Markers of allergy and immunoregulation in children under conditions of aerogenic exposure to aluminum
- Authors: Dolgikh O.V.1, Dianova D.G.1, Shirinkina A.S.1
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Affiliations:
- Federal Scientific Center for Medical and Preventive Health Risk Management Technologies
- Issue: Vol 103, No 6 (2024)
- Pages: 591-596
- Section: HYGIENE OF CHILDREN AND ADOLESCENTS
- Published: 25.07.2024
- URL: https://rjsocmed.com/0016-9900/article/view/638199
- DOI: https://doi.org/10.47470/0016-9900-2024-103-6-591-596
- EDN: https://elibrary.ru/puyesv
- ID: 638199
Cite item
Abstract
Introduction. The study of sensitization under conditions of aerogenic exposure to aluminum is relevant for preventing the formation of the risk of disorders of the immunological health in the child population.
Materials and methods. Preschool three hundred fifty three children living in Eastern Siberia were examined. Observation group included 199 children living in the zone exposed to emissions from non-ferrous metallurgy enterprises, comparison group — 154 children living in a “conditionally clean” area. In the observation area, the average daily dose of aerogenic exposure to aluminum was 0.292 ∙ 10–3 mg/(kg ∙ day), in the comparison area — 0.0376 ∙ 10–3mg/(kg ∙ day). The work used sanitary-hygienic, chemical-analytical, enzyme-linked immunosorbent and allergosorbent research methods.
Results. In children living under conditions of aluminum exposure, a twofold excess of aluminum content was identified in biological environments relative to the comparison group (p = 0.001), hyperproduction of IgG to aluminum, CD19+ and CD3+CD8+ lymphocytes (1.6 times), and NKT lymphocytes (2 times) and CD11a+ lymphocytes 1.4 times (p=0.001) was noted, which reflects an imbalance of immunoregulation and the formation of autoallergy. A significant relationship was established between hyperproduction of total IgE and IgG to aluminum (OR=2.29–5.98; 95% CI 1.76–9.52), (RR=1.93–2.66; 95% CI: 1.41–3.54)
Limitations of the study. Limited sample size.
Conclusion. As markers of allergy and imbalance of immunoregulation in children under conditions of aerogenic exposure to aluminum and with its increased content in biological media, it is necessary to recommend IgG to aluminum as a marker of sensitivity, as well as CD11a+, reflecting the likelihood of developing a risk of developing immunological disadaptation and autosensitization (OR = 2.29–5.98), (RR=1.93–2.66).
Compliance with ethical standards. The study design was approved by the Local Ethics Committee of the Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, No. 2 from 03/22/2022.
Contributions:
Dolgikh O.V. — development of the research concept, analysis and interpretation of data, editing of the manuscript;
Dianova D.G. — development of the concept and design of the study, analysis and interpretation of data, writing the manuscript;
Shirinkina A.S. — data collection and processing, tables.
All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version.
Conflict of interest. The authors declare no conflict of interest.
Acknowledgement. The study had no sponsorship.
Received: April 8, 2024 / Accepted: June 19, 2024 / Published: July 17, 2024
Keywords
About the authors
Oleg V. Dolgikh
Federal Scientific Center for Medical and Preventive Health Risk Management Technologies
Author for correspondence.
Email: oleg@fcrisk.ru
ORCID iD: 0000-0003-4860-3145
MD, PhD, DSci., head of the Dept. of immunobiological diagnostic methods of the Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation
e-mail: oleg@fcrisk.ru
Russian FederationDina G. Dianova
Federal Scientific Center for Medical and Preventive Health Risk Management Technologies
Email: dianovadina@rambler.ru
ORCID iD: 0000-0002-0170-1824
MD, PhD, DSci., senior researcher of the Dept. of immunobiological diagnostic methods of the Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation
e-mail: dianovadina@rambler.ru
Russian FederationAlisa S. Shirinkina
Federal Scientific Center for Medical and Preventive Health Risk Management Technologies
Email: shirinkina.ali@yandex.ru
ORCID iD: 0000-0001-7166-2448
Junior researcher of the of the Lab. of immunogenetics of the Dept. of immunobiological diagnostic methods of the Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation
e-mail: shirinkina.ali@yandex.ru
Russian FederationReferences
- State report «On the state of sanitary and epidemiological well-being of the population in the Russian Federation in 2022». Moscow; 2023. (in Russian)
- Efimova N.V., Donskikh I.V., Zarodnyuk T.S., Gornov A.Yu. Assessing and forecasting morbidity of adolescents living in area influenced by aluminium production. Meditsina truda i promyshlennaya ekologiya. 2014; 54(4): 44–9. https://elibrary.ru/scevlx (in Russian)
- Ustinova O.Yu., Valina S.L., Shtina I.E., Kobyakova O.A., Makarova V.G. Features of children’s morbidity living in area of influence enterprises for alumina production. Zdorov’e naseleniya i sreda obitaniya – ZNiSO. 2019; (1): 19–23. https://doi.org/10.35627/2219-5238/2019-310-1-18-23 https://elibrary.ru/fpuhjt (in Russian)
- Skupnevskii S.V., Ivanov D.V. The effect of aluminum and its compounds on the functions of human organs and tissues (review article). Vestnik novykh meditsinskikh tekhnologii. Elektronnoe izdanie. 2023; 17(1): 110–24. https://doi.org/10.24412/2075-4094-2023-1-3-7 https://elibrary.ru/vgrxrm (in Russian)
- Renke G., Almeida V.B.P., Souza E.A., Lessa S., Teixeira R.L., Rocha L., et al. Clinical outcomes of the deleterious effects of aluminum on neuro-cognition, inflammation, and health: A review. Nutrients. 2023; 5(9): 2221. https://doi.org/10.3390/nu15092221
- Kutai V.E., Tsygankov V.Yu. The physicochemical properties and distribution of aluminum in the environment, the effect on living organisms, the reduction of its toxic effect. Meditsinskii akademicheskii zhurnal. 2021; 21(2): 25–36. https://doi.org/10.17816/MAJ64912 https://elibrary.ru/jqstpg (in Russian)
- Zuo Y., Lu X., Wang X., Sooranna S.R., Tao L., Chen S., et al. Correction to: high-dose aluminum exposure further alerts immune phenotype in aplastic anemia patients. Biol. Trace Elem. Res. 2021; 199(8): 3178. https://doi.org/10.1007/s12011-020-02412-4
- Zhang T., He P., Guo D., Chen K., Hu Z., Zou Y. Research progress of aluminum phosphate adjuvants and their action mechanisms. Pharmaceutics. 2023; 15(6): 1756. https://doi.org/10.3390/pharmaceutics15061756.4
- Alasfar R.H., Isaifan R.J. Aluminum environmental pollution: the silent killer. Environ. Sci. Pollut. Res. Int. 2021; 28(33): 44587–97. https://doi.org/10.1007/s11356-021-14700-0
- Hethey C., Hartung N., Wangorsch G., Weisser K., Huisinga W. Physiology-based toxicokinetic modelling of aluminium in rat and man. Arch. Toxicol. 2021; 95(9): 2977–3000. https://doi.org/10.1007/s00204-021-03107-y
- Liao Y., Sun L., Nie M., Li J., Huang X., Heng S., et al. Modulation of skin inflammatory responses by aluminum adjuvant. Pharmaceutics. 2023; 15(2): 576. https://doi.org/10.3390/pharmaceutics15020576
- Linneberg A., Jacobsen R.K., Jespersen L., Abildstrøm S.Z. Association of subcutaneous allergen-specific immunotherapy with incidence of autoimmune disease, ischemic heart disease, and mortality. J. Allergy Clin. Immunol. 2012; 129: 413–9. https://doi.org/10.1016/j.jaci.2011.09.007
- Hoffmann S.S., Thiesson E.M., Johansen J.D., Hviid A. Risk factors for granulomas in children following immunization with aluminium-adsorbed vaccines: A Danish population-based cohort study. Contact. Dermat. 2022; 87: 430–8. https://doi.org/10.1111/cod.14180
- Shugalei I.V., Garabadzhiu A.V., Ilyushin M.A., Sudarikov A.M. Some aspects of the influence of aluminum and its compounds on living organisms. Ekologicheskaya khimiya. 2012; 21(3): 172–86. https://elibrary.ru/stgsyt (in Russian)
- Hethey C., Hartung N., Wangorsch G., Weisser K., Huisinga W. Physiology-based toxicokinetic modelling of aluminium in rat and man. Arch. Toxicol. 2021; 95(9): 2977–3000. https://doi.org/10.1007/s00204-021-03107-y
- Terhune T.D., Deth R.C. Aluminum adjuvant-containing vaccines in the context of the hygiene hypothesis: a risk factor for eosinophilia and allergy in a genetically susceptible subpopulation? Int. J. Environ. Res. Public Health. 2018; 15(5): 901. https://doi.org/10.3390/ijerph15050901
- Zaitseva N.V., Dolgikh O.V., Dianova D.G. Exposure to airborne nickel and phenol and features of the immune response mediated by E and G immunoglobulins. Health Risk Analysis. 2023; (2): 160–8. https://doi.org/10.21668/health.risk/2023.2.16.eng https://elibrary.ru/jqjrso
- Semmes E.C., Chen J.L., Goswami R., Burt T.D., Permar S.R., Fouda G.G. Understanding early-life adaptive immunity to guide interventions for pediatric health. Front. Immunol. 2021; 11: 595297. https://doi.org/10.3389/fimmu.2020.595297
- Kaszubowska L., Foerster J., Kmieć Z. NKT-like (CD3+CD56+) cells differ from T cells in expression level of cellular protective proteins and sensitivity to stimulation in the process of ageing. Immun. Ageing. 2022; 19(1): 18. https://doi.org/10.1186/s12979-022-00274-z
- Mandala W.L. Expression of CD11a, CD11b, CD11c, and CD18 on neutrophils from different clinical types of malaria in Malawian children. J. Blood Med. 2022: 13: 1–10. https://doi.org/10.2147/JBM.S343109
- Hameed M.A., Nafady H.A., Mostafa M.I., Sayed D., Obiedallah A.A. Possible role of CD11a in primary immune thrombocytopenia patients on immunosuppressive therapy. J. Blood Med. 2021; 12: 197–205. https://doi.org/10.2147/JBM.S300717
- Bose T.O., Pham Q.M., Jellison E.R., Mouries J., Ballantyne C.M., Lefrançois L. CD11a regulates effector CD8 T cell differentiation and central memory development in response to infection with Listeria monocytogenes. Infect. Immun. 2013; 81(4): 1140–51. https://doi.org/10.1128/IAI.00749-12
- García-Salido A., Cuenca-Carcelén S., Castillo-Robleda A. CD64, CD11a and CD18 leukocytes expression in children with SARS-CoV-2 multisystem inflammatory syndrome versus children with Kawasaki disease: Similar but not the same. Med. Clin. (Barc). 2021; 156(2): 89–91. https://doi.org/10.1016/j.medcli.2020.09.002
- Costa A.A., Chatterjee J., Cobb O., Sanapala S., Scheaffer S., Guo X., et al. RNA sequence analysis reveals ITGAL/CD11A as a stromal regulator of murine low-grade glioma growth. Neuro-Oncology. 2022; 24(1): 14–26. https://doi.org/10.1093/neuonc/noab130
- Bocharova O.A., Karpova R.V., Bocharov E.V., Vershinskaya A.A., Baryshnikova M.A., Devrishov D.A., et al. Modulation of the adhesion molecules expression on peripheral blood cells in CBA mice during hepatocarcinogenesis. Laboratornye zhivotnye dlya nauchnykh issledovanii. 2020; (1): 42–6. https://doi.org/10.29296/2618723X-2020-01-05 https://elibrary.ru/azwiis (in Russian)
- Wang Y., Shu Y., Xiao Y., Wang Q., Kanekura T., Li Y., et al. Hypomethylation and overexpression of ITGAL (CD11a) in CD4(+) T cells in systemic sclerosis. Clin. Epigenetics. 2014; 6(1): 25. https://doi.org/10.1186/1868-7083-6-25
- Zhu X., Liu B., Ruan Z., Chen M., Li C., Shi H., et al. TMT-based quantitative proteomic analysis reveals downregulation of ITGAL and Syk by the effects of cycloastragenol in OVA-induced asthmatic mice. Oxid. Med. Cell. Longev. 2022; 2022: 6842530. https://doi.org/10.1155/2022/6842530
- Lanin D.V., Zaitseva N.V., Dolgikh O.V. Neuroendocrine mechanisms for regulation of immune system. Uspekhi sovremennoi biologii. 2011; 131(2): 122–34. https://elibrary.ru/ntrviv (in Russian)
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