Identifying cytomegalovirus complications using the quantiferon-CMV assay after allogeneic hematopoietic stem cell transplantation

Michelle K. Yong, Paul U. Cameron, Monica Slavin, C. Orla Morrissey, Krystal Bergin, Andrew Spencer, David Ritchie, Allen C. Cheng, Assia Samri, Guislaine Carcelain, Brigitte Autran, Sharon R. Lewin

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

Background. A simple test to identify recovery of CMV-specific T-cell immunity following hematopoietic stem cell transplantation (HSCT) could assist clinicians in managing CMV-related complications. Methods. In an observational, multicenter, prospective study of 94 HSCT recipients we evaluated CMV-specific T-cell immunity at baseline, 3, 6, 9, and 12 months after transplant using the Quantiferon-CMV, an enzyme-linked immunosorbent spot assay (ELISpot), and intracellular cytokine staining. Results. At 3 months after HSCT, participants who developed CMV disease (n = 8) compared with CMV reactivation (n = 26) or spontaneous viral control (n = 25) had significantly lower CD8+ T-cell production of interferon-γ (IFN-γ) in response to CMV antigens measured by Quantiferon-CMV (P = .0008). An indeterminate Quantiferon-CMV result had a positive predictive value of 83% and a negative predictive value of 98% for identifying participants at risk of further CMV reactivation. Participants experiencing CMV reactivation compared with patients without CMV reactivation had a reduced proportion of polyfunctional (IFN-γ+/tumor necrosis factor a-positive) CD4+ and CD8+ T cells and a higher proportion of interleukin 2-secreting cells (P = .01 and P = .002, respectively). Conclusions. Quantifying CMV-specific T-cell immunity after HSCT can identify participants at increased risk of clinically relevant CMV-related outcomes.

Original languageEnglish
Pages (from-to)1684-1694
Number of pages11
JournalJournal of Infectious Diseases
Volume215
Issue number11
DOIs
StatePublished - 1 Jun 2017
Externally publishedYes

Keywords

  • Cytomegalovirus
  • Immunocompromised host
  • Stem cell transplantation
  • T-cell immunity
  • Viral immunity

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