Pathogenetic vector of neuroinflammation, psychosomatic concept in asthma in children: prospects for diagnosis and therapy
- Authors: Nesterenko Z.V.1, Ivanina E.Y.2
-
Affiliations:
- Saint Petersburg State Pediatric Medical University
- Gymnasium No. 586 of Vasileostrovsky District
- Issue: Vol 15, No 5 (2024)
- Pages: 57-69
- Section: Reviews
- URL: https://ogarev-online.ru/pediatr/article/view/286933
- DOI: https://doi.org/10.17816/PED15557-69
- ID: 286933
Cite item
Abstract
Asthma incidence is increasing worldwide. Despite significant advances made by world medicine in the diagnosis and treatment of asthma, half of patients receiving standard therapy fail to achieve disease control. As a result of the research, confirmation of the allergic theory of the origin of the disease was found. In 70–80 % of cases, children have an allergic variant of inflammation in asthma. But studies at the micro level cannot explain the causes of the development of chronic inflammation in asthma on a whole-organism scale. The immune system is not autonomous and is regulated by the neuroendocrine system. When analyzing the hormonal status of patients with asthma, a decrease in adaptation to stress was noted. Аsthma is characterized by a state of chronic psycho-emotional stress, the maintenance of which is facilitated by disturbances in neuroendocrine regulation. The psychological component is of great importance in the development of asthma. In this regard, the pharmacological approach alone does not solve problems of a psychological nature; there is a need to use methods of psychological correction for patients with asthma. In addition, a large number of studies have examined the similarities between asthma and epilepsy. The use of anticonvulsants significantly improves the condition of patients with epilepsy and asthma. In severe allergic eosinophilic asthma, it is possible to use the neuroprotector dexpramipexole with the effect of reducing the level of eosinophils and a cortico-sparing effect. Thus, the main cause of asthma development is dysregulation of the neuro-immuno-endocrine system, which results in inflammation and bronchospasm. Considering the importance of regulatory systems in the pathogenesis of asthma, it is advisable to identify the neurophenotype of the disease to increase the effectiveness of treatment and the use of anticonvulsants and psychological correction should be considered in addition to the adopted therapeutic program.
Full Text
##article.viewOnOriginalSite##About the authors
Zoia V. Nesterenko
Saint Petersburg State Pediatric Medical University
Author for correspondence.
Email: zvnesterenk0@gmail.com
ORCID iD: 0000-0001-9522-897X
SPIN-code: 9811-0810
MD, PhD, Dr. Sci. (Medicine), Professor, Department of Propediatrics Сhildhood Diseases
Russian Federation, 2 Litovskaya st., Saint Petersburg, 194100Elena Yu. Ivanina
Gymnasium No. 586 of Vasileostrovsky District
Email: eltaire@gmail.com
ORCID iD: 0009-0003-2489-6606
SPIN-code: 4024-1310
school psychologist
Russian Federation, Saint PetersburgReferences
- b17.ru [Internet]. Volnukhin A.V. Modern neuroscience of bronchial asthma. Available from: https://www.b17.ru (In Russ.)
- Kryzhanovsky GN, editor. Dysregulation pathology. Manual for physicians. Moscow: Meditsina; 2002. 632 p. (In Russ.)
- Ivanova NA, Ryzhov IV, Budzin BB, Nikitina ZS. Increased concentration of kynurenine in serum in children with epilepsy and bronchial asthma. Soviet neurology and psychiatry. 1988;(6):21–24. (In Russ.)
- Kirichenko VI, Lutsenko MT. New investigation methods in neuromorphology. Bulletin physiology and pathology of respiration. 1998;(1):35–45. EDN: HRSCMX
- Interregional public organization Russian Respiratory Society, All-Russian public organization Association of Allergologists and Clinical Immunologists, All-Russian public organization Union of Pediatricians of Russia. Clinical Recommendations of the Russian Federation. Bronchial asthma. Moscow; 2021. 118 p. (In Russ.)
- Kolosov GA, Magsarjav C, Kanesiro KW. Bronchial asthma: a psychosomatic concept in favor of a personalized approach. In: Proceedings of the III International science conferences: “Psychology: traditions and innovations” ; Samara. Samara: LLC “Publishing house ASGARD”; 2018. P. 39–41. (In Russ.)
- National program “Bronchial asthma in children. Treatment strategy and prevention”. 4 th ed., rev. and suppl. Moscow; 2012. 182 p. (In Russ.)
- Yablonsky PK, Polyakova VО, Drobintseva АО, et al. Neuroimmunoendocrinology of the respiratory systemcurrent status of the problem. Progress in physiological science. 2020;51(1):46–57. EDN: MURXHA doi: 10.31857/S0301179820010087
- Alexander F. Psychosomatic medicine it’s principles and applications. New York; 2002. 352 p.
- Balentova S, Conwell S, Myers AC. Neurotransmitters in parasympathetic ganglionic neurons and nerves in mouse lower airway smooth muscle. Respir Physiol Neurobiol. 2013;189(1):195–202. doi: 10.1016/j.resp.2013.07.006
- Barnes PJ. Neural mechanisms in asthma. Br Med Bull. 1992;48 (1):149–168. doi: 10.1093/oxfordjournals.bmb.a072531
- Barrios J, Kho AT, Aven L, et al. Pulmonary neuroendocrine cells secrete gamma-aminobutyric acid to induce goblet cell hyperplasia in primate models. Am J Respir Cell Mol Biol. 2019;60(6):687–694. doi: 10.1165/rcmb.2018-0179OC
- Barrios J, Patel KR, Aven L, et al. Early life allergen-induced mucus overproduction requires augmented neural stimulation of pulmonary neuroendocrine cell secretion. FASEB J. 2017;31(9):4117–4128. doi: 10.1096/fj.201700115R
- Buske-Kirschbaum А, Auer K, Krieger S, Weis Blunted S. Cortisol responses to psychosocial stress in asthmatic children: a general feature of atopic disease? Psychosom Med. 2003;65(5):806–810. doi: 10.1097/01.PSY.0000095916.25975.4F
- Cazzola M, Calzetta L, Matera MG. Long-acting muscarinic antagonists and small airways in asthma: Which link? Allergy. 2021; 76(7):1990–2001. doi: 10.22541/au.160870966.64336849/v
- Cohn L, Elias JA, Chupp GL. Asthma: mechanisms of disease persistence and progression. Annu Rev Immunol. 2004;22:789 –815. doi: 10.1146/annurev.immunol.22.012703.104716
- Cutz E, Pan J, Yeger H, et al. Recent advances and contraversies on the role of pulmonary neuroepithelial bodies as airway sensors. Semin Cell Dev Biol. 2013;24(1):40–50. doi: 10.1016/j.semcdb.2012.09.003
- Davidson RJ, Jackson DC, Kalin NH. Emotion, plasticity, context, and regulation: perspectives from affective neuroscience. Psychol Bull. 2000;126(6):890–909. doi: 10.1037/0033-2909.126.6.890
- Fang L, Sun Q, Roth M. Immunologic and non-immunologic mechanisms leading to airway remodeling in asthma. Int J Mol Sci. 2020;21(3):757. doi: 10.3390/ijms21030757
- Gao R, Peng X, Perry C, et al. Macrophage-derived netrin-1 drives adrenergic nerve-associated lung fibrosis. J Clin Invest. 2021;131(1): e136542. doi: 10.1172/JCI136542
- Hahn C, Islamian AP, Renz H, Nockher WA. Airway epithelial cells produce neurotrophins and promote the survival of eosinophils duri ng allergic airway inflammation. J Allergy Clin Immunol. 2006;117(4):78 7–794. doi: 10.1016/j.jaci.2005.12.133
- Hendifar AE, Marchevsky AM, Tuli R. Neuroendocrine tumors of the lung: current challenges and advances in the diagnosis and management of well-differentiated disease. J Thorac Oncol. 2017;12(3):425–436. doi: 10.1016/j.jtho.2016.11.2222
- Kanda A, Yasutaka Y, Van Bui D, et al. Multiple biological aspects of eosinophils in host defense, eosinophil-associated diseases, immunoregulation, and homeostasis: is their role beneficial, detrimental, regulator or bystander? Biol Pharm Bull. 2020;43(1):20–30. doi: 10.1248/bpb.b19-00892
- Lomia M, Tchelidze T, Pruidze M. Bronchial asthma as neurogenic paroxysmal inflammatory disease: a randomized trial with carbamazepine. Respir. Med. 2006;100(11):1988–1996. doi: 10.1016/j.rmed.2006.02.018
- Mandal J, Roth M, Costa L, et al. Vasoactive intestinal peptide for diagnosing exacerbation in chronic obstructive pulmonary disease. Respiration. 2015;90(5):357–368. doi: 10.1159/000439228
- Minnone G, De Benedetti F, Bracci-Laudiero L. NGF and its receptors in the regulation of inflammatory response. Int J Mol Sci. 2017;18(5):1028. doi: 10.3390/ijms18051028
- Nesterenko ZV, Ivanina YY, Dobrokhotova AV, et al. Allergic diseases in pediatric patients exposed to radiation from the Chernobyl accident and in children born to radiation-exposed parents. European Academy of Allergy and Immunology Congress, 22–26 June 2013. Milan, Italy. P. 1214.
- Pan J, Yeger H, Cutz E. Innervation of pulmonary neuroendocrine cells and neuroepithelial bodies in developing rabbit lung. J Histochem Cytochem. 2004;52(3):379–389. doi: 10.1177/002215540405200309
- Patel KR, Aven L, Shao F, et al. Mast cell-derived neurotrophin 4 mediates allergen-induced airway hyperinnervation in early life. Mucosal Immunol. 2016;9(6):1466–1476. doi: 10.1038/mi.2016.11
- Papi A, Brightling C, Pedersen SE, Reddel HK. Asthma. Lancet. 2018; 391(10122):783–800. doi: 10.1016/S0140-6736(17)33311-1
- Roth M. Airway and lung remodelling in chronic pulmonary obstructive disease: a role for muscarinic receptor antagonists? Drugs. 2015;75:1–8. doi: 10.1007/s40265-014-0319-0
- Rosenkranz MA, Busse WW, Sheridan JF, et al. Are there neurophenotypes for asthma? Functional brain imaging of the interaction between emotion and inflammation in asthma. PLoS One. 2012;7(8): e40921. do i: 10.1371/journal.pone.0040921
- Rudenko М. The role of co-factors in mast cell activation. EMJ Allergy Immunol. 2023;10301305. doi: 10.33590/emjallergyimmunol/10301305
- Ruth P, Cusack RP, Sulaiman I, Gauvreau GM. Refashioning dexpramipexole — a new horizon in eosinophilic asthma? Allergy Clin Immunol. 2023;152(5):1092–1094. doi: 10.1016/j.jaci.2023.09.019
- Schachter SC, Saper CB. Vagus nerve stimulation. Review. Epilepsia. 1998; 39(7):677–686. doi: 10.1111/j.1528-1157.1998.tb01151.x
- Siddiqui S, Wenzel S, Bozik ME, et al. Safety and efficacy of dexpramipexole in eosinophilic asthma (EXHALE) : A randomized controlled trial. J Allergy Clin Immunol. 2023;152(5) :1121–1130. doi: 10.1016/j.jaci.2023.05.014
- Silverman ES, Breault DT, Vallone J, et al. Corticotropin-releasing hormone deficiency allergen-induced airway inflammation in a mouse model of asthma. J Allergy Clin Immunol. 2004;114 (4): 747–754. doi: 10.1016/j.jaci.2004.06.055
- Sun H, Lin A-H, Ru F, et al. KCNQ/M-channels regulate mouse vagal bronchopulmonary c-fiber excitability and cough sensitivity. JCI Insight. 2019;4(5):e124467. doi: 10.1172/jci.insight.124467
- Talbot S, Abdulnour RE, Burkett PR, et al. Silencing nociceptor neurons reduces allergic airway inflammation. Neuron. 2015;87(2):341–354. doi: 10.1016/j.neuron.2015.06.007
- Ural BB, Yeung ST, Damani-Yokota P, et al. Identification of a nerve-associated, lung-resident interstitial macrophage subset with distinct localization and immunoregulatory properties. Sci Immunol. 2020;5(45):eaax8756. doi : 10.1126/sciimmunol.aax8756
- Wenzel SE. Asthma phenotypes: the evolution from clinical to molecular approaches. Nat Med. 2012;18(5):716–725. doi : 10.1038/nm.2678
- Wnuk D, Paw M, Ryczek K, et al. Enhanced asthma-related fibroblast to myofibroblast transition is the result of profibrotic TGF-Beta/Smad2/3 pathway intensification and antifibrotic TGF-β/Smad1/5/(8)9 pathway impairment. Sci Rep. 2020;10:16492. doi: 10.1038/s41598-020-73473-7
- Zhang N, Xu J, Jiang C, Lu S. Neuro-Immune regulation in inflammation and airway remodeling of allergic asthma. Front Immunol. 2022;13:894047. doi: 10.3389/fimmu.2022.894047
Supplementary files
