Immunopathologic Effects of Prednisolone and Cyclosporine A on Feline Immunodeficiency Virus Replication and Persistence.


Journal

Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722

Informations de publication

Date de publication:
30 08 2019
Historique:
received: 31 07 2019
revised: 22 08 2019
accepted: 27 08 2019
entrez: 5 9 2019
pubmed: 5 9 2019
medline: 15 9 2020
Statut: epublish

Résumé

Feline immunodeficiency virus (FIV) induces opportunistic disease in chronically infected cats, and both prednisolone and cyclosporine A (CsA) are clinically used to treat complications such as lymphoma and stomatitis. However, the impact of these compounds on FIV infection are still unknown and understanding immunomodulatory effects on FIV replication and persistence is critical to guide safe and effective therapies. To determine the immunologic and virologic effects of prednisolone and CsA during FIV infection, FIV-positive cats were administered immunosuppressive doses of prednisolone (2 mg/kg) or CsA (5 mg/kg). Both prednisolone and CsA induced acute and transient increases in FIV DNA and RNA loads as detected by quantitative PCR. Changes in the proportion of lymphocyte immunophenotypes were also observed between FIV-infected and naïve cats treated with CsA and prednisolone, and both treatments caused acute increases in CD4+ lymphocytes that correlated with increased FIV RNA. CsA and prednisolone also produced alterations in cytokine expression that favored a shift toward a Th2 response. Pre-treatment with CsA slightly enhanced the efficacy of antiretroviral therapy but did not enhance clearance of FIV. Results highlight the potential for drug-induced perturbation of FIV infection and underscore the need for more information regarding immunopathologic consequences of therapeutic agents on concurrent viral infections.

Identifiants

pubmed: 31480322
pii: v11090805
doi: 10.3390/v11090805
pmc: PMC6783960
pii:
doi:

Substances chimiques

Cytokines 0
Immunosuppressive Agents 0
Cyclosporine 83HN0GTJ6D
Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIAID NIH HHS
ID : R01AI25825
Pays : United States

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Auteurs

Craig Miller (C)

Department of Veterinary Pathobiology, Oklahoma State University, Stillwater, OK 74078, USA. craig.miller@okstate.edu.

Jordan Powers (J)

Department of Microbiology, Immunology, Pathology, Colorado State University, Fort Collins, CO 80523, USA.

Esther Musselman (E)

Department of Microbiology, Immunology, Pathology, Colorado State University, Fort Collins, CO 80523, USA.

Ryan Mackie (R)

Department of Microbiology, Immunology, Pathology, Colorado State University, Fort Collins, CO 80523, USA.

John Elder (J)

Department of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA 92037, USA.

Sue VandeWoude (S)

Department of Microbiology, Immunology, Pathology, Colorado State University, Fort Collins, CO 80523, USA.

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