Dynamics of the cellular composition of lymphoid nodules in the lungs of guinea pigs sensitized with ovalbumin

Authors

DOI:

https://doi.org/10.26641/2307-0404.2022.3.265741

Keywords:

lymphoid nodule, guinea pig, lung, allergic inflammation, ovalbumin

Abstract

The article discusses the morphological aspects of the dynamics of the cellular composition of lymphoid nodules in the lungs of guinea pigs as a result of an experimental ovalbumin-induced allergic process. We studied the reactivity of immunocompetent cells of lymphoid formations of the lungs after three times subcutaneous sensitization and subsequent 8-day intranasal aeroallergization with ovalbumin in the early and late stage period of the allergic inflammatory process by microscopic, morphometric and statistical methods. By help of morphometric analysis we demonstrate the general regularity of reactivity of a local specific link of the pulmonary immune system to the action of an allergen, which consists in the elevation of the average amount of immune cells of lymphoid nodules of the lungs, starting from the 30th to the 44th day after the start of the experiment. The maximal coefficient of increase by 5.8 times was observed in counting plasma cells among all types of immunocompetent cells of lymphoid nodules in the lungs during the experiment. It has been statistically proven that the implementation of the ovalbumin-induced allergic inflammatory process in the lungs proceeds according to the humoral type and the duration of its course is not limited by the direct influence of the allergen, it also continues after the end of its action, which is a manifestation of changes in compensatory-adaptive processes in the pulmonary immune system with ovalbumin-induced allergic inflammation.

References

Dey P. Basic and Advanced Laboratory Tech-niques in Histopathology and Cytology. Singapore: Springer; 2018. doi: https://www.springer.com/gp/book/9789811082511

Hwang JY, Randall TD, Silva-Sanchez A. Indu-cible Bronchus-Associated Lymphoid Tissue: Taming Inflammation in the Lung. Frontiers in Immunology. 2016 Jun 30;7(258). doi: https://doi.org/10.3389/fimmu.2016.00258

Moro K, Kabata H, Tanabe M, Koga S, Take-no N, Mochizuki M, et al. Interferon and IL-27 antago-nize the function of group 2 innate lymphoid cells and type 2 innate immune responses. Nature Immunology. 2015 Nov 23;17(1):76-86. doi: https://doi.org/10.1038/ni.3309

Lambrecht BN, Hammad H. The immunology of asthma. Nature Immunology. 2014 Dec 18;16(1):45-56. doi: https://doi.org/10.1038/ni.3049

Petrie A, Sabin C. Medical Statistics at a Glance. 4th ed. Wiley-Blackwell; 2019.

Popko SS, Evtushenko VM, Syrtsov VK. In-fluence of pulmonary neuroendocrine cells on lung homeo¬stasis. Zaporozhye medical journal. 2020;22(4):568-75. doi: https://doi.org/10.14739/2310-1210.2020.4.208411

Baluk P, Adams A, Phillips K, Feng J, Hong Y-K, Brown MB, et al. Preferential Lymphatic Growth in Bron-chus-Associated Lymphoid Tissue in Sustained Lung Inflammation. The American Journal of Pathology. 2014 May;184(5):1577-92. doi: https://doi.org/10.1016/j.ajpath.2014.01.021

Klose CSN, Mahlakõiv T, Moeller JB, Rankin LC, Flamar A-L, Kabata H, et al. The neuropeptide neuromedin U stimulates innate lymphoid cells and type 2 inflammation. Nature. 2017;549(7671):282-6. doi: https://doi.org/10.1038/nature23676

Bahriy MM, Dibrova VA, Popadynets' OH, Hry-shchuk MI, Bahriy MM. [Methods of morphological re-search: monograph]. Vinnytsia: Nova knyha; 2016. Ukrainian.

Plas DzhV. [Python for complex tasks. Data Science and Machine Learning]. SPb.: Pyter; 2018. Russian

Published

2022-09-30

How to Cite

1.
 Popko S. Dynamics of the cellular composition of lymphoid nodules in the lungs of guinea pigs sensitized with ovalbumin. Med. perspekt. [Internet]. 2022Sep.30 [cited 2024Apr.28];27(3):16-21. Available from: https://journals.uran.ua/index.php/2307-0404/article/view/265741

Issue

Section

THEORETICAL MEDICINE