Clinical utility of a cytomegalovirus‐specific T cell assay in assessing the risk of post‐prophylaxis cytomegalovirus infection and post‐treatment relapse

Author:

Dioverti Maria Veronica1ORCID,Bhaimia Eric2ORCID,Yetmar Zachary A.3ORCID,Melendez Dante P.4,Misner Lori5,Beito Elaine5,Deziel Paul J.6,Theel Elitza S.5,Razonable Raymund R.7ORCID

Affiliation:

1. Division of Infectious Diseases Johns Hopkins University Baltimore Maryland USA

2. Division of Infectious Diseases Rush University Medical Center Chicago USA

3. Division of Public Health, Infectious Diseases, and Occupational Medicine Mayo Clinic Rochester Minnesota USA

4. Division of Infectious Diseases University of Utah Health Sciences Center Salt Lake City USA

5. Division of Clinical Microbiology Mayo Clinic Rochester Minnesota USA

6. William J von Leibig Center for Transplantation and Clinical Regeneration Mayo Clinic Rochester Minnesota USA

7. 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

Abstract

AbstractIntroductionCytomegalovirus (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.MethodsWe 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.ResultsOnly 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).ConclusionSince 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.

Funder

QIAGEN

Publisher

Wiley

Subject

Transplantation

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