4, Amado Andrés5, Natalia Polanco5, Cecilia González-Cuadrado1, Patricia Almendro-Vázquez1, Pilar Pérez-Romero2, José María Aguado1,4, Estela Paz-Artal1,3,6, Rocío Laguna-Goya1,3.
Abstract
Primary infection and/or reactivation of cytomegalovirus (CMV) in kidney transplant recipients (KTR) favor rejection and mortality. T follicular helper cells (TFH) could contribute to protection against CMV. Circulatory TFH (cTFH) were studied pretransplant and early posttransplant in 90 CMV seropositive KTR not receiving antithymocyte globulin or antiviral prophylaxis, followed-up for 1 year. Patients who presented CMV infection had significantly lower cTFH and activated cTFH pretransplant and early posttransplant. Pretransplant activated cTFH were also lower within patients who developed CMV disease. Pre- and 14 days posttransplant activated cTFH were an independent protective factor for CMV infection (HR 0.41, p = .01; and 0.52, p = .02, respectively). KTR with low cTFH 7 days posttransplant (<11.9%) had lower CMV infection-free survival than patients with high cTFH (28.2% vs. 67.6%, p = .002). cTFH were associated with CMV-specific neutralizing antibodies (Nabs). In addition, IL-21 increased interferon-γ secretion by CMV-specific CD8+ T cells in healthy controls. Thus, we show an association between cTFH and lower incidence of CMV infection, probably through their cooperation in CMV-specific Nab production and IL-21-mediated enhancement of CD8+ T cell activity. Moreover, monitoring cTFH pre- and early posttransplant could improve CMV risk stratification and help select KTR catalogued at low/intermediate risk who could benefit from prophylaxis.Entities:
Keywords: basic (laboratory) research / science; flow cytometry; immunobiology; infection and infectious agents - viral: Cytomegalovirus (CMV); infectious disease; kidney transplantation / nephrology; translational research / science
Mesh:
Year: 2021 PMID: 34153157 DOI: 10.1111/ajt.16725
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086