Role of Interleukin-1 Family Members and Signaling Pathways in KSHV Pathogenesis.

Kaposi’s sarcoma Kaposi’s sarcoma-associated herpesvirus interleukin-1 multicentric Castleman’s disease primary effusion lymphoma

Journal

Frontiers in cellular and infection microbiology
ISSN: 2235-2988
Titre abrégé: Front Cell Infect Microbiol
Pays: Switzerland
ID NLM: 101585359

Informations de publication

Date de publication:
2020
Historique:
received: 27 07 2020
accepted: 13 10 2020
entrez: 16 11 2020
pubmed: 17 11 2020
medline: 22 6 2021
Statut: epublish

Résumé

Kaposi's sarcoma-associated herpesvirus (KSHV) represents the etiological agent for several human malignancies, including Kaposi's sarcoma (KS), primary effusion lymphoma (PEL), and multicentric Castleman's disease (MCD), which are mostly seen in immunocompromised patients. In fact, KSHV has developed many strategies to hijack host immune response, including the regulation of inflammatory cytokine production. Interleukin-1 (IL-1) family represents a major mediator for inflammation and plays an important role in both innate and adaptive immunity. Furthermore, a broadening list of diseases has revealed the pathologic role of IL-1 mediated inflammation. In the current mini-review, we have summarized recent findings about how this oncogenic virus is able to manipulate the activities of IL-1 signaling pathway to facilitate disease progression. We also discuss the therapeutic potential of IL-1 blockade against KSHV-related diseases and several unsolved questions in this interesting field.

Identifiants

pubmed: 33194830
doi: 10.3389/fcimb.2020.587929
pmc: PMC7662392
doi:

Substances chimiques

Interleukin-1 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

587929

Informations de copyright

Copyright © 2020 Barrett, Chen, Dai, Plaisance-Bonstaff, Del Valle and Qin.

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Auteurs

Lindsey Barrett (L)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, United States.

Jungang Chen (J)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, United States.

Lu Dai (L)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, United States.

Karlie Plaisance-Bonstaff (K)

Department of Medicine, Louisiana State University Health Sciences Center, Louisiana Cancer Research Center, New Orleans, LA, United States.

Luis Del Valle (L)

Department of Pathology, Louisiana State University Health Sciences Center, Louisiana Cancer Research Center, New Orleans, LA, United States.

Zhiqiang Qin (Z)

Department of Pathology, Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences, Little Rock, AR, United States.

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