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MERS-CoV infection in humans is associated with a pro-inflammatory Th1 and Th17 cytokine profile.
- Source :
-
Cytokine [Cytokine] 2018 Apr; Vol. 104, pp. 8-13. Date of Electronic Publication: 2018 Feb 02. - Publication Year :
- 2018
-
Abstract
- The Middle East respiratory syndrome coronavirus (MERS-CoV) has been recognized as a highly pathogenic virus to humans that infects the respiratory tract and is associated with high morbidity and mortality. Studies in animal models suggest that MERS-CoV infection induces a strong inflammatory response, which may be related to the severity of disease. Data showing the cytokine profiles in humans during the acute phase of MERS-CoV infection are limited. In this study, we have analyzed the profile of cytokine responses in plasma samples from patients with confirmed MERS-CoV infections (n = 7) compared to healthy controls (n = 13). The cytokine profiles, including T helper (Th) 1, Th2 and Th17 responses, were analyzed using cytometric bead array (CBA). A prominent pro-inflammatory Th1 and Th17 response was clearly seen in patients with MERS-CoV infection, with markedly increased concentrations of IFN-γ, TNF-α, IL-15 and IL-17 compared to controls. IL-12 expression levels showed no difference between patients with MERS-CoV infection and the healthy controls despite the significantly increased levels of IFN-α2 and IFN-γ (P < .01). No changes were observed in the levels of IL-2, IL-4, IL-5, IL-13, and TGF-α (P > .05). Our results demonstrate a marked pro-inflammatory cytokine response during the acute phase of MERS-CoV infection in humans.<br /> (Copyright © 2018 Elsevier Ltd. All rights reserved.)
- Subjects :
- Adult
Coronavirus Infections blood
Cytokines blood
Cytokines chemistry
Humans
Interferons blood
Interferons metabolism
Male
Middle Aged
Protein Structure, Secondary
Young Adult
Coronavirus Infections immunology
Coronavirus Infections virology
Cytokines metabolism
Middle East Respiratory Syndrome Coronavirus physiology
Th1 Cells metabolism
Th17 Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0023
- Volume :
- 104
- Database :
- MEDLINE
- Journal :
- Cytokine
- Publication Type :
- Academic Journal
- Accession number :
- 29414327
- Full Text :
- https://doi.org/10.1016/j.cyto.2018.01.025