Blood · 2010 · 187 citations · 40 references
Life SciencesImmunologyInfectious DiseasesStem Cell TransplantationTransplant ImmunologyVirologyT Cell ActivationT Cell BiologyT Cell DifferentiationTransplant Infectious ComplicationsTransplant RejectionViral InfectionsAllogeneic Stem Cell TherapyCellular Immune Response To VirusesCytomegalovirus DiseaseCytomegalovirus PersistenceGamma Delta T Cell DifferentiationGamma-delta T Cell DevelopmentPost-transplant Cytomegalovirus Infection
Reactivation of cytomegalovirus (CMV) remains a serious complication after allogeneic stem cell transplantation, but the role of γδ T cells is undefined. We have studied the immune reconstitution of Vδ2negative (Vδ2neg) γδ T cells, including Vδ1 and Vδ3 subsets and Vδ2positive (Vδ2pos) γδ T cells in 40 patients during the first 24 months after stem cell transplantation. Significant long-term expansions of Vδ2neg but not Vδ2pos γδ T cells were observed during CMV reactivation early after transplantation, suggesting direct involvement of γδ T cells in anti-CMV immune responses. Similarly, significantly higher numbers of Vδ2neg γδ T cells were detected in CMV-seropositive healthy persons compared with seronegative donors; the absolute numbers of Vδ2pos cells were not significantly different. The expansion of Vδ2neg γδ T cells appeared to be CMV-related because it was absent in CMV-negative/Epstein-Barr virus-positive patients. T-cell receptor-δ chain determining region 3 spectratyping of Vδ2neg γδ T cells in healthy subjects and patients showed restricted clonality. Polyclonal Vδ2neg cell lines generated from CMV-seropositive healthy donors and from a recipient of a graft from a CMV-positive donor lysed CMV-infected targets in all cases. Our study shows new evidence for role of γδ T cells in the immune response to CMV reactivation in transplantation recipients.
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Mónica Gumá, Ana Angulo, Carlos Vilches et al. · Blood · 2004 · 844 citations · Full text
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Helmut R. Salih, Holger Antropius, Friederike Gieseke et al. · Blood · 2003 · 532 citations
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