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The Serum ACE2, CTSL, AngII, and TNFα Levels after COVID-19 and mRNA Vaccines: The Molecular Basis.

Authors :
Pencheva, Mina
Bozhkova, Martina
Kalchev, Yordan
Petrov, Steliyan
Baldzhieva, Alexandra
Kalfova, Teodora
Dichev, Valentin
Keskinova, Donka
Genova, Silvia
Atanasova, Mariya
Murdzheva, Mariana
Source :
Biomedicines; Dec2023, Vol. 11 Issue 12, p3160, 20p
Publication Year :
2023

Abstract

Background: The SARS-CoV-2 virus as well as the COVID-19 mRNA vaccines cause an increased production of proinflammatory cytokines. Aim: We investigated the relationship between ACE2, CTSL, AngII, TNFα and the serum levels of IL-6, IL-10, IL-33, IL-28A, CD40L, total IgM, IgG, IgA and absolute count of T- and B-lymphocytes in COVID-19 patients, vaccinees and healthy individuals. Methods: We measured the serum levels ACE2, AngII, CTSL, TNFα and humoral biomarkers (CD40L, IL-28A, IL-10, IL-33) by the ELISA method. Immunophenotyping of lymphocyte subpopulations was performed by flow cytometry. Total serum immunoglobulins were analyzed by the turbidimetry method. Results: The results established an increase in the total serum levels for ACE2, CTSL, AngII and TNFα by severely ill patients and vaccinated persons. The correlation analysis described a positive relationship between ACE2 and proinflammatory cytokines IL-33 (r = 0.539) and CD40L (r = 0.520), a positive relationship between AngII and CD40L (r = 0.504), as well as between AngII and IL-33 (r = 0.416), and a positive relationship between CTSL, total IgA (r = 0.437) and IL-28A (r = 0.592). Correlation analysis confirmed only two of the positive relationships between TNFα and IL-28A (r = 0.491) and CD40L (r = 0.458). Conclusions: In summary, the findings presented in this study unveil a complex web of interactions within the immune system in response to SARS-CoV-2 infection and vaccination. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22279059
Volume :
11
Issue :
12
Database :
Complementary Index
Journal :
Biomedicines
Publication Type :
Academic Journal
Accession number :
174402360
Full Text :
https://doi.org/10.3390/biomedicines11123160