The ability of a cytomegalovirus ELISPOT assay to predict outcome of low-level CMV reactivation in hematopoietic cell transplant recipients
L El Haddad, E Ariza-Heredia, DP Shah… - The Journal of …, 2019 - academic.oup.com
The Journal of infectious diseases, 2019•academic.oup.com
Background Cytomegalovirus (CMV) infections in hematopoietic cell transplant (HCT)
recipients cause substantial morbidity and mortality. CMV cell-mediated immunity (CMV-
CMI) can be determined by levels of interferon gamma (IFN-γ) production using an enzyme-
linked immunospot (ELISPOT) CMV assay (T-SPOT. CMV assay). In this study, we evaluated
the ability of this assay to predict the outcome of low-level CMV reactivation in HCT
recipients. Methods We followed 55 HCT recipients with low-level CMV reactivation up to 8 …
recipients cause substantial morbidity and mortality. CMV cell-mediated immunity (CMV-
CMI) can be determined by levels of interferon gamma (IFN-γ) production using an enzyme-
linked immunospot (ELISPOT) CMV assay (T-SPOT. CMV assay). In this study, we evaluated
the ability of this assay to predict the outcome of low-level CMV reactivation in HCT
recipients. Methods We followed 55 HCT recipients with low-level CMV reactivation up to 8 …
Background
Cytomegalovirus (CMV) infections in hematopoietic cell transplant (HCT) recipients cause substantial morbidity and mortality. CMV cell-mediated immunity (CMV-CMI) can be determined by levels of interferon gamma (IFN-γ) production using an enzyme-linked immunospot (ELISPOT) CMV assay (T-SPOT.CMV assay). In this study, we evaluated the ability of this assay to predict the outcome of low-level CMV reactivation in HCT recipients.
Methods
We followed 55 HCT recipients with low-level CMV reactivation up to 8 weeks from enrollment. Progression to clinically significant CMV infection (CS-CMVi) was defined as a CMV load >1000 IU/mL or > 500 IU/mL in patients receiving matched related/autologous or matched unrelated transplants, respectively, and initiation of antiviral treatment.
Results
Progression to CS-CMVi occurred in 31 (56%) of the HCT recipients. Spot counts of CMV-specific pp65 and IE1 antigens were significantly lower in patients who had CS-CMVi than in patients who did not. On multivariate analysis, the ELISPOT CMV responses and steroids use were the only predictors of progression to CS-CMVi.
Conclusions
A strong association between low CMV-CMI and progression to CS-CMVi was observed in HCT recipients. The implementation of serial monitoring of CMV-CMI may identify patients at risk of progression to CS-CMVi that require antiviral therapy.
Oxford University Press