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Expression of CD80 and HLA-DR molecules on blood monocytes in patients with pulmonary tuberculosis

https://doi.org/10.15789/1563-0625-EOC-2348

Abstract

We examined expression pattern of CD80 and HLA-DR pro-inflammatory molecules on the monocytes in patients with pulmonary tuberculosis (TB), depending on the clinical form of the disease and susceptibility of the pathogen to anti-tuberculosis drugs. The study involved forty-five patients with newly diagnosed pulmonary TB (25 men and 20 women aged 18 to 55 years, average age — 44.0±12.4 years). The control group included 15 healthy donors with similar socio-demographic characteristics as in TB patients. Venous blood was used as biomaterial for assays. Studies of the monocyte immunophenotype were carried out by flow cytometry of whole blood cells using Cytoflex flow cytometer (Beckman Coulter, USA) with specific monoclonal antibodies (eBioscience, USA). We determined the content of cells expressing surface markers of monocytes, i.e., CD14, CD45, CD80, and HLA-DR. The results of this study were evaluated using SPSS Statistics 17.0 standard software package and Microsoft Excel. In the course of the study, we have suggested a working hypothesis that the monocytes in TB patients, still being in circulation, can express activation markers during their migration to inflammation focus, especially CD80 and HLA-DR molecules. Analysis of the total CD14+ monocyte number showed its decrease in all forms and variants of clinical course of pulmonary tuberculosis compared with the control group. Assessment of pro-inflammatory markers expressed on CD14 positive monocytes, i.e., HLA-DR activation marker and CD80 co-stimulatory molecule, showed that the number of monocytes with HLA-DR expression in all TB patients was higher than in healthy donors. HLA- DR expression on CD14+ monocytes in the group of patients with infiltrative TB proved to be 15% higher than in patients with disseminated TB. The expression of CD80 on CD14+ monocytes in TB patients showed no differences between the groups and varied within the normal range. Hence, an imbalance within monocyte population in patients with pulmonary tuberculosis, regardless of its clinical form and drug sensitivity of the pathogen is developed, due to decrease in total number of CD14+ cells, along with increased relative number of monocytes expressing HLA-DR activation marker (pro-inflammatory phenotype). Meanwhile, expression of the CD80 co-stimulatory molecule on monocytes was within normal values.

About the Authors

E. G. Churina
Siberian State Medical University; National Research Tomsk State University
Russian Federation

Elena G. Churina - PhD, MD (Medicine), Professor, Department of Pathophysiology, Siberian State Medical University; Professor, Department of Organic Chemistry, Leading Research Associate of Laboratory of Translational Cell and Molecular Biomedicine, National Research Tomsk State University.

634050, Tomsk, Moskovsky trakt, 2.

Phone: 7 (913) 806-07-00.


Competing Interests:

No



A. V. Popova
Siberian State Medical University
Russian Federation

Anjelika V. Popova - Postgraduate Student, Department of Pathophysiology, Siberian State Medical University.

Tomsk.


Competing Interests:

No



O. I. Urazova
Siberian State Medical University; Tomsk State University of Control Systems and Radioelectronics
Russian Federation

Olga I. Urazova - PhD, MD (Medicine), Professor, Corresponding Member, Russian Academy of Sciences, Head, Pathophysiology Division, Siberian State Medical University; Professor, Department of Complex Information Security of Computer Systems, Tomsk State University of Control Systems and Radioelectronics.

Tomsk.


Competing Interests:

No



M. R. Patysheva
National Research Tomsk State University; Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences
Russian Federation

Marina R. Patysheva - Junior Research Associate, Laboratory of Tumor Progression Biology, Cancer Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences; Junior Research Associate, Laboratory of Translational Cell and Molecular Biomedicine, National Research Tomsk State University.

Tomsk.


Competing Interests:

No



S. P. Chumakova
Siberian State Medical University
Russian Federation

Svetlana P. Chumakova - PhD, MD (Medicine) Professor, Department of Pathophysiology, Siberian State Medical University.

Tomsk.


Competing Interests:

No



Yu. V. Kolobovnikova
Siberian State Medical University
Russian Federation

Yulia V. Kolobovnikova - PhD, MD (Medicine), Professor, Department of Pathophysiology, Siberian State Medical University.

Tomsk.


Competing Interests:

No



E. O. Kazakova
National Research Tomsk State University
Russian Federation

Elena O. Kazakova - Junior Research Associate, Laboratory of Translational Cell and Molecular Biomedicine, National Research Tomsk State University.

Tomsk.


Competing Interests:

No



References

1. Yarilin A.A. Immunology: textbook. Moscow: GEOTAR-Media, 2010. 752 p.

2. Castano D., Garcia L.F., Rojas M. Increased frequency and cell death of CD16+ monocytes with Mycobacterium tuberculosis infection. Tuberculosis (Edinb)., 2011, Vol. 91, no. 5, pp. 348-360.

3. Gordon S., Pluddemann A., Estrada F.M. Macrophage heterogeneity in tissues: phenotypic diversity and functions. Immunol. Rev., 2014, Vol. 262, no. 1, pp. 36-55.

4. Grimaldi D., Louis S., Pene E, Sirgo G., Rousseau C., Claessens L. Vimeux Y.E., Cariou A., Mira J.P., Hosmalin A., Chiche J.D. Profound and persistent decrease of circulating dendritic cells is associated with ICU-acquired infection in patients with septic shock. Intensive Care Med., 2011, Vol. 37, no. 9, pp. 1438-1446.

5. Monneret G., Lepape A., Voirin N., Bohe J., Venet F., Debard A.L., 'Ihizy H., Bienvenu J., Gueyffier F., Vanhems P. Persisting low monocyte human leukocyte antigen-DR expression predicts mortality in septic shock Intensive. Care Med., 2006, Vol. 32, no. 8, pp. 1175-1183.

6. Monneret G., Venet F., Pachot A., Lepape A. Monitoring immune dysfunctions in the septic patient: a new skin for the old ceremony. Mol. Med., 2008, Vol. 14, no. 1/2, pp. 64-78.

7. Peyravian N., Gharib E., Moradi A., Mobahat M., Tarban P., Azimzadeh P., Nazemalhosseini-Mojarad E., Aghdaei H.A. Evaluating the expression level of co-stimulatory molecules CD 80 and CD 86 in different types of colon polyps. Curr. Res. Transl. Med., 2018, Vol. 66, no. 1, pp. 19-25.

8. Poehlmann H., Schefold J.C., Zuckermann-Becker H., Volk H.D., Meisel C. Phenotype changes and impaired function of dendritic cell subsets in patients with sepsis: a prospective observational analysis. Crit. Care., 2009, Vol. 13, no. 4, R119. doi: 10.1186/cc7969.

9. Sampath P., Moideen K., Ranganathan U.D., Bethunaickan R. Monocyte subsets: phenotypes and function in tuberculosis infection. Front. Immunol., 2018, Vol. 9, 1726. doi: 10.3389/fimmu.2018.01726.

10. Scarpa M., Brun P., Scarpa M., Morgan S., Porzionato A., Kotsafti A., Bortolami M., Buda A., Dina R., Macchi V., Sturniolo G.C., Rugge M., Bardini R., Castagliuolo I., Angriman I., Castoro C. CD80-CD28 signaling controls the progression of inflammatory colorectal carcinogenesis. Oncotarget, 2015, Vol. 6, no. 24, pp. 20058-20069.

11. Sica A., Erreni M., Allavena P., Porta C. Macrophage polarization in Pathology. Cell. Mol. Life Sci., 2015, Vol. 72, no. 1, pp. 4111-4126.

12. Tae A.G., Khaled C.M., Barakat H. Revealing the atomistic details behind the binding of B7-1 to CD28 and CTLA-4: A comprehensive protein-protein modelling study. Biochim. Biophys. Acta Gen. Subj., 2018, Vol. 1862, no. 12, pp. 2764-2778.

13. Venet F., Lukaszewicz A.C., Payen D., Hotchkiss R., Monneret G. Monitoring the immune response in sepsis: a rational approach to administration of immunoadjuvant therapies. Curr. Opin Immunol., 2013, Vol. 25, no. 4, pp. 477-483.

14. Wang L.X., Mei Z.Y., Zhou J.H., Yao Y.S., Li Y.H., Xu Y.H., Li J.X., Gao X.N., Zhou M.H., Jiang M.M., Gao L., Ding Y., Lu X.C., Shi J.L., Luo X.F., Wang J., Wang L.L., Qu C., Bai X.F., Yu L. Low dose decitabine treatment induces CD80 expression in cancer cells and stimulates tumor specific cytotoxic T lymphocyte responses. PLoS One, 2013, Vol. 8, no. 5, e62924. doi: 10.1371/journal.pone.0062924.

15. Zhuang Y., Peng H., Chen Y., Zhou S., Chen Y. Dynamic monitoring of monocyte HLA-DR expression for the diagnosis, prognosis, and prediction of sepsis. Front. Biosci. (Landmark Ed.), 2017, Vol. 22, pp. 1344-1354.


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For citations:


Churina E.G., Popova A.V., Urazova O.I., Patysheva M.R., Chumakova S.P., Kolobovnikova Yu.V., Kazakova E.O. Expression of CD80 and HLA-DR molecules on blood monocytes in patients with pulmonary tuberculosis. Medical Immunology (Russia). 2021;23(5):1183-1190. (In Russ.) https://doi.org/10.15789/1563-0625-EOC-2348

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ISSN 1563-0625 (Print)
ISSN 2313-741X (Online)