Cytokine profile and disease severity in patients with COVID-19

被引:147
作者
Ghazavi, Ali [1 ,2 ,3 ]
Ganji, Ali [1 ,4 ]
Keshavarzian, Nafiseh [1 ]
Rabiemajd, Somayeh [1 ]
Mosayebi, Ghasem [1 ,4 ]
机构
[1] Arak Univ Med Sci, Sch Med, Dept Immunol & Microbiol, Arak, Iran
[2] Arak Univ Med Sci, Tradit & Complementary Med Res Ctr TCMRC, Arak, Iran
[3] Arak Univ Med Sci, Infect Dis Res Ctr IDRC, Arak, Iran
[4] Arak Univ Med Sci, Mol & Med Res Ctr, Arak, Iran
关键词
COVID-19; Cytokines; Disease severity; INFLAMMATORY RESPONSE; T-CELLS; CORONAVIRUS;
D O I
10.1016/j.cyto.2020.155323
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytokine dysregulation is the proposed mechanism for Coronavirus disease 2019 (COVID-19). The aim of this study was to evaluate the serum levels of interferon (IFN)-gamma, interleukin (IL)-5, IL-8, Il-9, IL-17, TGF-beta and IFN-gamma in patients infected with SARS-CoV-2. The study was conducted between 63 adult patients with COVID-19 and compared with 33 age and gender-matched healthy subjects as controls. The age range in both groups was 50-70 years. The patients were classified into mild group (33 patients) and severe group (30 patients). Serum samples were collected from all participants and tested for the cytokine levels by ELISA (enzyme-linked immunosorbent assay) method. Statistical analysis was performed using the one-way ANOVA. The mean serum levels of IFN-gamma, TGF-beta, IL-17 and IL-8 in the COVID-19 patients were significantly higher than those observed in the control group. A comparison of between the mild and severe groups showed significant differences in TGF-beta levels. The mean concentration of serum IL-5 and IL-9 in patients with COVID-19 did not differ from those in the control group. Systemic IL-17 levels correlated positively and significantly with TGF-beta in patients with COVID-19. Th1 (IFN-gamma), Treg (TGF-beta), and Th17 (IL-17) cytokines concentration were increased in COVID-19 patients. Interferon-gamma and IL-17 are involved in inducing and mediating proinflammatory responses. Our data suggest that TGF-beta can be used as a predictive factor of disease severity in patients with COVID-19.
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页数:5
相关论文
共 27 条
[1]  
Bhargava P., 2020, CANC RES STAT TREAT, V3, P65
[2]   Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19 [J].
Blanco-Melo, Daniel ;
Nilsson-Payant, Benjamin E. ;
Liu, Wen-Chun ;
Uhl, Skyler ;
Hoagland, Daisy ;
Moller, Rasmus ;
Jordan, Tristan X. ;
Oishi, Kohei ;
Panis, Maryline ;
Sachs, David ;
Wang, Taia T. ;
Schwartz, Robert E. ;
Lim, Jean K. ;
Albrecht, Randy A. ;
tenOever, Benjamin R. .
CELL, 2020, 181 (05) :1036-+
[3]   Immunologic dissonance: A continuing evolution in our understanding of the systemic inflammatory response syndrome (SIRS) and the multiple organ dysfunction syndrome (MODS) [J].
Bone, RC .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (08) :680-687
[4]   Cellular Stress in the Context of an Inflammatory Environment Supports TGF-β-Independent T Helper-17 Differentiation [J].
Brucklacher-Waldert, Verena ;
Ferreira, Cristina ;
Stebegg, Marisa ;
Fesneau, Olivier ;
Innocentin, Silvia ;
Marie, Julien C. ;
Veldhoen, Marc .
CELL REPORTS, 2017, 19 (11) :2357-2370
[5]   Regulatory T Cells in Arterivirus and Coronavirus Infections: Do They Protect Against Disease or Enhance it? [J].
Cecere, Thomas E. ;
Todd, S. Michelle ;
LeRoith, Tanya .
VIRUSES-BASEL, 2012, 4 (05) :833-846
[6]  
Chadwick D.J., 2008, T CELL SUBSETS INFEC
[7]   A potential treatment of COVID-19 with TGF-β blockade [J].
Chen, WanJun .
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2020, 16 (11) :1954-1955
[8]  
Conti P, 2020, J BIOL REG HOMEOS AG, V34, P327, DOI 10.23812/CONTI-E
[9]  
Danesh A., 2007, J INTERFERON CYTOKIN, V27, P1043
[10]   Increased expression of CD8 marker on T -cells in COVID-19 patients [J].
Ganji, Ali ;
Farahani, Iman ;
Khansarinejad, Behzad ;
Ghazavi, Ali ;
Mosayebi, Ghasem .
BLOOD CELLS MOLECULES AND DISEASES, 2020, 83