Chemokine Levels among Patients with Middle East Respiratory Syndrome Coronavirus Infection

Author:

Alhetheel Abdulkarim12ORCID,Albarrag Ahmed12,Shakoor Zahid12,Somily Ali12,Barry Mazin134ORCID,Altalhi Haifa1,Bakhrebah Muhammed5ORCID,Nassar Majed5ORCID,Alfageeh Mohamed5,Assiri Ayed6,Alfaraj Sarah7,Memish Ziad89ORCID

Affiliation:

1. King Saud University Medical City, Riyadh 11362, Saudi Arabia

2. Department of Pathology, College of Medicine, King Saud University, Riyadh 11451, Saudi Arabia

3. Department of Infectious Diseases, College of Medicine, King Saud University, Riyadh 11362, Saudi Arabia

4. Division of Infectious Diseases, Faculty of Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada

5. Advanced Diagnostics and Therapeutics Institute, Health Sector, King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia

6. Critical Care Unit, Prince Mohammed Bin Abdulaziz Hospital, Ministry of Health, Riyadh 11553, Saudi Arabia

7. Corona Center, Prince Mohammed Bin Abdulaziz Hospital, Ministry of Health, Riyadh 11553, Saudi Arabia

8. Research and Innovation Center, King Saud Medical City, Ministry of Health, Riyadh 11553, Saudi Arabia

9. College of Medicine, Alfaisal University, Riyadh 11553, Saudi Arabia

Abstract

Middle East respiratory syndrome coronavirus (MERS-CoV) is associated with significant morbidity and mortality due to intense pulmonary inflammation. Enhanced chemokine-mediated leukocyte infiltration in lungs has been linked with unfavorable outcomes with respect to the disease. This cross-sectional study assessed the levels of chemokines among 46 MERS-CoV-infected patients (19 asymptomatic and 27 symptomatic) and 52 healthy controls using a customized Luminex human chemokine magnetic multiplex panel. The plasma levels of interferon-inducible protein (IP)-10 (568.5 ± 114.7 vs. 55.19 ± 5.85 pg/mL; p < 0.0001), macrophage inflammatory protein (MIP)-1 alpha (MIP-1A) (30.78 ± 2.81 vs. 18.16 ± 0.91 pg/mL; p < 0.0001), MIP-1B (36.63 ± 4.25 vs. 25.26 ± 1.51 pg/mL; p < 0.003), monocyte chemoattractant protein (MCP)-1 (1267 ± 309.5 vs. 390.0 ± 35.51 pg/mL; p < 0.0002), and monokine-induced gamma interferon (MIG) (28.96 ± 3.93 vs. 16.29 ± 1.69 pg/mL; p < 0.001), interleukin (IL)-8 (147.9 ± 21.57 vs. 84.63 ± 10.62 pg/mL; p < 0.004) were significantly higher in symptomatic patients than healthy controls. Likewise, the levels of IP-10 (247.6 ± 80.09 vs. 55.19 ± 5.85 pg/mL; p < 0.0002) and MCP-1 (650.7 ± 149 pg/mL vs. 390 ± 35.51 pg/mL; p < 0.02) were also significantly higher in asymptomatic patients compared to healthy controls. However, no differences were observed in the plasma levels of MIP-1A, MIP-1B, MIG, and IL-8 between asymptomatic patients and uninfected controls. Conversely, the mean plasma levels of regulated on activation normal T cell expressed and secreted (RANTES) (3039 ± 301.0 vs. 4390 ± 223 pg/mL; p < 0.001) and eotaxin (176.9 ± 30.20 vs. 296.2 ± 28.11 pg/mL; p < 0.01) were significantly lower in symptomatic MERS-CoV-infected patients compared to healthy controls. Likewise, the levels of eotaxin (162.7 ± 21.60 vs. 296.2 ± 28.11 pg/mL; p < 0.01) were also significantly lower in asymptomatic patients. Interestingly, the level of MCP-1 (2139 ± 548.2 vs. 776.5 ± 165.3 pg/mL; p < 0.004) was significantly higher in deceased symptomatic patients compared to recovered symptomatic patients. MCP-1 was the only chemokine associated with a higher risk of mortality. Symptomatic MERS-CoV-infected patients had a significant elevation of plasma chemokines and elevated MCP-1 levels were found to be associated with fatal outcomes.

Funder

King Abdulaziz City for Science and Technology

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

Reference35 articles.

1. MERS coronavirus: Diagnostics, epidemiology and transmission;Mackay;Virol. J.,2015

2. (2023, May 25). Middle East Respiratory Syndrome: Global Summary and Assessment of Risk, 16 November 2022. Available online: https://www.who.int/publications/i/item/WHO-MERS-RA-2022.1.

3. Interleukins, from 1 to 37, and interferon-gamma: Receptors, functions, and roles in diseases;Akdis;J. Allergy Clin. Immunol.,2011

4. Chemokines and immunity;Palomino;Einstein,2015

5. Chemokines: A new classification system and their role in immunity;Zlotnik;Immunity,2000

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