Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Aug 23;24(17):13083.
doi: 10.3390/ijms241713083.

Macrophage-Derived Chemokine MDC/CCL22: An Ambiguous Finding in COVID-19

Affiliations

Macrophage-Derived Chemokine MDC/CCL22: An Ambiguous Finding in COVID-19

Zoia R Korobova et al. Int J Mol Sci. .

Abstract

Macrophage-derived chemokine (MDC/CCL22) is a chemokine of the C-C subfamily. It is involved in T-cellular maturation and migration. Our previous research shows that plasma CCL22/MDC tends to show a statistically significant depletion of concentrations in acute patients and convalescents when compared to healthy donors. In the current work, we investigate existing views on MDC/CCL22 dynamics in association with various pathologies, including respiratory diseases and, specifically, COVID-19. Additionally, we present our explanations for the observed decrease in MDC/CCL22 concentrations in COVID-19. The first hypothesis we provide implies that viral products bind to MDC/CCL22 and block its activity. Another explanation for this phenomenon is based on dendritic cells population and the inhibition of their function.

Keywords: COVID-19; MDC/CCL22; chemokines; macrophage-derived chemokine; novel coronavirus infection; post-COVID.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interests.

Figures

Figure 1
Figure 1
Possible mechanisms for lower MDC/CCL22 concentrations in COVID-19 patients’ plasma: (I) Decrease in MDC/CCL22 concentration associated with selective binding to SARS-CoV-2 viral peptides; (II) Restriction of MDC/CCL22 secretion by producer cells due to their functional failure.
Figure 2
Figure 2
Role of MDC/CCL22 in immunity and the SARS-CoV-2 infectious process. (I) MDC/CCL22 influence on T lymphocyte maturation in thymus via the CCR4 receptor. The presence of this chemokine also mediates an adequate balance between regulatory T cells and helper T cells, thus creating restrictions on inflammatory reactions. (II) SARS-CoV-2 influence on T cell maturation in thymus via depletion of MDC/CCL22: (A) decrease in MDC/CCL22 concentrations associated with selective binding to SARS-CoV-2 viral peptides; (B) restriction of MDC/CCL22 secretion by producer cells due to their functional failure.

References

    1. Liu Y.-C., Kuo R.-L., Shih S.-R. COVID-19: The first documented coronavirus pandemic in history. Biomed. J. 2020;43:328–333. doi: 10.1016/j.bj.2020.04.007. - DOI - PMC - PubMed
    1. Borczuk A.C., Yantiss R.K. The pathogenesis of coronavirus-19 disease. J. Biomed. Sci. 2022;29:87. doi: 10.1186/s12929-022-00872-5. - DOI - PMC - PubMed
    1. Borges do Nascimento I.J., O’Mathúna D.P., von Groote T.C., Abdulazeem H.M., Weerasekara I., Marusic A., Puljak L., Civile V.T., Zakarija-Grkovic I., Pericic T.P., et al. Coronavirus disease (COVID-19) pandemic: An overview of Systematic Reviews. BMC Infect. Dis. 2021;21:525. doi: 10.1186/s12879-021-06214-4. - DOI - PMC - PubMed
    1. Merad M., Blish C.A., Sallusto F., Iwasaki A. The immunology and immunopathology of COVID-19. Science. 2022;375:1122–1127. doi: 10.1126/science.abm8108. - DOI - PubMed
    1. Salamanna F., Maglio M., Landini M.P., Fini M. Body Localization of ACE-2: On the Trail of the Keyhole of SARS-CoV-2. Front. Med. 2020;7:594495. doi: 10.3389/fmed.2020.594495. - DOI - PMC - PubMed

LinkOut - more resources