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Control of Cytokines in Latent Cytomegalovirus Infection.
Chinta, Pearley; Garcia, Erica C; Tajuddin, Kiran Hina; Akhidenor, Naomi; Davis, Allyson; Faure, Lionel; Spencer, Juliet V.
Afiliação
  • Chinta P; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Garcia EC; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Tajuddin KH; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Akhidenor N; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Davis A; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Faure L; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
  • Spencer JV; Department of Biology, Texas Woman's University, P.O. Box 425799, 1000 Old Main Circle, Denton, TX 76204, USA.
Pathogens ; 9(10)2020 Oct 21.
Article em En | MEDLINE | ID: mdl-33096622
ABSTRACT
Human cytomegalovirus (HCMV) has evolved a number of mechanisms for long-term co-existence within its host. HCMV infects a wide range of cell types, including fibroblasts, epithelial cells, monocytes, macrophages, dendritic cells, and myeloid progenitor cells. Lytic infection, with the production of infectious progeny virions, occurs in differentiated cell types, while undifferentiated myeloid precursor cells are the primary site of latent infection. The outcome of HCMV infection depends partly on the cell type and differentiation state but is also influenced by the composition of the immune environment. In this review, we discuss the role of early interactions between HCMV and the host immune system, particularly cytokine and chemokine networks, that facilitate the establishment of lifelong latent infection. A better understanding of these cytokine signaling pathways could lead to novel therapeutic targets that might prevent latency or eradicate latently infected cells.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pathogens Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pathogens Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos