Changes in chemokine and growth factor levels may be useful biomarkers for monitoring disease severity in COVID-19 patients; a pilot study

被引:5
作者
Wolszczak-Biedrzycka, Blanka [1 ]
Dorf, Justyna [2 ]
Wojewodzka-Zelezniakowicz, Marzena [3 ]
Zendzian-Piotrowska, Malgorzata [4 ]
Dymicka-Piekarska, Violetta [2 ]
Matowicka-Karna, Joanna [2 ]
Maciejczyk, Mateusz [4 ]
机构
[1] Univ Warmia & Mazury, Dept Psychol & Sociol Hlth & Publ Hlth, Olsztyn, Poland
[2] Med Univ Bialystok, Dept Clin Lab Diag, Bialystok, Poland
[3] Med Univ Bialystok, Dept Emergency Med & Disasters, Bialystok, Poland
[4] Med Univ Bialystok, Dept Hyg Epidemiol & Ergon, Bialystok, Poland
关键词
chemokines; growth factors; COVID-19; MEWS score; SARS-CoV-2; CYTOKINE STORM; INFECTION; MIGRATION; IP-10;
D O I
10.3389/fimmu.2023.1320362
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: The aim of the present study was to assess differences in the serum levels of chemokines and growth factors (GFs) between COVID-19 patients and healthy controls. The diagnostic utility of the analyzed proteins for monitoring the severity of the SARS-CoV- 2 infection based on the patients' MEWS scores was also assessed. Materials and methods: The serum levels of chemokines and growth factors were analyzed in hospitalized COVID-19 patients (50 women, 50 men) with the use of the Bio-Plex Pro (TM) Human Cytokine Screening Panel (Biorad) and the Bio-Plex Multiplex system. Results: The study demonstrated that serum levels of MIP-1 alpha, RANTES, Eotaxin, CTACK, GRO-alpha, IP-10, MIG, basic-FGF, HGF, SCGF-beta, G-CSF, M-CSF, SCF, MIF, LIF, and TRAIL were significant higher in COVID-19 patients than in the control group. The concentrations of CTACK, GRO-alpha, IP-10, MIG, basic-FGF, HGF, PDGF- BB, GM-CSF, SCF, LIF, and TRAIL were higher in asymptomatic/mildly symptomatic COVID-19 patients (stage 1) and COVID-19 patients with pneumonia without respiratory failure (stage 2). The receiver operating characteristic (ROC) analysis revealed that IP-10, MIF, MIG, and basic-FGF differentiated patients with COVID-19 from healthy controls with the highest sensitivity and specificity, whereas GM-CSF, basic-FGF, and MIG differentiated asymptomatic/mildly symptomatic COVID-19 patients (stage 1) from COVID-19 patients with pneumonia without respiratory failure (stage 2) with the highest sensitivity and specificity. Conclusions: MIG, basic-FGF, and GM-CSF can be useful biomarkers for monitoring disease severity in patients with COVID-19.
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页数:13
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共 66 条
[1]   CXC chemokines IP-10 and Mig expression and direct migration of pulmonary CD8+/CXCR3+T cells in the lungs of patients with HIV infection and T-cell alveolitis [J].
Agostini, C ;
Facco, M ;
Siviero, M ;
Carollo, D ;
Galvan, S ;
Cattelan, AM ;
Zambello, R ;
Trentin, L ;
Semenzato, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (04) :1466-1473
[2]   Chemokine: Receptor structure, interactions, and antagonism [J].
Allen, Samantha J. ;
Crown, Susan E. ;
Handel, Tracy M. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :787-820
[3]   The Chemokine MIG is Associated with an Increased Risk of COVID-19 Mortality in Mexican Patients [J].
Antonio Ochoa-Ramirez, Luis ;
Ramos-Payan, Rosalio ;
Reynaldo Jimenez-Gastelum, German ;
Rodriguez-Millan, Jose ;
Aguilar-Medina, Maribel ;
Jose Rios-Tostado, Juan ;
Ayala-Ham, Alfredo ;
Bermudez, Mercedez ;
Fidel Osuna-Ramos, Juan ;
Olimon-Andalon, Vicente ;
Salvador Velarde-Felix, Jesus .
IRANIAN JOURNAL OF IMMUNOLOGY, 2022, 19 (03) :311-320
[4]   Chemokine Receptor Crystal Structures: What Can Be Learned from Them? [J].
Arimont, Marta ;
Hoffmann, Carsten ;
de Graaf, Chris ;
Leurs, Rob .
MOLECULAR PHARMACOLOGY, 2019, 96 (06) :765-777
[5]  
Arsentieva N., 2021, Med. Immunol, V23, P311, DOI [10.15789/1563-0625-PCI-2312, DOI 10.15789/1563-0625-PCI-2312, 10.15789]
[6]   PREDICTIVE VALUE OF SPECIFIC CYTOKINES FOR LETHAL COVID-19 OUTCOME [J].
Arsentieva, N. A. ;
Liubimova, N. E. ;
Batsunov, O. K. ;
Korobova, Z. R. ;
Kuznetsova, R. N. ;
Rubinstein, A. A. ;
Stanevich, O., V ;
Lebedeva, A. A. ;
Vorobyov, E. A. ;
Vorobyova, S. V. ;
Kulikov, A. N. ;
Gavrilova, E. G. ;
Pevtcov, D. E. ;
Polushin, Yu S. ;
Shlyk, I., V ;
Totolian, A. A. .
INFEKTSIYA I IMMUNITET, 2022, 12 (05) :859-868
[7]   The Potential Role of Growth Differentiation Factor 15 in COVID-19: A Corollary Subjective Effect or Not? [J].
Babalghith, Ahmad O. ;
Al-Kuraishy, Hayder M. ;
Al-Gareeb, Ali, I ;
De Waard, Michel ;
Sabatier, Jean-Marc ;
Saad, Hebatallah M. ;
Batiha, Gaber El-Saber .
DIAGNOSTICS, 2022, 12 (09)
[8]   Serum biomarkers associated with SARS-CoV-2 severity [J].
Batista, Fabiani de Morais ;
Moreira Puga, Marco Antonio ;
da Silva, Patricia Vieira ;
Oliveira, Roberto ;
Pereira dos Santos, Paulo Cesar ;
da Silva, Bruna Oliveira ;
Tatara, Mariana Bento ;
Tsuha, Daniel Henrique ;
dos Santos Pires, Maria Aparecida ;
Maymone Goncalves, Crhistinne Cavalheiro ;
Silva, Romulo Pessoa E. ;
Ferreira, Nathalia Tavares ;
de Barros Albuquerque, Amanda Pinheiro ;
Duarte, Giselle da Silva ;
Lopes Consolaro, Marcia Edilaine ;
Negrao, Fabio Juliano ;
Ferrari, Idalina Cristina ;
de Goes Cavalcanti, Luciano Pamplona ;
Trinta, Karen Soares ;
Ribeiro, Guilherme S. ;
Barreto de Melo Rego, Moacyr Jesus ;
Boyton, Rosemary J. ;
Siqueira, Andre Machado ;
Altmann, Daniel M. ;
Croda, Julio .
SCIENTIFIC REPORTS, 2022, 12 (01)
[9]   Alveolar compartmentalization of inflammatory and immune cell biomarkers in pneumonia-related ARDS [J].
Bendib, Ines ;
Beldi-Ferchiou, Asma ;
Schlemmer, Frederic ;
Surenaud, Mathieu ;
Maitre, Bernard ;
Plonquet, Anne ;
Carteaux, Guillaume ;
Razazi, Keyvan ;
Godot, Veronique ;
Hue, Sophie ;
Mekontso Dessap, Armand ;
de Prost, Nicolas .
CRITICAL CARE, 2021, 25 (01)
[10]   The non-ELR CXC chemokine encoded by human cytomegalovirus UL146 genotype 5 contains a C-terminal β-hairpin and induces neutrophil migration as a selective CXCR2 agonist [J].
Berg, Christian M. ;
Wedemeyer, Michael R. ;
Melynis, Motiejus ;
Schlimgen, Roman F. ;
Hansen, Lasse ;
Vabeno, Jon F. ;
Peterson, Francis ;
Volkman, Brian F. ;
Rosenkilde, Mette ;
Luettichau, Hans F. .
PLOS PATHOGENS, 2022, 18 (03)