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Standardized monitoring of cytomegalovirus-specific immunity can improve risk stratification of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation

Wagner-Drouet, E (author)
Teschner, D (author)
Wolschke, C (author)
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Janson, D (author)
Schafer-Eckart, K (author)
Gartner, J (author)
Mielke, S (author)
Karolinska Institutet
Schreder, M (author)
Kobbe, G (author)
Kondakci, M (author)
Hilgendorf, I (author)
von Lilienfeld-Toal, M (author)
Klein, S (author)
Heidenreich, D (author)
Kreil, S (author)
Verbeek, M (author)
Grass, S (author)
Ditschkowski, M (author)
Gromke, T (author)
Koch, M (author)
Lindemann, M (author)
Hunig, T (author)
Schmidt, T (author)
Rascle, A (author)
Guldan, H (author)
Barabas, S (author)
Deml, L (author)
Wagner, R (author)
Wolff, D (author)
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 (creator_code:org_t)
2019-12-26
2021
English.
In: Haematologica. - : Ferrata Storti Foundation (Haematologica). - 1592-8721 .- 0390-6078. ; 106:2, s. 363-374
  • Journal article (peer-reviewed)
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  • Recurrence of cytomegalovirus reactivation remains a major cause of morbidity and mortality following allogeneic hematopoietic stem cell transplantation. Monitoring cytomegalovirus-specific cellular immunity using a standardized assay might improve the risk stratification of patients. A prospective multicenter study was conducted in 175 intermediate- and high-risk allogeneic hematopoietic stem cell transplant recipients under preemptive antiviral therapy. Cytomegalovirus-specific cellular immunity was measured using a standardized IFN-γ ELISpot assay (T-Track® CMV). Primary aim was to evaluate the suitability of measuring cytomegalovirus-specific immunity after end of treatment for a first cytomegalovirus reactivation to predict recurrent reactivation. 40/101 (39.6%) patients with a first cytomegalovirus reactivation experienced recurrent reactivations, mainly in the high-risk group (cytomegalovirus-seronegative donor/cytomegalovirus-seropositive recipient). The positive predictive value of T-Track® CMV (patients with a negative test after the first reactivation experienced at least one recurrent reactivation) was 84.2% in high-risk patients. Kaplan-Meier analysis revealed a higher probability of recurrent cytomegalovirus reactivation in high-risk patients with a negative test after the first reactivation (hazard ratio 2.73; p=0.007). Interestingly, a post-hoc analysis considering T-Track® CMV measurements at day 100 post-transplantation, a time point highly relevant for outpatient care, showed a positive predictive value of 90.0% in high-risk patients. Our results indicate that standardized cytomegalovirus-specific cellular immunity monitoring may allow improved risk stratification and management of recurrent cytomegalovirus reactivation after hematopoietic stem cell transplantation. This study was registered at www.clinicaltrials.gov as #NCT02156479.

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