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Netosis-forming ability of neutrophils in children with respiratory tuberculosis

[Pediatrics]
Anna Mordyk; Dmitry Georgyevich Novikov; Alexander Nikolaevich Zolotov; Maria Romanova; Nikolay Aleksandrovich Kirichenko; Alexander Olegovich Ptukhin;

The aim of the study was to evaluate the NETosis-forming ability of peripheral blood neutrophils in children with respiratory tuberculosis.

Using fluorescent microscopy, the percentage of intact neutrophils, activated neutrophils, early netosis cells, cloud shaped NETs, and filamentous NETs was calculated.

Neutrophils in the study group formed cloud-shaped NETs significantly more often (p=0.0007). The median proportion of this type of trap in the control group (with a negative reaction to tuberculin) was 4.9 %, and in the group with tuberculosis – 15.7 %. The proportion of cloud-shaped NETs in the tuberculosis group was higher than the proportion of filamentous NETs. Thus, the neutrophils of children with TB formed mainly cloudy NETs, which is not characteristic of healthy children, whose neutrophils more often were formed by filamentous NETs.

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References:
1. Bagcchi S. WHO’s Global Tuberculosis Report 2022. Lancet Microbe. 2023;4(1):e20. https://doi.org/10.1016/S2666-5247(22)00359-7
2. Jiao W. W., Liu Z. G., Han R., Zhao X. Q., Dong F. [et al.]. Prevalence of drug resistant Mycobacterium tuber-culosis among children in China. Tuberculosis (Edinb). 2015;95(3):315-320. https://doi.org/10.1016/j.tube.2015.02.041
3. Navarro P. D., Almeida I. N., Kritski A. L., Ceccato M. D., Maciel M. M. [et al.]. Prevalence of latent Mycobacterium tuberculosis infection in prisoners. J. Bras. Pneumol. 2016;42(5):348-355. https://doi.org/10.1590/S1806-37562016000000001
4. Rao M., Ippolito G., Mfinanga S., Ntoumi F., Yeboah-Manu D. [et al.]. Latent TB Infection (LTBI) – Mycobacterium tuberculosis pathogenesis and the dynamics of the granuloma battleground. Int. J. Infect. Dis. 2019;80:58-61. https://doi.org/10.1016/j.ijid.2019.02.035
5. Tamburini B., Badami G. D., Azgomi M. S., Dieli F., La Manna M. P., Caccamo N. Role of hematopoietic cells in Mycobacterium tuberculosis infection. Tuberculosis (Edinb). 2021;130:102-109. https://doi.org/10.1016/j.tube.2021.102109
6. Lombard R., Doz E., Carreras F., Epardaud M., Le Vern Y. [et al.]. IL-17RA in non-hematopoietic cells controls CXCL-1 and 5 critical to rcruit neutrophils to the lung of mycobacteria-infected mice during the adaptive immune response. PLoS One. 2016;11(2):149-455. https://doi.org/10.1371/journal.pone.0149455
7. Nouailles G., Dorhoi A., Koch M., Zerrahn J., Weiner J. [et al.]. CXCL5-secreting pulmonary epithelial cells drive de-structive neutrophilic inflammation in tuberculosis. J. Clin. Invest. 2014;124(3):1268-1282. https://doi.org/10.1172/JCI72030
8. Parker H. A., Forrester L., Kaldor C. D., Dickerhof N., Hampton M. B. Antimicrobial activity of neutrophils against mycobacteria. Front. Immunol. 2021;12:782495. https://doi.org/10.3389/fimmu.2021.782495
9. Mordyk A. V., Zolotov A. N., Novikov D. G., Kirichenko N. A., Pakhtusova P. O., Ptukhin A. O. NETosis-forming ability of neutrophils in patients with limited and disseminated tuberculous lesions. Tuberkuleз i boleзni legkih. – Tuberculosis and Lung Diseases. 2023;101(3):78-86. (In Russ.). https://doi.org/10.58838/2075-1230-2023-101-3-78-86
10. Novikov D. G., Zolotov A. N., Kirichenko N. A., Mordyk A. V. Method for detection of neutrophil extracellular traps in supravital stained blood preparation. Patent for invention № 2768152. Publ. 23.03.2022, Bull. № 9. (In Russ.).
11. Koh H. J., Kim Y. R., Kim J. S., Yun J. S., Kim S. [et al.]. CD82 hypomethylation is essential for tuberculosis pathogenesis via regulation of RUNX1-Rab5/22. Exp. Mol. Med. 2018;50(5):1-15. https://doi.org/10.1038/s12276-018-0091-4
12. Olive A. J., Smith C. M., Kiritsy M. C., Sassetti C. M. The phagocyte oxidasecontrols tolerance to mycobacterium tuberculosis infection. J. Immunol. 2018;201(6):1705-1716. https://doi.org/10.4049/jimmunol.1800202
13. Papayannopoulos V. Neutrophil extracellular traps in immunity and disease. Nat. Rev. Immunol. 2018;18(2):134-147. https://doi.org/10.1038/nri.2017.105
14. Brinkmann V., Reichard U., Goosmann C., Fauler B., Uhlemann Y. [et al.]. Neutrophil extracellular traps kill bacteria. Science. 2004;303:1532-1535.
15. Borkute R. R., Woelke S., Pei G., Dorhoi A. Neutrophils in Tuberculosis: Cell Biology, Cellular Networking and Multitasking in Host Defense. Int. J. Mol. Sci. 2021;22:4801. https://doi.org/10.3390/ijms22094801
16. Nouailles G., Dorhoi A., Koch M., Zerrahn J., Weiner J. [et al.]. CXCL5-secreting pulmonary epithelial cells drive destructive neutrophilic inflammation in tuberculosis. J. Clin. Invest. 2014;124:1268-1282.
17. Corleis B., Dorhoi A. Early dynamics of innate immunity during pulmonary tuberculosis. Immunol. Lett. 2020;221:56-60. https://doi.org/10.1016/j.imlet.2020.02.010
18. Yousefi S., Simon H. U. NETosis – Does it really represent nature’s «Suicide Bomber»? Front. Immunol. 2016;7:328. https://doi.org/10.3389/fimmu.2016.00328

Keywords: Tuberculosis, children, neutrophil extracellular traps, NETosis, neutrophil’s NETs-forming ability


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