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Review
. 2019 May 28:10:1186.
doi: 10.3389/fmicb.2019.01186. eCollection 2019.

Human Cytomegalovirus Latency and Reactivation in Allogeneic Hematopoietic Stem Cell Transplant Recipients

Affiliations
Review

Human Cytomegalovirus Latency and Reactivation in Allogeneic Hematopoietic Stem Cell Transplant Recipients

Lauren Stern et al. Front Microbiol. .

Abstract

Human cytomegalovirus (HCMV) reactivation is a major infectious cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (HSCT). HCMV is a ubiquitous beta-herpesvirus which asymptomatically infects immunocompetent individuals but establishes lifelong latency, with the potential to reactivate to a life-threatening productive infection when the host immune system is suppressed or compromised. Opportunistic HCMV reactivation is the most common viral complication following engraftment after HSCT and is associated with a marked increase in non-relapse mortality, which appears to be linked to complex effects on post-transplant immune recovery. This minireview explores the cellular sites of HCMV latency and reactivation in HSCT recipients and provides an overview of the risk factors for HCMV reactivation post-HSCT. The impact of HCMV in shaping post-transplant immune reconstitution and its relationship with patient outcomes such as relapse and graft-versus-host disease will be discussed. Finally, we survey current and emerging strategies to prevent and control HCMV reactivation in HSCT recipients, with recent developments including adoptive T cell therapies to accelerate HCMV-specific T cell reconstitution and new anti-HCMV drug therapy for HCMV reactivation after HSCT.

Keywords: CMV; HCMV; HSCT; hematopoietic stem cell transplant; human cytomegalovirus; latency; reactivation.

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References

    1. Admiraal R., de Koning C. C. H., Lindemans C. A., Bierings M. B., Wensing A. M. J., Versluys A. B., et al. (2017). Viral reactivations and associated outcomes in the context of immune reconstitution after pediatric hematopoietic cell transplantation. J. Allergy Clin. Immunol. 140 1643–1650.e9. 10.1016/j.jaci.2016.12.992 - DOI - PubMed
    1. Aubert G., Hassan-Walker A. F., Madrigal J. A., Emery V. C., Morte C., Grace S., et al. (2001). Cytomegalovirus-specific cellular immune responses and viremia in recipients of allogeneic stem cell transplants. J. Infect. Dis. 184 955–963. 10.1086/323354 - DOI - PubMed
    1. Avdic S., McSharry B. P., Slobedman B. (2014). Modulation of dendritic cell functions by viral IL-10 encoded by human cytomegalovirus. Front. Microbiol. 5:337. 10.3389/fmicb.2014.00337 - DOI - PMC - PubMed
    1. Avetisyan G., Aschan J., Hägglund H., Ringdén O., Ljungman P. (2007). Evaluation of intervention strategy based on CMV-specific immune responses after allogeneic SCT. Bone Marrow Transplant. 40 865–869. 10.1038/sj.bmt.1705825 - DOI - PubMed
    1. Bhutani D., Dyson G., Manasa R., Deol A., Ratanatharathorn V., Ayash L., et al. (2015). Incidence, risk factors, and outcome of cytomegalovirus viremia and gastroenteritis in patients with gastrointestinal graft-versus-host disease. Biol. Blood Marrow Transplant. 21 159–164. 10.1016/j.bbmt.2014.10.004 - DOI - PMC - PubMed

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