Clinical Progression and Cytokine Profiles of Middle East Respiratory Syndrome Coronavirus Infection.
Identifieur interne : 000F47 ( PubMed/Corpus ); précédent : 000F46; suivant : 000F48Clinical Progression and Cytokine Profiles of Middle East Respiratory Syndrome Coronavirus Infection.
Auteurs : Eu Suk Kim ; Pyoeng Gyun Choe ; Wan Beom Park ; Hong Sang Oh ; Eun Jung Kim ; Eun Young Nam ; Sun Hee Na ; Moonsuk Kim ; Kyoung Ho Song ; Ji Hwan Bang ; Sang Won Park ; Hong Bin Kim ; Nam Joong Kim ; Myoung Don OhSource :
- Journal of Korean medical science [ 1598-6357 ] ; 2016.
English descriptors
- KwdEn :
- Adult, Aged, Body Temperature, Chemokine CXCL10 (blood), Chemokines (blood), Coronavirus Infections (blood), Coronavirus Infections (complications), Coronavirus Infections (pathology), Creatinine (blood), Cytokines (blood), Disease Progression, Dyspnea (etiology), Enzyme-Linked Immunosorbent Assay, Female, Humans, Hyperbaric Oxygenation, Interferon-gamma (blood), Interleukin-6 (blood), Leukocyte Count, Male, Middle Aged, Neutrophils (cytology), Prothrombin Time, Severity of Illness Index.
- MESH :
- chemical , blood : Chemokine CXCL10, Chemokines, Creatinine, Cytokines, Interferon-gamma, Interleukin-6.
- blood : Coronavirus Infections.
- complications : Coronavirus Infections.
- cytology : Neutrophils.
- etiology : Dyspnea.
- pathology : Coronavirus Infections.
- Adult, Aged, Body Temperature, Disease Progression, Enzyme-Linked Immunosorbent Assay, Female, Humans, Hyperbaric Oxygenation, Leukocyte Count, Male, Middle Aged, Prothrombin Time, Severity of Illness Index.
Abstract
Clinical progression over time and cytokine profiles have not been well defined in patients with Middle East respiratory syndrome coronavirus (MERS-CoV) infection. We included 17 patients with laboratory-confirmed MERS-CoV during the 2015 outbreak in Korea. Clinical and laboratory parameters were collected prospectively. Serum cytokine and chemokine levels in serial serum samples were measured using enzyme-linked immunosorbent assay. All patients presented with fever. The median time to defervescence was 18 days. Nine patients required oxygen supplementation and classified into severe group. In the severe group, chest infiltrates suddenly began to worsen around day 7 of illness, and dyspnea developed at the end of the first week and became apparent in the second week. Median time from symptom onset to oxygen supplementation was 8 days. The severe group had higher neutrophil counts during week 1 than the mild group (4,500 vs. 2,200/μL, P = 0.026). In the second week of illness, the severe group had higher serum levels of IL-6 (54 vs. 4 pg/mL, P = 0.006) and CXCL-10 (2,642 vs. 382 pg/mL, P < 0.001). IFN-α response was not observed in mild cases. Our data shows that clinical condition may suddenly deteriorate around 7 days of illness and the serum levels of IL-6 and CXCL-10 was significantly elevated in MERS-CoV patients who developed severe diseases.
DOI: 10.3346/jkms.2016.31.11.1717
PubMed: 27709848
Links to Exploration step
pubmed:27709848Le document en format XML
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<front><div type="abstract" xml:lang="en">Clinical progression over time and cytokine profiles have not been well defined in patients with Middle East respiratory syndrome coronavirus (MERS-CoV) infection. We included 17 patients with laboratory-confirmed MERS-CoV during the 2015 outbreak in Korea. Clinical and laboratory parameters were collected prospectively. Serum cytokine and chemokine levels in serial serum samples were measured using enzyme-linked immunosorbent assay. All patients presented with fever. The median time to defervescence was 18 days. Nine patients required oxygen supplementation and classified into severe group. In the severe group, chest infiltrates suddenly began to worsen around day 7 of illness, and dyspnea developed at the end of the first week and became apparent in the second week. Median time from symptom onset to oxygen supplementation was 8 days. The severe group had higher neutrophil counts during week 1 than the mild group (4,500 vs. 2,200/μL, P = 0.026). In the second week of illness, the severe group had higher serum levels of IL-6 (54 vs. 4 pg/mL, P = 0.006) and CXCL-10 (2,642 vs. 382 pg/mL, P < 0.001). IFN-α response was not observed in mild cases. Our data shows that clinical condition may suddenly deteriorate around 7 days of illness and the serum levels of IL-6 and CXCL-10 was significantly elevated in MERS-CoV patients who developed severe diseases.</div>
</front>
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<Title>Journal of Korean medical science</Title>
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<ArticleTitle>Clinical Progression and Cytokine Profiles of Middle East Respiratory Syndrome Coronavirus Infection.</ArticleTitle>
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<Abstract><AbstractText>Clinical progression over time and cytokine profiles have not been well defined in patients with Middle East respiratory syndrome coronavirus (MERS-CoV) infection. We included 17 patients with laboratory-confirmed MERS-CoV during the 2015 outbreak in Korea. Clinical and laboratory parameters were collected prospectively. Serum cytokine and chemokine levels in serial serum samples were measured using enzyme-linked immunosorbent assay. All patients presented with fever. The median time to defervescence was 18 days. Nine patients required oxygen supplementation and classified into severe group. In the severe group, chest infiltrates suddenly began to worsen around day 7 of illness, and dyspnea developed at the end of the first week and became apparent in the second week. Median time from symptom onset to oxygen supplementation was 8 days. The severe group had higher neutrophil counts during week 1 than the mild group (4,500 vs. 2,200/μL, P = 0.026). In the second week of illness, the severe group had higher serum levels of IL-6 (54 vs. 4 pg/mL, P = 0.006) and CXCL-10 (2,642 vs. 382 pg/mL, P < 0.001). IFN-α response was not observed in mild cases. Our data shows that clinical condition may suddenly deteriorate around 7 days of illness and the serum levels of IL-6 and CXCL-10 was significantly elevated in MERS-CoV patients who developed severe diseases.</AbstractText>
</Abstract>
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<AffiliationInfo><Affiliation>Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.</Affiliation>
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<Author ValidYN="Y"><LastName>Park</LastName>
<ForeName>Wan Beom</ForeName>
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