Literature DB >> 31212020

Persistent primary cytomegalovirus infection in a kidney transplant recipient: Multi-drug resistant and compartmentalized infection leading to graft loss.

Graciela Andrei1, Elisabet Van Loon2, Evelyne Lerut2, Jasper Victoor2, Björn Meijers2, Bert Bammens2, Ben Sprangers2, Sarah Gillemot3, Pierre Fiten3, Ghislain Opdenakker3, Katrien Lagrou4, Dirk Kuypers2, Robert Snoeck3, Maarten Naesens2.   

Abstract

Cytomegalovirus (CMV) is one of the most common opportunistic infections after transplantation. To prevent CMV infections, universal prophylaxis and pre-emptive therapy with ganciclovir or its prodrug valganciclovir is applied. However, prolonged antiviral therapy may result in drug-resistance emergence. We describe a case of a 43-year-old CMV-seronegative patient who underwent kidney transplantation from a CMV-seropositive donor and developed CMV disease despite valganciclovir prophylaxis. CMV viral load increased even though valgangiclovir dose was augmented and immunosuppressive therapy reduced. CMV genotyping revealed mutations in the viral UL97 protein kinase, explaining ganciclovir-resistant CMV infection. The viral load failed to respond to foscavir, cidofovir and CMV-neutralizing immunoglobulins. Kidney allograft dysfunction developed 3 months post-transplantation with a histopathologic diagnosis of CMV nephropathy and potentially concomitant T-cell mediated rejection. A transplantectomy was performed on day 164 post-transplantation since the patient had uncontrollable CMV disease associated with a circulating multidrug-resistant DNA polymerase-mutant virus. Detailed monitoring in this patient demonstrated hallmarks of complicated CMV disease: (i) relatively rapid evolution of drug-resistant CMV mutants in the setting of persistent high blood viral loads, (ii) emergence of viral drug-resistance linked to acute graft rejection, (iii) transient and, thereafter, lack of response to various anti-CMV treatments, (iv) compartmentalization and heterogeneity of CMV viral populations, (v) possible differential ability of viral mutants to cause disease in the graft, and (vi) detection of minor viral variants by next generation sequencing. Translational research platforms that provide rapid molecular genotyping for detection of CMV drug-resistance are essential in guiding CMV disease management in high-risk transplant recipients.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cytomegalovirus; Kidney transplantation; Multi drug-resistance; Viral compartmentalization

Mesh:

Substances:

Year:  2019        PMID: 31212020     DOI: 10.1016/j.antiviral.2019.06.004

Source DB:  PubMed          Journal:  Antiviral Res        ISSN: 0166-3542            Impact factor:   5.970


  2 in total

Review 1.  Advances in the genotypic diagnosis of cytomegalovirus antiviral drug resistance.

Authors:  Sunwen Chou
Journal:  Antiviral Res       Date:  2020-01-12       Impact factor: 5.970

2.  Virus-specific memory T cell responses unmasked by immune checkpoint blockade cause hepatitis.

Authors:  James A Hutchinson; Katharina Kronenberg; Paloma Riquelme; Jürgen J Wenzel; Gunther Glehr; Hannah-Lou Schilling; Florian Zeman; Katja Evert; Martin Schmiedel; Marion Mickler; Konstantin Drexler; Florian Bitterer; Laura Cordero; Lukas Beyer; Christian Bach; Josef Koestler; Ralph Burkhardt; Hans J Schlitt; Dirk Hellwig; Jens M Werner; Rainer Spang; Barbara Schmidt; Edward K Geissler; Sebastian Haferkamp
Journal:  Nat Commun       Date:  2021-03-04       Impact factor: 14.919

  2 in total

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