Herpesvirus Infections Potentiated by Biologics.


Journal

Infectious disease clinics of North America
ISSN: 1557-9824
Titre abrégé: Infect Dis Clin North Am
Pays: United States
ID NLM: 8804508

Informations de publication

Date de publication:
06 2020
Historique:
entrez: 24 5 2020
pubmed: 24 5 2020
medline: 16 3 2021
Statut: ppublish

Résumé

Herpesviruses such as herpes simplex virus (HSV) type 1 and 2, varicella-zoster virus (VZV), and cytomegalovirus (CMV) maintain lifelong latency in the host after primary infection and can reactivate periodically either as asymptomatic viral shedding or as clinical disease. Immunosuppression, including biologic therapy, may increase frequency and severity of herpesvirus reactivation and infection. Licensed biologics are reviewed regarding their risks of potentiating HSV, VZV, and CMV reactivation and infection. Approaches to prophylaxis against HSV, VZV, and CMV infection or reactivation are discussed.

Identifiants

pubmed: 32444012
pii: S0891-5520(20)30008-8
doi: 10.1016/j.idc.2020.02.006
pii:
doi:

Substances chimiques

Biological Products 0
Immunosuppressive Agents 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

311-339

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Dora Y Ho (DY)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, 300 Pasteur Drive, Lane Building L-135, Stanford, CA 94305-5107, USA. Electronic address: doraywho@stanford.edu.

Kyle Enriquez (K)

Stanford University, 450 Serra Mall, Stanford, CA 94305, USA.

Ashrit Multani (A)

Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine at UCLA, 10833 Le Conte Avenue CHS 37-121, Los Angeles, CA 90095-1688, USA.

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Classifications MeSH