<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Allergy</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Allergy</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский Аллергологический Журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1810-8830</issn><issn publication-format="electronic">2686-682X</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">16930</article-id><article-id pub-id-type="doi">10.36691/RJA16930</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Научные обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Immunomodulatory effect of hemozoin from Opisthorchis felineus and its participation in reducing allergic inflammation through activation of the inflammasome</article-title><trans-title-group xml:lang="ru"><trans-title>Иммуномодулирующее действие гемозоина Opisthorchis felineus и его участие в снижении аллергического воспаления через активацию инфламмасомы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-5600-5760</contrib-id><name-alternatives><name xml:lang="en"><surname>Melenteva</surname><given-names>Anasyasiay P.</given-names></name><name xml:lang="ru"><surname>Мелентьева</surname><given-names>Анастасия Павловна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>anastasiaymelenteva@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0008-3948-3608</contrib-id><name-alternatives><name xml:lang="en"><surname>Parshutkina</surname><given-names>Tamara A.</given-names></name><name xml:lang="ru"><surname>Паршуткина</surname><given-names>Тамара Андреевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>tamara.parshutkina@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-2962-1076</contrib-id><name-alternatives><name xml:lang="en"><surname>Ogorodova</surname><given-names>Ludmila M.</given-names></name><name xml:lang="ru"><surname>Огородова</surname><given-names>Людмила Михайловна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Med.), Professor, corresponding member of the Russian Academy of Sciences</p></bio><bio xml:lang="ru"><p>д-р мед. наук, профессор, член-корр. РАН</p></bio><email>edu@tomsk.gov.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7130-9609</contrib-id><contrib-id contrib-id-type="spin">5285-4593</contrib-id><name-alternatives><name xml:lang="en"><surname>Fedorova</surname><given-names>Olga S.</given-names></name><name xml:lang="ru"><surname>Фёдорова</surname><given-names>Ольга Сергеевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>MD, Dr. Sci. (Med.)</p></bio><bio xml:lang="ru"><p>д-р мед. наук</p></bio><email>olga.sergeevna.fedorova@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Siberian State Medical University</institution></aff><aff><institution xml:lang="ru">Сибирский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2024-05-14" publication-format="electronic"><day>14</day><month>05</month><year>2024</year></pub-date><pub-date date-type="pub" iso-8601-date="2024-06-16" publication-format="electronic"><day>16</day><month>06</month><year>2024</year></pub-date><volume>21</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>295</fpage><lpage>304</lpage><history><date date-type="received" iso-8601-date="2024-03-02"><day>02</day><month>03</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-04-03"><day>03</day><month>04</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Pharmarus Print Media</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Фармарус Принт Медиа</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Pharmarus Print Media</copyright-holder><copyright-holder xml:lang="ru">Фармарус Принт Медиа</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/" start_date="2026-06-16"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-nd/4.0/</ali:license_ref></license></permissions><self-uri xlink:href="https://rusalljournal.ru/raj/article/view/16930">https://rusalljournal.ru/raj/article/view/16930</self-uri><abstract xml:lang="en"><p>Molecules of the excretory-secretory product arising as a result of co-evolution of a host and a parasite are able to inhibit the type 2 immune response, while activating the type 1 and the type 17 responses. The ability to alter the immune response can be used to inhibit inflammation in allergic diseases. In this regard, a search for helminth-associated molecules both with an immunomodulatory effect and immunogenicity and low toxicity is represented as a topical task.</p> <p>Hemozoin being a dark brown insoluble biocrystal is an excretory product of a number of hematophagous parasites (<italic>Schistosoma mansoni</italic>, <italic>Plasmodium falciparum </italic>and <italic>Opisthorchis felineus</italic>). This substance as a compound of parasitic origin with explicit immunomodulatory properties has prospects for deep research.</p> <p>Lots of relevant literature has been studied carefully before developing a concept about <italic>Opisthorchis felineus </italic>hemozoin and its unique properties.</p> <p>Thus, the current review presents an analysis of the accumulated data regarding the effect of <italic>Opisthorchis felineus </italic>trematode on the host immune system. Also the data on the immunomodulatory effect of hemozoin of various origins is analyzed. The current knowledge on the immune mechanisms of inflammasome activation and the possible role of hemozoin in reducing allergic inflammation through this mechanism is represented in this article.</p> <p>According to the systemized research results the excretory-secretory molecule of the liver fluke is a product of parasitic origin with an explicit immunomodulatory effect which is promising for prospective scientific study. <italic>Opisthorchis felineus </italic>extract increases the expression of T-regulatory cells and inhibits the Th2-immune response.</p> <p>Hemozoin produced by <italic>Opisthorchis felineus</italic>, like one produced by <italic>Plasmodium falciparum</italic>, may be involved in reducing the activity of allergic inflammation through activation of the inflammasome. Comprehension of the mechanism of how hemozoin interacts with the host immune system can be applied for correction of conditions associated with Th2-polarization of the immune response, which primarily include atopic diseases.</p> <p>Studying the mechanism of inflammation will help by the search for a biological target to create a vaccine to prevent the spread of atopic diseases, including bronchial asthma.</p></abstract><trans-abstract xml:lang="ru"><p>Mолекулы экскреторно-секреторного продукта, возникшие в результате совместной эволюции хозяина и паразита, могут подавлять иммунный ответ 2-го типа, и при этом активировать ответы 1-го и 17-го типов. Эту способность изменять иммунный ответ можно использовать для подавления воспаления при аллергических заболеваниях, в связи с чем поиск гельминтассоциированных молекул, обладающих наряду с иммуногенностью и низкой токсичностью иммуномодулирующим действием, представляется актуальной задачей.</p> <p>Гемозоин ― тёмно-коричневый нерастворимый биокристалл, экскреторный продукт ряда гематофаговых паразитов (<italic>Schistosoma mansoni</italic>, <italic>Plasmodium falciparum </italic>и <italic>Opisthorchis felineus</italic>). Данное вещество является перспективным для изучения соединением паразитарного происхождения, обладает выраженными иммуномодулирующими свойствами. Для формирования представления о гемозоине <italic>Opisthorchis felineus</italic> и его свойствах требуется тщательное изучение литературы.</p> <p>В настоящем обзоре представлен анализ накопленных данных в отношении влияния трематоды <italic>Opisthorchis felineus </italic>на иммунную систему хозяина. Проанализированы данные об иммуномодулирующем действии гемозоина различного происхождения. Представлены современные сведения об иммунных механизмах активации инфламмасомы и возможной роли гемозоина в уменьшении аллергического воспаления посредством данного механизма.</p> <p>Согласно результатам исследований, систематизированным в данной статье, экскреторно-секреторная молекула печёночной двуустки является перспективным для будущих исследований продуктом паразитарного происхождения с выраженным иммуномодулирующим действием. Экстракт <italic>Opisthorchis felineus </italic>увеличивает экспрессию Т-регуляторных клеток и подавляет Th2-иммунный ответ.</p> <p>Гемозоин <italic>Opisthorchis felineus</italic>, как и гемозоин <italic>Plasmodium falciparum</italic>, может принимать участие в уменьшении активности аллергического воспаления через активацию инфламмасомы. Понимание того, как гемозоин взаимодействует с иммунной системой хозяина, может быть использовано для коррекции состояний, ассоциированных с Th2-поляризацией иммунного ответа, к которым в первую очередь относятся атопические заболевания.</p> <p>Изучение механизмов воспаления поможет в поиске биологической мишени с целью создания вакцины для предотвращения распространённости атопических заболеваний, в том числе бронхиальной астмы.</p></trans-abstract><kwd-group xml:lang="en"><kwd>helminthic invasions</kwd><kwd>opisthorchiasis</kwd><kwd>bronchial asthma</kwd><kwd>cytokines</kwd><kwd>immunomodulation</kwd><kwd>inflammasome</kwd><kwd>hemozoin</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>гельминтные инвазии</kwd><kwd>описторхоз</kwd><kwd>бронхиальная астма</kwd><kwd>цитокины</kwd><kwd>иммуномодуляция</kwd><kwd>инфламмасома</kwd><kwd>гемозоин</kwd></kwd-group><funding-group><funding-statement xml:lang="en">This article was supported by the Research Foundation Flanders (grant № 23-25-00432).</funding-statement><funding-statement xml:lang="ru">Поисково-аналитическая работа выполнена за счёт гранта Российского научного фонда (№ 23-25-00432).</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Vasileiadou S, Ekerljung L, Bjerg A, Goksör E. Asthma increased in young adults from 2008–2016 despite stable allergic rhinitis and reduced smoking. PLoS One. 2021;16(6):e0253322. EDN: VTRWEP doi: 10.1371/journal.pone.0253322</mixed-citation><mixed-citation xml:lang="ru">Vasileiadou S., Ekerljung L., Bjerg A., Goksör E. Asthma increased in young adults from 2008–2016 despite stable allergic rhinitis and reduced smoking // PLoS One. 2021. Vol. 16, N 6. P. e0253322. EDN: VTRWEP doi: 10.1371/journal.pone.0253322</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Windsor JW, Kaplan GG. Evolving epidemiology of IBD. Curr Gastroenterol Rep. 2019;21(8):40. EDN: KHUTQP doi: 10.1007/s11894-019-0705-6</mixed-citation><mixed-citation xml:lang="ru">Windsor J.W., Kaplan G.G. Evolving epidemiology of IBD // Curr Gastroenterol Rep. 2019. Vol. 21, N 8. Р. 40. EDN: KHUTQP doi: 10.1007/s11894-019-0705-6</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Biagioni B, Vitiello G, Bormioli S, et al. Migrants and allergy: A new view of the atopic march. Eur Ann Allergy Clin Immunol. 2019;51(3):100–114. doi: 10.23822/EurAnnACI.1764-1489.96</mixed-citation><mixed-citation xml:lang="ru">Biagioni B., Vitiello G., Bormioli S., et al. Migrants and allergy: A new view of the atopic march // Eur Ann Allergy Clin Immunol. 2019. Vol. 51, N 3. P. 100–114. doi: 10.23822/EurAnnACI.1764-1489.96</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Khosravi M, Mirsamadi ES, Mirjalali H, Zali MR. Isolation and functions of extracellular vesicles derived from parasites: The promise of a new era in immunotherapy, vaccination, and diagnosis. Int J Nanomedicine. 2020;(15):2957–2969. EDN: MJUUBP doi: 10.2147/IJN.S250993</mixed-citation><mixed-citation xml:lang="ru">Khosravi M., Mirsamadi E.S., Mirjalali H., Zali M.R. Isolation and functions of extracellular vesicles derived from parasites: The promise of a new era in immunotherapy, vaccination, and diagnosis // Int J Nanomedicine. 2020. N 15. Р. 2957–2969. EDN: MJUUBP doi: 10.2147/IJN.S250993</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Lothstein KE, Gause WC. Mining helminths for novel therapeutics. Trends Mol Med. 2021;27(4):345–364. doi: 10.1016/j.molmed.2020.12.010</mixed-citation><mixed-citation xml:lang="ru">Lothstein K.E., Gause W.C. Mining helminths for novel therapeutics // Trends Mol Med. 2021. Vol. 27, N 4. Р. 345–364. doi: 10.1016/j.molmed.2020.12.010</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Wenjie S, Ning X, Xuelin W, et al. Helminth therapy for immune-mediated inflammatory diseases: Current and future perspectives. J Inflammat Res. 2022;(15):475–491. EDN: HLEQUG doi: 10.2147/JIR.S348079</mixed-citation><mixed-citation xml:lang="ru">Wenjie S., Ning X., Xuelin W., et al. Helminth therapy for immune-mediated inflammatory diseases: Current and future perspectives // J Inflammat Res. 2022. N 15. Р. 475–491. EDN: HLEQUG doi: 10.2147/JIR.S348079</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Hendrik JP, van der Zande, Zawistowska-Deniziak A, Guigas B. Immune regulation of metabolic homeostasis by helminths and their molecules. Trends Parasitol. 2019;35(10):795–808. doi: 10.1016/j.pt.2019.07.014</mixed-citation><mixed-citation xml:lang="ru">Hendrik J.P., van der Zande., Zawistowska-Deniziak A., Guigas B. Immune regulation of metabolic homeostasis by helminths and their molecules // Trends Parasitol. 2019. Vol. 35, N 10. Р. 795–808. doi: 10.1016/j.pt.2019.07.014</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Wu Z, Wang L, Tang Y, Sun X. Parasite-derived proteins for the treatment of allergies and autoimmune diseases. Front Microbiol. 2017;(8):2164. doi: 10.3389/fmicb.2017.02164</mixed-citation><mixed-citation xml:lang="ru">Wu Z., Wang L., Tang Y., Sun X. Parasite-derived proteins for the treatment of allergies and autoimmune diseases // Front Microbiol. 2017. N 8. Р. 2164. doi: 10.3389/fmicb.2017.02164</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Maruszewska-Cheruiyot M, Szewczak L, Krawczak-Wójcik K, et al. The production of excretory-secretory molecules from Heligmosomoides polygyrus bakeri fourth stage larvae varies between mixed and single sex cultures. Parasit Vectors. 2021;14(1):1–10. EDN: NOZQIY doi: 10.1186/s13071-021-04613-9</mixed-citation><mixed-citation xml:lang="ru">Maruszewska-Cheruiyot M., Szewczak L., Krawczak-Wójcik K., et al. The production of excretory-secretory molecules from Heligmosomoides polygyrus bakeri fourth stage larvae varies between mixed and single sex cultures // Parasit Vectors. 2021. Vol. 14, N 1. Р. 1–10. EDN: NOZQIY doi: 10.1186/s13071-021-04613-9</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Zakeri A, Hansen EP, Andersen SD, et al. Immunomodulation by helminths: Intracellular pathways and extracellular vesicles. Front Immunol. 2018;(9):2349. doi: 10.3389/fimmu.2018.02349</mixed-citation><mixed-citation xml:lang="ru">Zakeri A., Hansen E.P., Andersen S.D., et al. Immunomodulation by helminths: Intracellular pathways and extracellular vesicles // Front Immunol 2018. N 9. Р. 2349. doi: 10.3389/fimmu.2018.02349</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Pershina AG, Saltykova IV, Ivanov VV, et al. Hemozoin "knobs" in O. felineus infected liver. Parasit Vectors. 2015;(8):459. EDN: UZZGJT doi: 10.1186/s13071-015-1061-5</mixed-citation><mixed-citation xml:lang="ru">Pershina A.G., Saltykova I.V., Ivanov V.V., et al. Hemozoin "knobs" in O. felineus infected liver // Parasit Vectors. 2015. N 8. Р. 459. EDN: UZZGJT doi: 10.1186/s13071-015-1061-5</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Lvova M, Zhukova M, Kiseleva E, et al. Hemozoin is a product of heme detoxification in the gut of the most medically important species of the family Opisthorchiidae. Int J Parasitol. 2016;46(3):147–156. doi: 10.1016/j.ijpara.2015.12.003</mixed-citation><mixed-citation xml:lang="ru">Lvova M., Zhukova M., Kiseleva E., et al. Hemozoin is a product of heme detoxification in the gut of the most medically important species of the family Opisthorchiidae // Int J Parasitol. 2016. Vol. 46, N 3. Р. 147–156. doi: 10.1016/j.ijpara.2015.12.003</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Evdoklmova ТА, Ogorodova LM. Influence of chronic opistorchis invasion upon immune response and clinical presentations of pediatric bronchial asthma. Pediatriya: zhurnal imeni G.N. Speranskogo. 2005;84(6):12–17. EDN: HSTFKZ</mixed-citation><mixed-citation xml:lang="ru">Евдокимова Т.А., Огородова Л.М. Влияние хронической описторхозной инвазии на клиническое течение и иммунный ответ при атопической бронхиальной астме у детей // Педиатрия. Журнал им. Г.Н. Сперанского. 2005. Т. 84, № 6. С. 12–17. EDN: HSTFKZ</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Ogorodova LM, Freidin MB, Sazonov AE, et al. Opistorchis felineus invasion influence on immunity in bronchial asthma. Bulletin Siberian Med. 2010;9(3):85–90. EDN: MSMIQD doi: 10.20538/1682-0363-2010-3-85-90.</mixed-citation><mixed-citation xml:lang="ru">Огородова Л.М., Фрейдин М.Б., Сазонов А.Э., и др. Влияние инвазии Opistorchis felineus на иммунный ответ при бронхиальной астме // Бюллетень сибирской медицины. 2010. Т. 9, № 3. С. 85–90. EDN: MSMIQD doi: 10.20538/1682-0363-2010-3-85-90</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Saltykova IV, Ittiprasert W, Nevskaya KV, et al. Hemozoin from the liver fluke, O. felineus, modulates dendritic cell responses in bronchial asthma patients. Front Vet Sci. 2019;(6):332. EDN: PDCHOC doi: 10.3389/fvets.2019.00332</mixed-citation><mixed-citation xml:lang="ru">Saltykova I.V., Ittiprasert W., Nevskaya K.V., et al. Hemozoin from the liver fluke, O. felineus, modulates dendritic cell responses in bronchial asthma patients // Front Vet Sci. 2019. N 6. Р. 332. EDN: PDCHOC doi: 10.3389/fvets.2019.00332</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Ogorodova LM, Freidin MB, Sazonov AE, et al. Study of occurrence and correlation between allergic diseases and opisthorchiasis in the population of the Tomsk Region. Bulletin Siberian Med. 2006;5(4):48–51. EDN: HVQRGH doi: 10.20538/1682-0363-2006-4-48-51</mixed-citation><mixed-citation xml:lang="ru">Огородова Л.М., Фрейдин М.Б., Сазонов А.Э., и др. Изучение распространенности аллергической патологии и описторхозной инвазии и их взаимосвязи у населения Томской области // Бюллетень сибирской медицины. 2006. Т. 5, № 4. С. 48–51. EDN: HVQRGH doi: 10.20538/1682-0363-2006-4-48-51</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Ogorodova LM, Freidin MB, Sazonov AE, et al. A pilot screening of prevalence of atopic states and opisthorchosis and their relationship in people of Tomsk Oblast. Parasitol Res. 2007;101(4):1165–1168. doi: 10.1007/s00436-007-0588-6</mixed-citation><mixed-citation xml:lang="ru">Ogorodova L.M., Freidin M.B., Sazonov A.E., et al. A pilot screening of prevalence of atopic states and opisthorchosis and their relationship in people of Tomsk Oblast // Parasitol Res. 2007. Vol. 101, N 4. Р. 1165–1168. doi: 10.1007/s00436-007-0588-6</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Fedorova OS, Janse JJ, Ogorodova LM, et al. O. felineus negatively associates with skin test reactivity in Russia-EuroPrevall-International Cooperation study. Allergy. 2017;72(7):1096–1104. EDN: XMXPYP doi: 10.1111/all.13120</mixed-citation><mixed-citation xml:lang="ru">Fedorova O.S., Janse J.J., Ogorodova L.M., et al. O. felineus negatively associates with skin test reactivity in Russia-EuroPrevall-International Cooperation study // Allergy. 2017. Vol. 72, N 7. Р. 1096–1104. EDN: XMXPYP doi: 10.1111/all.13120</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Fyodorova OS. Food allergy prevalence in children of opisthorchiasis world region. Bulletin Siberian Med. 2010;9(5):102–107. EDN: MVJFYX doi: 10.20538/1682-0363-2010-5-102-107</mixed-citation><mixed-citation xml:lang="ru">Фёдорова О.С. Распространенность пищевой аллергии у детей в мировом очаге описторхоза // Бюллетень сибирской медицины. 2010. Т. 9, № 5. С. 102–107. EDN: MVJFYX doi: 10.20538/1682-0363-2010-5-102-107</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Saltykova IV, Ogorodova LM, Bragina EY, et al. O. felineus liver fluke invasion is an environmental factor modifying genetic risk of atopic bronchial asthma. Acta Trop. 2014;(139):53–56. EDN: UEMZWL doi: 10.1016/j.actatropica.2014.07.004</mixed-citation><mixed-citation xml:lang="ru">Saltykova I.V., Ogorodova L.M., Bragina E.Y., et al. O. felineus liver fluke invasion is an environmental factor modifying genetic risk of atopic bronchial asthma // Acta Trop. 2014. N 139. Р. 53–56. EDN: UEMZWL doi: 10.1016/j.actatropica.2014.07.004</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Kirillova NA, Deyev IA, Kremer YE, et al. T-regulatory cells subpopulation in bronchial asthma and heterogeneous phenotypes of chronic obstructive pulmonary disease. Bulletin Siberian Med. 2011;10(1):48–54. EDN: MKRKHY doi: 10.20538/1682-0363-2011-1-48-54</mixed-citation><mixed-citation xml:lang="ru">Кириллова Н.А., Деев И.А., Кремер Е.Э., и др. Субпопуляции Т-регуляторных клеток при бронхиальной астме и гетерогенных фенотипах хронической обструктивной болезни легких // Бюллетень сибирской медицины. 2011. Т. 10, № 1. С. 48–54. EDN: MKRKHY doi: 10.20538/1682-0363-2011-1-48-54</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Gonsorunova DS, Ogorodova LM, Fyodorova OS, et al. Т-regulatory cells in atopic dermatitis immune response. Bulletin Siberian Med. 2011;10(4):82–88. EDN: OFNNVD doi: 10.20538/1682-0363-2011-4-82-88</mixed-citation><mixed-citation xml:lang="ru">Гонсорунова Д.С., Огородова Л.М., Фёдорова О.С., и др. Участие Т-регуляторных клеток в иммунном ответе при атопическом дерматите // Бюллетень сибирской медицины. 2011. Т. 10, № 4. С. 82–88. EDN: OFNNVD doi: 10.20538/1682-0363-2011-4-82-88</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Kremer EÉ, Ogorodova LM, Kirillova NA, et al. [Immunophenotypic characteristic of dendritic cells in bronchial asthma in conditions of extract O. felineus in vitro. (In Russ)]. Annals Russ Academ Med Sci. 2013;(5):66–70. EDN: QCUWIL doi: 10.15690/vramn.v68i5.665</mixed-citation><mixed-citation xml:lang="ru">Kremer E.E., Ogorodova L.M., Kirillova N.A., et al. [Immunophenotypic characteristic of dendritic cells in bronchial asthma in conditions of extract O. felineus in vitro. (In Russ)] // Annals Russ Academ Med Sci. 2013. N 5. Р. 66–70. EDN: QCUWIL doi: 10.15690/vramn.v68i5.665</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Pack AD, Schwartzhoff PV, Zacharias ZR, et al. Hemozoin-mediated inflammasome activation limits long-lived anti-malarial immunity. Cell Rep. 2021;36(8):109586. doi: 10.1016/j.celrep.2021.109586</mixed-citation><mixed-citation xml:lang="ru">Pack A.D., Schwartzhoff P.V., Zacharias Z.R., et al. Hemozoin-mediated inflammasome activation limits long-lived anti-malarial immunity // Cell Rep. 2021. Vol. 36, N 8. Р. 109586. doi: 10.1016/j.celrep.2021.109586</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Fontana MF, Saphire EO, Pepper M. Plasmodium infection disrupts the T follicular helper cell response to heterologous immunization. Elife. 2023(12):e83330. doi: 10.7554/eLife.83330</mixed-citation><mixed-citation xml:lang="ru">Fontana M.F., Saphire E.O., Pepper M. Plasmodium infection disrupts the T follicular helper cell response to heterologous immunization // Elife. 2023. N 12. Р. e83330. doi: 10.7554/eLife.83330</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Surette FA, Guthmiller JJ, Li L, et al. Extrafollicular CD4 T cell-derived IL-10 functions rapidly and transiently to support anti-Plasmodium humoral immunity. PLoS Pathog. 2021;17(2):e1009288. doi: 10.1371/journal.ppat.1009288</mixed-citation><mixed-citation xml:lang="ru">Surette F.A., Guthmiller J.J., Li L., et al. Extrafollicular CD4 T cell-derived IL-10 functions rapidly and transiently to support anti-Plasmodium humoral immunity // PLoS Pathog. 2021. Vol. 17, N 2. Р. e1009288. doi: 10.1371/journal.ppat.1009288</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Chen MM, Shi L, Sullivan DJ. Haemoproteus and schistosoma synthesize heme polymers similar to plasmodium hemozoin and beta-hematin. Mol Biochem Parasitol. 2001;113(1):1–8. doi: 10.1016/s0166-6851(00)00365-0</mixed-citation><mixed-citation xml:lang="ru">Chen M.M., Shi L., Sullivan D.J. Haemoproteus and schistosoma synthesize heme polymers similar to plasmodium hemozoin and beta-hematin // Mol Biochem Parasitol. 2001. Vol. 113, N 1. Р. 1–8. doi: 10.1016/s0166-6851(00)00365-0</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Hoang AN, Ncokazi KK, de Villiers KA, et al. Crystallization of synthetic haemozoin (beta-haematin) nucleated at the surface of lipid particles. Dalton Trans. 2010;39(5):1235–1244. doi: 10.1039/b914359a</mixed-citation><mixed-citation xml:lang="ru">Hoang A.N., Ncokazi K.K., de Villiers K.A., et al. Crystallization of synthetic haemozoin (beta-haematin) nucleated at the surface of lipid particles // Dalton Trans. 2010. Vol. 39, N 5. Р. 1235–1244. doi: 10.1039/b914359a</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Coronado LM, Nadovich CT, Spadafora C. Malarial hemozoin: From target to tool. Biochim Biophys Acta. 2014;1840(6):2032–2041. doi: 10.1016/j.bbagen.2014.02.009</mixed-citation><mixed-citation xml:lang="ru">Coronado L.M., Nadovich C.T., Spadafora C. Malarial hemozoin: From target to tool // Biochim Biophys Acta. 2014. Vol. 1840, N 6. Р. 2032–2041. doi: 10.1016/j.bbagen.2014.02.009</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Xiao SH, Sun J. Schistosoma hemozoin and its possible roles. Int J Parasitol. 2017;47(4):171–183. doi: 10.1016/j.ijpara.2016.10.005</mixed-citation><mixed-citation xml:lang="ru">Xiao S.H., Sun J. Schistosoma hemozoin and its possible roles // Int J Parasitol. 2017. Vol. 47, N 4. Р. 171–183. doi: 10.1016/j.ijpara.2016.10.005</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Egan TJ. Haemozoin formation. Mol Biochem Parasitol. 2008;157(2):127–36. doi: 10.1016/j.molbiopara.2007.11.005</mixed-citation><mixed-citation xml:lang="ru">Egan T.J. Haemozoin formation // Mol Biochem Parasitol. 2008. Vol. 157, N 2. Р. 127–136. doi: 10.1016/j.molbiopara.2007.11.005</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Dostert C, Guarda G, Romero JF, et al. Malarial hemozoin is a Nalp3 inflammasome activating danger signal. PLoS One. 2009;4(8):e6510. doi: 10.1371/journal.pone.0006510</mixed-citation><mixed-citation xml:lang="ru">Dostert C., Guarda G., Romero J.F., et al. Malarial hemozoin is a Nalp3 inflammasome activating danger signal // PLoS One. 2009. Vol. 4, N 8. Р. e6510. doi: 10.1371/journal.pone.0006510</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Uraki R, Das SC, Hatta M, et al. Hemozoin as a novel adjuvant for inactivated whole virion influenza vaccine. Vaccine. 2014;32(41):5295–5300. doi: 10.1016/j.vaccine.2014.07.079</mixed-citation><mixed-citation xml:lang="ru">Uraki R., Das S.C., Hatta M., et al. Hemozoin as a novel adjuvant for inactivated whole virion influenza vaccine // Vaccine. 2014. Vol. 32, N 41. Р. 5295–5300. doi: 10.1016/j.vaccine.2014.07.079</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Griffith JW, Sun T, McIntosh MT, Bucala R. Pure Hemozoin is inflammatory in vivo and activates the NALP3 inflammasome via release of uric acid. J Immunol. 2009;183(8):5208–5220. doi: 10.4049/jimmunol.0713552</mixed-citation><mixed-citation xml:lang="ru">Griffith J.W., Sun T., McIntosh M.T., Bucala R. Pure hemozoin is inflammatory in vivo and activates the NALP3 inflammasome via release of uric acid // J Immunol. 2009. Vol. 183, N 8. Р. 5208–5220. doi: 10.4049/jimmunol.0713552</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Jaramillo M, Gowda DC, Radzioch D, Olivier M. Hemozoin increases IFN-gamma-inducible macrophage nitric oxide generation through extracellular signal-regulated kinase- and NF-kappa B-dependent pathways. J Immunol. 2003;171(8):4243–4253. doi: 10.4049/jimmunol.171.8.4243</mixed-citation><mixed-citation xml:lang="ru">Jaramillo M., Gowda D.C., Radzioch D., Olivier M. Hemozoin increases IFN-gamma-inducible macrophage nitric oxide generation through extracellular signal-regulated kinase- and NF-kappa B-dependent pathways // J Immunol. 2003. Vol. 171, N 8. Р. 4243–4253. doi: 10.4049/jimmunol.171.8.4243</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Urban BC, Todryk S. Malaria pigment paralyzes dendritic cells. J Biol. 2006;5(2):4. doi: 10.1186/jbiol37</mixed-citation><mixed-citation xml:lang="ru">Urban B.C., Todryk S. Malaria pigment paralyzes dendritic cells // J Biol. 2006. Vol. 5, N 2. Р. 4. doi: 10.1186/jbiol37</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Jiang Y, Xue X, Chen X, et al. Hemozoin from Schistosoma japonicum does not affect murine myeloid dendritic cell function. Parasitol Res. 2010;106(3):653–659. doi: 10.1007/s00436-009-1717-1</mixed-citation><mixed-citation xml:lang="ru">Jiang Y., Xue X., Chen X., et al. Hemozoin from Schistosoma japonicum does not affect murine myeloid dendritic cell function // Parasitol Res. 2010. Vol. 106, N 3. Р. 653–659. doi: 10.1007/s00436-009-1717-1</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Truscott M, Evans DA, Gunn M, Hoffmann KF. Schistosoma mansoni hemozoin modulates alternative activation of macrophages via specific suppression of retnla expression and secretion. Infect Immun. 2013;81(1):133–142. doi: 10.1128/IAI.00701-12</mixed-citation><mixed-citation xml:lang="ru">Truscott M., Evans D.A., Gunn M., Hoffmann K.F. Schistosoma mansoni hemozoin modulates alternative activation of macrophages via specific suppression of retnla expression and secretion // Infect Immun. 2013. Vol. 81, N 1. Р. 133–142. doi: 10.1128/IAI.00701-12</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Lee MS, Igari Y, Tsukui T, et al. Current status of synthetic hemozoin adjuvant: A preliminary safety evaluation. Vaccine. 2016;34(18):2055–2061. doi: 10.1016/j.vaccine.2016.02.064</mixed-citation><mixed-citation xml:lang="ru">Lee M.S., Igari Y., Tsukui T., et al. Current status of synthetic hemozoin adjuvant: A preliminary safety evaluation // Vaccine. 2016. Vol. 34, N 18. Р. 2055–2061. doi: 10.1016/j.vaccine.2016.02.064</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Bobade D, Khandare AV, Deval M, et al. Hemozoin-induced activation of human monocytes toward M2-like phenotype is partially reversed by antimalarial drugs-chloroquine and artemisinin. Microbiologyopen. 2019;8(3):e00651. doi: 10.1002/mbo3.651.</mixed-citation><mixed-citation xml:lang="ru">Bobade D., Khandare A.V., Deval M., et al. Hemozoin-induced activation of human monocytes toward M2-like phenotype is partially reversed by antimalarial drugs-chloroquine and artemisinin // Microbiologyopen. 2019. Vol. 8, N 3. Р. e00651. doi: 10.1002/mbo3.651</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Maknitikul S, Luplertlop N, Chaisri U, et al. Featured article: Immunomodulatory effect of hemozoin on pneumocyte apoptosis via CARD9 pathway, a possibly retarding pulmonary resolution. Exp Biol Med (Maywood). 2018;243(5):395–407. doi: 10.1177/1535370218757458</mixed-citation><mixed-citation xml:lang="ru">Maknitikul S., Luplertlop N., Chaisri U., et al. Featured article: Immunomodulatory effect of hemozoin on pneumocyte apoptosis via CARD9 pathway, a possibly retarding pulmonary resolution // Exp Biol Med (Maywood). 2018. Vol. 243, N 5. Р. 395–407. doi: 10.1177/1535370218757458</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Keller CC, Yamo O, Ouma C, et al. Acquisition of hemozoin by monocytes down-regulates interleukin-12 p40 (IL-12p40) transcripts and circulating IL-12p70 through an IL-10-dependent mechanism: In vivo and in vitro findings in severe malarial anemia. Infect Immun. 2006;74(9):5249–5260. doi: 10.1128/IAI.00843-06</mixed-citation><mixed-citation xml:lang="ru">Keller C.C., Yamo O., Ouma C., et al. Acquisition of hemozoin by monocytes down-regulates interleukin-12 p40 (IL-12p40) transcripts and circulating IL-12p70 through an IL-10-dependent mechanism: In vivo and in vitro findings in severe malarial anemia // Infect Immun. 2006. Vol. 74, N 9. Р. 5249–5260. doi: 10.1128/IAI.00843-06</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Sherry BA, Alava G, Tracey KJ, et al. Malaria-specific metabolite hemozoin mediates the release of several potent endogenous pyrogens (TNF, MIP-1 alpha, and MIP-1 beta) in vitro, and altered thermoregulation in vivo. J Inflamm. 1995;45(2):85–96.</mixed-citation><mixed-citation xml:lang="ru">Sherry B.A., Alava G., Tracey K.J., et al. Malaria-specific metabolite hemozoin mediates the release of several potent endogenous pyrogens (TNF, MIP-1 alpha, and MIP-1 beta) in vitro, and altered thermoregulation in vivo // J Inflamm. 1995. Vol. 45, N 2. Р. 85–96.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Ranjan R, Karpurapu M, Rani A, et al. Hemozoin regulates inos expression by modulating the transcription factor NF-ΚB in macrophages. Biochem Mol Biol J. 2016;2(2):10. doi: 10.21767/2471-8084.100019</mixed-citation><mixed-citation xml:lang="ru">Ranjan R., Karpurapu M., Rani A., et al. Hemozoin regulates inos expression by modulating the transcription factor nf-κb in macrophages // Biochem Mol Biol J. 2016. Vol. 2, N 2. Р. 10. doi: 10.21767/2471-8084.100019</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">Dostert C, Guarda G, Romero JF, et al. Malarial hemozoin is a Nalp3 inflammasome activating danger signal. PLoS One. 2009;4(8):e6510. doi: 10.1371/journal.pone.0006510</mixed-citation><mixed-citation xml:lang="ru">Dostert C., Guarda G., Romero J.F., et al. Malarial hemozoin is a Nalp3 inflammasome activating danger signal // PLoS One. 2009. Vol. 4, N 8. Р. e6510. doi: 10.1371/journal.pone.0006510</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Perkins DJ, Moore JM, Otieno J, et al. In vivo acquisition of hemozoin by placental blood mononuclear cells suppresses PGE2, TNF-alpha, and IL-10. Biochem Biophys Res Commun. 2003;311(4):839–846. doi: 10.1016/j.bbrc.2003.10.073</mixed-citation><mixed-citation xml:lang="ru">Perkins D.J., Moore J.M., Otieno J., et al. In vivo acquisition of hemozoin by placental blood mononuclear cells suppresses PGE2, TNF-alpha, and IL-10 // Biochem Biophys Res Commun. 2003. Vol. 311, N 4. Р. 839–846. doi: 10.1016/j.bbrc.2003.10.073</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">Shio MT, Eisenbarth SC, Savaria M, et al. Malarial hemozoin activates the NLRP3 inflammasome through Lyn and Syk kinases. PLoS Pathog. 2009;5(8):e1000559. doi: 10.1371/journal.ppat.1000559</mixed-citation><mixed-citation xml:lang="ru">Shio M.T., Eisenbarth S.C., Savaria M., et al. Malarial hemozoin activates the NLRP3 inflammasome through Lyn and Syk kinases // PLoS Pathog. 2009. Vol. 5, N 8. Р. e1000559. doi: 10.1371/journal.ppat.1000559</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">Saltykova IV, Ittiprasert W, Nevskaya KV, et al. Hemozoin from the liver fluke, O. felineus, modulates dendritic cell responses in bronchial asthma patients. Front Vet Sci. 2019;(6):332. doi: 10.3389/fvets.2019.00332</mixed-citation><mixed-citation xml:lang="ru">Saltykova I.V., Ittiprasert W., Nevskaya K.V., et al. Hemozoin from the liver fluke, O. felineus, modulates dendritic cell responses in bronchial asthma patients // Front Vet Sci. 2019. N 6. Р. 332. doi: 10.3389/fvets.2019.00332</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">Schwarzer E, Skorokhod OA, Barrera V, Arese P. Hemozoin and the human monocyte: A brief review of their interactions. Parassitologia. 2008;50(1-2):143–145.</mixed-citation><mixed-citation xml:lang="ru">Schwarzer E., Skorokhod O.A., Barrera V., Arese P. Hemozoin and the human monocyte: A brief review of their interactions // Parassitologia. 2008. Vol. 50, N 1-2. Р. 143–145.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Deroost K, Tyberghein A, Lays N, et al. Hemozoin induces lung inflammation and correlates with malaria-associated acute respiratory distress syndrome. Am J Respir Cell Mol Biol. 2013;48(5):589–600. doi: 10.1165/rcmb.2012-0450OC</mixed-citation><mixed-citation xml:lang="ru">Deroost K., Tyberghein A., Lays N., et al. Hemozoin induces lung inflammation and correlates with malaria-associated acute respiratory distress syndrome // Am J Respir Cell Mol Biol. 2013. Vol. 48, N 5. Р. 589–600. doi: 10.1165/rcmb.2012-0450OC</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">Skorokhod OA, Alessio M, Mordmüller B, et al. Hemozoin (malarial pigment) inhibits differentiation and maturation of human monocyte-derived dendritic cells: A peroxisome proliferator-activated receptor-gamma-mediated effect. J Immunol. 2004;173(6):4066–4074. doi: 10.4049/jimmunol.173.6.4066</mixed-citation><mixed-citation xml:lang="ru">Skorokhod O.A., Alessio M., Mordmüller B., et al. Hemozoin (malarial pigment) inhibits differentiation and maturation of human monocyte-derived dendritic cells: A peroxisome proliferator-activated receptor-gamma-mediated effect // J Immunol. 2004. Vol. 173, N 6. Р. 4066–4074. doi: 10.4049/jimmunol.173.6.4066</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">Schwarzer E, Alessio M, Ulliers D, Arese P. Phagocytosis of the malarial pigment, hemozoin, impairs expression of major histocompatibility complex class II antigen, CD54, and CD11c in human monocytes. Infect Immun. 1998;66(4):1601–1606. doi: 10.1128/IAI.66.4.1601-1606.1998</mixed-citation><mixed-citation xml:lang="ru">Schwarzer E., Alessio M., Ulliers D., Arese P. Phagocytosis of the malarial pigment, hemozoin, impairs expression of major histocompatibility complex class II antigen, CD54, and CD11c in human monocytes // Infect Immun. 1998. Vol. 66, N 4. Р. 1601–1606. doi: 10.1128/IAI.66.4.1601-1606.1998</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Waseem S, Ur-Rehman K, Kumar R, Mahmood T. Hemozoin enhances maturation of murine bone marrow derived macrophages and myeloid dendritic cells. Iran J Immunol. 2016;13(1):1–8.</mixed-citation><mixed-citation xml:lang="ru">Waseem S., Ur-Rehman K., Kumar R., Mahmood T. Hemozoin enhances maturation of murine bone marrow derived macrophages and myeloid dendritic cells // Iran J Immunol. 2016. Vol. 13, N 1. Р. 1–8.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">Cambos M, Bazinet S, Abed E, et al. The IL-12p70/IL-10 interplay is differentially regulated by free heme and hemozoin in murine bone-marrow-derived macrophages. Int J Parasitol. 2010;40(9):1003–1012. doi: 10.1016/j.ijpara.2010.02.007</mixed-citation><mixed-citation xml:lang="ru">Cambos M., Bazinet S., Abed E., et al. The IL-12p70/IL-10 interplay is differentially regulated by free heme and hemozoin in murine bone-marrow-derived macrophages // Int J Parasitol. 2010. Vol. 40, N 9. Р. 1003–1012. doi: 10.1016/j.ijpara.2010.02.007</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">Shi W, Xu N, Wang X, et al. Helminth therapy for immune-mediated inflammatory diseases: Current and future perspectives. J Inflamm Res. 2022;(15):475–491. doi: 10.2147/JIR.S348079</mixed-citation><mixed-citation xml:lang="ru">Shi W., Xu N., Wang X., et al. Helminth therapy for immune-mediated inflammatory diseases: Current and future perspectives // J Inflamm Res. 2022. N 15. Р. 475–491. doi: 10.2147/JIR.S348079</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Liu JY, Li LY, Yang XZ, et al. Adoptive transfer of dendritic cells isolated from helminth-infected mice enhanced T regulatory cell responses in airway allergic inflammation. Parasite Immunol. 2011;(33):525–534. doi: 10.1111/j.1365-3024.2011.01308.x</mixed-citation><mixed-citation xml:lang="ru">Liu J.Y., Li L.Y., Yang X.Z., et al. Adoptive transfer of dendritic cells isolated from helminth-infected mice enhanced T regulatory cell responses in airway allergic inflammation // Parasite Immunol. 2011. N 33. Р. 525–534. doi: 10.1111/j.1365-3024.2011.01308.x</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">Coronado LM, Nadovich CT, Spadafora C. Malarial hemozoin: From target to tool. Biochim Biophys Acta. 2014;1840(6):2032–2041. doi: 10.1016/j.bbagen.2014.02.009</mixed-citation><mixed-citation xml:lang="ru">Coronado L.M., Nadovich C.T., Spadafora C. Malarial hemozoin: From target to tool // Biochim Biophys Acta. 2014. Vol. 1840, N 6. Р. 2032–2041. doi: 10.1016/j.bbagen.2014.02.009</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">Broz P, Dixit VM. Inflammasomes: Mechanism of assembly, regulation and signalling. Nat Rev Immunol. 2016;16(7):407–420. doi: 10.1038/nri.2016.58</mixed-citation><mixed-citation xml:lang="ru">Broz P., Dixit V.M. Inflammasomes: Mechanism of assembly, regulation and signalling // Nat Rev Immunol. 2016. Vol. 16, N 7. Р. 407–420. doi: 10.1038/nri.2016.58</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">Toldo S, Mauro AG, Cutter Z, Abbate A. Inflammasome, pyroptosis, and cytokines in myocardial ischemia-reperfusion injury. Am J Physiol Heart Circ Physiol. 2018;315(6):H1553–H1568. doi: 10.1152/ajpheart.00158.2018</mixed-citation><mixed-citation xml:lang="ru">Toldo S., Mauro A.G., Cutter Z., Abbate A. Inflammasome, pyroptosis, and cytokines in myocardial ischemia-reperfusion injury // Am J Physiol Heart Circ Physiol. 2018. Vol. 315, N 6. Р. H1553–H1568. doi: 10.1152/ajpheart.00158.2018</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">De Queiroz GA, da Silva RR, de Pires AO, et al. New variants in NLRP3 inflammasome genes increase risk for asthma and Blomia tropicalis-induced allergy in a Brazilian population. Cytokine X. 2020;2(3):100032. doi: 10.1016/j.cytox.2020.100032</mixed-citation><mixed-citation xml:lang="ru">De Queiroz G.A., da Silva R.R., de Pires A.O., et al. New variants in NLRP3 inflammasome genes increase risk for asthma and blomia tropicalis-induced allergy in a Brazilian population // Cytokine X. 2020. Vol. 2, N 3. Р. 100032. doi: 10.1016/j.cytox.2020.100032</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Madouri F, Guillou N, Fauconnier L, et al. Caspase-1 activation by NLRP3 inflammasome dampens IL-33-dependent house dust mite-induced allergic lung inflammation. J Mol Cell Biol. 2015;7(4):351–365. doi: 10.1093/jmcb/mjv012</mixed-citation><mixed-citation xml:lang="ru">Madouri F., Guillou N., Fauconnier L., et al. Caspase-1 activation by NLRP3 inflammasome dampens IL-33-dependent house dust mite-induced allergic lung inflammation // J Mol Cell Biol. 2015. Vol. 7, N 4. P. 351–365. doi: 10.1093/jmcb/mjv012</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">Préfontaine D, Lajoie-Kadoch S, Foley S, et al. Increased expression of IL-33 in severe asthma: Evidence of expression by airway smooth muscle cells. J Immunol. 2009;183(8):5094–5103. doi: 10.4049/jimmunol.0802387</mixed-citation><mixed-citation xml:lang="ru">Préfontaine D., Lajoie-Kadoch S., Foley S., et al. Increased expression of IL-33 in severe asthma: Evidence of expression by airway smooth muscle cells // J Immunol. 2009. Vol. 183, N 8. Р. 5094–5103. doi: 10.4049/jimmunol.0802387</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">Faustino LD, Griffith JW, Rahimi RA, et al. Luster interleukin-33 activates regulatory T cells to suppress innate γδ T cell responses in the lung. Nat Immunol. 2020;21(11):1371–1383. doi: 10.1038/s41590-020-0785-3</mixed-citation><mixed-citation xml:lang="ru">Faustino L.D., Griffith J.W., Rahimi R.A., et al. Luster interleukin-33 activates regulatory T cells to suppress innate γδ T cell responses in the lung // Nat Immunol. 2020. Vol. 21, N 11. Р. 1371–1383. doi: 10.1038/s41590-020-0785-3</mixed-citation></citation-alternatives></ref></ref-list></back></article>
