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Clinical utility of a cytomegalovirus-specific T cell assay in assessing the risk of post-prophylaxis cytomegalovirus infection and post-treatment relapse.
Dioverti, Maria Veronica; Bhaimia, Eric; Yetmar, Zachary A; Melendez, Dante P; Misner, Lori; Beito, Elaine; Deziel, Paul J; Theel, Elitza S; Razonable, Raymund R.
Afiliación
  • Dioverti MV; Division of Infectious Diseases, Johns Hopkins University, Baltimore, Maryland, USA.
  • Bhaimia E; Division of Infectious Diseases, Rush University Medical Center, Chicago, USA.
  • Yetmar ZA; Division of Public Health, Infectious Diseases, and Occupational Medicine, Mayo Clinic, Rochester, Minnesota, USA.
  • Melendez DP; Division of Infectious Diseases, University of Utah Health Sciences Center, Salt Lake City, USA.
  • Misner L; Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota, USA.
  • Beito E; Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota, USA.
  • Deziel PJ; William J von Leibig Center for Transplantation and Clinical Regeneration, Mayo Clinic, Rochester, Minnesota, USA.
  • Theel ES; Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota, USA.
  • Razonable RR; Division of Public Health, Infectious Diseases and Occupational Medicine and the William J von Leibig Center for Transplantation and Clinical Regeneration, Mayo Clinic, Rochester, Minnesota, USA.
Clin Transplant ; 37(12): e15143, 2023 12.
Article en En | MEDLINE | ID: mdl-37805968
ABSTRACT

INTRODUCTION:

Cytomegalovirus (CMV) causes significant morbidity in solid organ transplant recipients (SOTR). Measuring cell-mediated immunity (CMI) may inform the risk of CMV infection after antiviral prophylaxis and predict relapse after CMV treatment.

METHODS:

We serially assessed CMV CMI using the QuantiFERON-CMV assay (QF-CMV; Qiagen, Germantown, MD) in two cohorts of SOTRs during valganciclovir prophylaxis and during treatment of CMV viremia. Results of CMI were correlated with post-prophylaxis CMV infection and post-treatment relapse, respectively.

RESULTS:

Only one (4.2%) of 24 CMV D+/R- patients demonstrated positive QF-CMV by the end of valganciclovir prophylaxis. Four (16.6%) patients developed post-prophylaxis CMV infection; all four had undetectable QF-CMV at end of prophylaxis. Among 20 patients treated for CMV infection, 18 (90%) developed QF-CMV levels >.2 IU/mL by end of antiviral treatment and none developed CMV relapse. In contrast, the single patient who relapsed after completing treatment had a CMV CMI <.2 IU/ml (p = .0036).

CONCLUSION:

Since CMV D+/R- SOTRs are unlikely to develop adequate CMV CMI while receiving valganciclovir prophylaxis, the utility of CMV CMI monitoring for risk stratification during time of prophylaxis had limited value. Conversely, CMV CMI testing may be a useful marker of the risk of CMV relapse after antiviral treatment.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Riñón / Infecciones por Citomegalovirus Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Transplant Asunto de la revista: TRANSPLANTE Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trasplante de Riñón / Infecciones por Citomegalovirus Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Clin Transplant Asunto de la revista: TRANSPLANTE Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos