The potential association of CMV-specific CD8+ T lymphocyte reconstitution with the risk of CMV reactivation and persistency in post allogeneic stem cell transplant patients.

Autor: Shams El-Din AA; a Clinical and Chemical Pathology, Faculty of Medicine , Cairo University , Giza , Egypt., El-Desoukey NA; b Clinical and Chemical Pathology, The BMT Unit, Faculty of Medicine , Cairo University , Giza , Egypt., Amin Tawadrous DG; b Clinical and Chemical Pathology, The BMT Unit, Faculty of Medicine , Cairo University , Giza , Egypt., Fouad NMBE; a Clinical and Chemical Pathology, Faculty of Medicine , Cairo University , Giza , Egypt., Abdel-Mooti M; c The BMT Unit, Faculty of Medicine, NCI , Cairo University , Giza , Egypt., Hotar SF; d Clinical and Chemical Pathology, Egyptian Anti Doping Lab , International Medical Center , Cairo , Egypt.
Jazyk: angličtina
Zdroj: Hematology (Amsterdam, Netherlands) [Hematology] 2018 Sep; Vol. 23 (8), pp. 463-469. Date of Electronic Publication: 2018 Jan 09.
DOI: 10.1080/10245332.2017.1422686
Abstrakt: Objectives: development of cytomegalovirus (CMV)-specific CD8+ T cell response is crucial in preventing symptomatic CMV infection specially, in stem cell transplant (SCT) patients. The aim of this study was to evaluate CMV-specific CD8+ T cell reconstitution in allogeneic SCT recipients and to study the possible association between CMV-specific CD8+ T cell recovery with protection from CMV reactivation and persistency.
Methods: Human leuKocyte antigen (HLA)-tetramers were used for CMV-specific CD8+ cell quantitation by Flow cytometry in twenty post-allogeneic SCT patients.
Results: Nine patients (45%) developed rapid recovery of CMV-specific CD8+ cells, among them; 7 patients (78%) had no CMV reactivation in the first 95 days post-transplant. Five patients had developed persistent CMV viremia; all of them had not developed CMV-specific CD8+ recovery till day 95 post-transplant. Patients with persistent CMV viremia had a statistically significant lower means of CMV-specific CD8+ percent and absolute count compared to those without persistent viremia (p = .001, .015), respectively.
Discussion: The incidence of CMV reactivation and persistency was higher among patients with delayed CMV-specific CD8+ reconstitution in the first 95 days post-transplant.
Conclusion: CMV-specific CD8+ cells can help in categorizing patients into risk groups: (early recovery/low risk) and (delayed recovery/increased risk), this tool may guide clinicians in the selection of patients who may profit from prophylactic antiviral therapy and frequent viral monitoring.
Databáze: MEDLINE
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