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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">medlit</journal-id><journal-title-group><journal-title xml:lang="ru">Гигиена и санитария</journal-title><trans-title-group xml:lang="en"><trans-title>Hygiene and Sanitation</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">0016-9900</issn><issn pub-type="epub">2412-0650</issn><publisher><publisher-name>Federal Scientific Center of Hygiene named after F.F. Erisman</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47470/0016-9900-2025-104-9-1179-1184</article-id><article-id custom-type="edn" pub-id-type="custom">neuxso</article-id><article-id custom-type="elpub" pub-id-type="custom">medlit-5158</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ПРОФИЛАКТИЧЕСКАЯ ТОКСИКОЛОГИЯ И ГИГИЕНИЧЕСКОЕ НОРМИРОВАНИЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PREVENTIVE TOXICOLOGY AND HYGIENIC STANDARTIZATION</subject></subj-group></article-categories><title-group><article-title>Особенности нейроиммунной регуляции у детей с патологией вегетативной нервной системы в условиях хронической аэрогенной экспозиции алюминием</article-title><trans-title-group xml:lang="en"><trans-title>Peculiarities of neuroimmune regulation in children with pathology of the autonomic nervous system under conditions of chronic exposure to airborne aluminum</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2057-9828</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Аликина</surname><given-names>Инга Николаевна</given-names></name><name name-style="western" xml:lang="en"><surname>Alikina</surname><given-names>Inga N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Науч. сотр. отд. иммунобиологических методов диагностики ФБУН ФНЦ МПТ УРЗН Роспотребнадзора, 614045, Пермь, Россия</p><p>e-mail: alikina.in@mail.ru</p></bio><bio xml:lang="en"><p>Researcher, Department of Immunobiological diagnostic methods, Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation</p><p>e-mail: alikina.in@mail.ru</p></bio><email xlink:type="simple">alikina.in@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4860-3145</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Долгих</surname><given-names>Олег Владимирович</given-names></name><name name-style="western" xml:lang="en"><surname>Dolgikh</surname><given-names>Oleg V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Доктор мед. наук, профессор, зав. отд. иммунобиологических методов диагностики ФБУН ФНЦ МПТ УРЗН Роспотребнадзора, 614045, Пермь, Россия</p><p>e-mail: oleg@fcrisk.ru</p></bio><bio xml:lang="en"><p>DSc (Medicine), professor, head, Department of immunobiological diagnostic methods, Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation</p><p>e-mail: oleg@fcrisk.ru</p></bio><email xlink:type="simple">oleg@fcrisk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7166-2448</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ширинкина</surname><given-names>Алиса Сергеевна</given-names></name><name name-style="western" xml:lang="en"><surname>Shirinkina</surname><given-names>Alice S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Науч. сотр. отд. иммунобиологических методов диагностики ФБУН ФНЦ МПТ УРЗН Роспотребнадзора, 614045, Пермь, Россия</p><p>e-mail: shirinkina.ali@yandex.ru</p></bio><bio xml:lang="en"><p>Researcher, Department of immunobiological diagnostic methods, Federal Scientific Center for Medical and Preventive Health Risk Management Technologies, Perm, 614045, Russian Federation</p><p>e-mail: shirinkina.ali@yandex.ru</p></bio><email xlink:type="simple">shirinkina.ali@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФБУН «Федеральный научный центр медико-профилактических технологий управления рисками здоровью населения» Федеральной службы по надзору в сфере защиты прав потребителей и благополучия человека</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal Scientific Center for Medical and Preventive Health Risk Management Technologies</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>21</day><month>10</month><year>2025</year></pub-date><volume>104</volume><issue>9</issue><fpage>1179</fpage><lpage>1184</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Аликина И.Н., Долгих О.В., Ширинкина А.С., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Аликина И.Н., Долгих О.В., Ширинкина А.С.</copyright-holder><copyright-holder xml:lang="en">Alikina I.N., Dolgikh O.V., Shirinkina A.S.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.rjhas.ru/jour/article/view/5158">https://www.rjhas.ru/jour/article/view/5158</self-uri><abstract><sec><title>Введение</title><p>Введение. Алюминий – распространённый экотоксикант, чьё влияние на нейроиммунную регуляцию недостаточно изучено.</p><p>Цель исследования – оценка особенностей изменений специфических показателей нейроиммунной регуляции у детей с патологиями вегетативной нервной системы в условиях хронической низкоуровневой аэрогенной экспозиции алюминием и при наличии полимофизма кандидатных генов.</p></sec><sec><title>Материалы и методы</title><p>Материалы и методы. Обследованы 140 детей, проживающих в условиях влияния выбросов предприятия цветной металлургии (0,1 ПДКс.с.), в том числе 52 ребёнка с расстройствами вегетативной нервной системы (ВНС) и 88 условно здоровых детей. Оценивали экспрессию мембранных рецепторов (Neuropilin-1/CD304, Notch 1) методом проточной цитометрии. Содержание нейротропина-3, серотонина и специфического к алюминию IgG определяли методом иммуноферментного анализа (ИФА). Оценку полиморфизма генов SOD2 (rs2758330) и HTR2A (rs7997012) выполняли методом полимеразной цепной реакции (ПЦР).</p></sec><sec><title>Результаты</title><p>Результаты. Установлено, что у детей с нарушениями ВНС, проживающих в условиях низкоуровневой хронической аэрогенной экспозиции алюминием (0,1 ПДКс.с.), концентрации алюминия в моче (0,011 ± 0,001 мг/дм3) достоверно в 1,7 раза превышали референтные значения (0,0065 ± 0,0035 мг/дм3) и в 2,75 раза (p = 0,0001) значения условно здоровых сверстников (0,004 ± 0,001 мг/дм3). Показано, что у детей основной группы по отношению к группе сравнения наблюдалось угнетение экспрессии NRP1 и Notch 1 (в 2–2,3 раза; p ≤ 0,05), была выражена гиперпродукция нейротропина-3 и специфического к алюминию IgG (в 1,38–1,48 раза; p ≤ 0,05). Установлена тесная корреляционная связь между биоэкспозицией алюминием и гиперпродукцией нейротропина-3 (R2 = 0,86; p ≤ 0,05) и IgG, специфического к алюминию (R2 = 0,52; p ≤ 0,05). Отмечена ассоциация экспрессии гена SOD2 C14510A (аллель A и генотип AA) и гена HTR2A rs7997012 (аллель G и генотип GG) с риском (RR = 1,47–1,56) развития вегетативных расстройств в условиях экспозиции алюминием.</p></sec><sec><title>Ограничения исследования</title><p>Ограничения исследования. Исследование выполнено на ограниченной выборке детей с патологией вегетативной нервной системы (52 ребёнка).</p></sec><sec><title>Заключение</title><p>Заключение. Таким образом, хроническая аэрогенная экспозиция алюминием вызывает дисбаланс нейроиммунной регуляции у детей, что подтверждается исследуемыми маркёрами, перспективными для дальнейших исследований.</p><p>Соблюдение этических стандартов. Исследование проводилось в соответствии с нормами Хельсинкской декларации Всемирной медицинской ассоциации «Этические принципы проведения медицинских исследований с участием людей в качестве субъектов» и Национальным стандартом Российской Федерации ГОСТ Р 52379–2005 «Надлежащая клиническая практика» (ICH E6 GCP) (протокол № 6 от 03.04.2024 г.). Все участники и их законные представители дали информированное добровольное письменное согласие на участие в исследовании.</p></sec><sec><title>Участие авторов</title><p>Участие авторов: Аликина И.Н. – сбор и обработка материала, написание текста, редактирование; Долгих О.В. – проработка концепции и дизайна, написание и редактирование текста, утверждение окончательной версии рукописи; Ширинкина А.С. – сбор и обработка материала, написание текста, редактирование. Все соавторы – ответственность за целостность всех частей статьи.</p></sec><sec><title>Конфликт интересов</title><p>Конфликт интересов. Авторы декларируют отсутствие явных и потенциальных конфликтов интересов в связи с публикацией данной статьи.</p></sec><sec><title>Финансирование</title><p>Финансирование. Исследование не имело спонсорской поддержки.</p></sec><sec><title>Поступила</title><p>Поступила: 18.07.2025 / Принята к печати: .2025 / Опубликована: 20.10.2025</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>Introduction</title><p>Introduction. Aluminum is a common ecotoxicant, whose effect on neuroimmune regulation has not been studied sufficiently. </p><p>The purpose of the study is to assess the changes in specific indicators of neuroimmune regulation in children with autonomic nervous system disorders under conditions of chronic low-level aerogenic exposure to aluminum and in the presence of polymorphisms in candidate genes.</p></sec><sec><title>Materials and methods</title><p>Materials and methods. We examined one hundred forty children exposed to emissions form a non-ferrous metallurgy enterprise (0.1 average daily MPC) including 52 children with disorders of the autonomic nervous system (ANS) (the observation group) and 88 children were considered conditionally healthy (the reference group). The expression of membrane receptors (Neuropilin-1/CD304, Notch 1) was evaluated by flow cytometry. The content of neurotropin-3, serotonin, and specific IgG for aluminum was determined by enzyme immunoassay (ELISA). Evaluation of polymorphism of SOD2 (rs2758330) and HTR2A (rs7997012) genes by using the polymerase chain reaction method (PCR).</p></sec><sec><title>Results</title><p>Results. Children chronically exposed to low-dose airborne aluminum (0.1 average daily MPC) and had ANS disorders were found to have elevated blood aluminum levels (0.011±0.001 mg/dm3). These levels were authentically 1.7 times higher than reference levels (0.0065±0.0035 mg/dm3) and 2.75 times higher (p=0.0001) than aluminum levels identified in their conditionally healthy peers (0.004±0.001 mg/dm3). The children from the observation group were also shown to have inhibited NRP1 and Notch 1 expression compared to the reference group (2.0–2.3 times lower; p≤0.05), as well as hyperproduction of neurotropin-3 and IgG specific to aluminum (1.38–1.48 times higher; p≤0.05). We found a strong correlation between bioexposure to aluminum and hyperproduction of neurotropin-3 (R2=0.86; p≤0.05) and IgG to aluminum (R2=0.52; p≤0.05). As association was established between expression of the SOD2 C14510A gene (allele A and genotype AA) and the HTR2A rs7997012 gene (allele G and genotype GG) and the risk (RR=1.47–1.56) of autonomic nervous system disorders upon exposure to aluminum.</p></sec><sec><title>Limitations</title><p>Limitations. The study was accomplished on a small sample of children (52 cases) with pathology of the autonomic nervous system.</p></sec><sec><title>Conclusion</title><p>Conclusion. Thus, chronic aerogenic exposure to aluminum causes an imbalance of neuroimmune regulation in children, which is confirmed by the studied markers, promising for further research.</p><p>Compliance with ethical standards. The study was conducted in conformity with the Declaration of Helsinki, the World Medical Association “Ethical Principles for Medical Research Involving Human Participants” and the National Standard of the Russian Federation GOST-R 52379–2005 Good Clinical Practice (ICH E6 GCP) (Meeting Report No. 6 dated April 03, 2024). All participants and their legal representatives gave informed voluntary written consent to participate in the study.</p></sec><sec><title>Contributions</title><p>Contributions: Alikina I.N. – data collection and analysis, writing and editing the text; Dolgikh О.V. – study concept and design, writing and editing the text, approval of the final version of the manuscript; Shirinkina А.S. – data collection and analysis, writing and editing the text. All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version</p></sec><sec><title>Conflict of interest</title><p>Conflict of interest. The authors declare no conflict of interest.</p></sec><sec><title>Funding</title><p>Funding. The study had no sponsorship.</p></sec><sec><title>Received</title><p>Received: July 18, 2025 / Accepted: , 2025 / Published: October 20, 2025</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>аэрогенная экспозиция</kwd><kwd>маркёры эффекта и чувствительности</kwd><kwd>алюминий</kwd><kwd>дети</kwd><kwd>ген SOD2 rs2758330</kwd><kwd>ген HTR2A rs7997012</kwd></kwd-group><kwd-group xml:lang="en"><kwd>airborne exposure</kwd><kwd>markers of effect and sensitivity</kwd><kwd>aluminum</kwd><kwd>children</kwd><kwd>SOD2 rs2758330 gene</kwd><kwd>HTR2A rs7997012 gene</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Bondy S.C. Low levels of aluminum can lead to behavioral and morphological changes associated with Alzheimer’s disease and age-related neurodegeneration. 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