<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">medsovet</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинский Совет</journal-title><trans-title-group xml:lang="en"><trans-title>Meditsinskiy sovet = Medical Council</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-701X</issn><issn pub-type="epub">2658-5790</issn><publisher><publisher-name>REMEDIUM GROUP Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21518/ms2025-121</article-id><article-id custom-type="elpub" pub-id-type="custom">medsovet-9190</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>ХРОНИЧЕСКИЕ ЗАБОЛЕВАНИЯ ЛЕГКИХ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHRONIC PULMONARY DISEASES</subject></subj-group></article-categories><title-group><article-title>Клинический случай включения тезепелумаба в лечение тяжелой не-Т2 бронхиальной астмы</article-title><trans-title-group xml:lang="en"><trans-title>Clinical case of integrating tezepelumab in the treatment of non-T2 severe bronchial asthma</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9928-926X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гайнитдинова</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Gaynitdinova</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гайнитдинова Вилия Вилевна, д.м.н., профессор кафедры пульмонологии Института клинической медицины имени Н.В. Склифосовского</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Viliya Gaynitdinova, Dr. Sci. (Med.), Professor, Department of Pulmonology, N.V. Sklifosovsky Institute of Clinical Medicine</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">ivv_08@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/0000-0002-3174-5000</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мержоева</surname><given-names>З. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Merzhoeva</surname><given-names>Z. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мержоева Замира Магомедовна, к.м.н., доцент кафедры пульмонологии; заведующая пульмонологическим отделением</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Zamira M. Merzhoeva, Cand. Sci. (Med.), Associate Professor, Pulmonology Department</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">merzhoeva_z_m@staff.sechenov.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/0000-0002-4726-4906</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Нуралиева</surname><given-names>Г. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Nuralieva</surname><given-names>G. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Нуралиева Галия Сериковна, к.м.н., доцент кафедры пульмонологии Института клинической медицины имени Н.В. Склифосовского</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Galiya S. Nuralieva, Cand. Sci. (Med.), Associate Professor, Department of Pulmonology, N.V. Sklifosovsky Institute of Clinical Medicine</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">nuralieva_g@staff.sechenov.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/0009-0004-9275-2601</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соколова</surname><given-names>Е. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Sokolova</surname><given-names>E. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Соколова Елизавета Сергеевна, ординатор кафедры пульмонологии</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Elizaveta S. Sokolova, Resident of the Department of Pulmonology</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">e-li1999@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Богатырева</surname><given-names>Т. У.</given-names></name><name name-style="western" xml:lang="en"><surname>Bogatyreva</surname><given-names>T. U.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Богатырева Тамара Умаровна, аспирант кафедры пульмонологии</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Tamara U. Bogatyreva, Pоstgraduate Student of the Department of Pulmonology</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">toma.bogatyrva.97@inbox.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/0000-0002-1314-0091</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Шмидт</surname><given-names>А. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Shmidt</surname><given-names>A. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Шмидт Анна Евгеньевна, ассистент кафедры пульмонологии</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2</p></bio><bio xml:lang="en"><p>Anna E. Shmidt, Assistant of the Department of Pulmonology </p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991</p></bio><email xlink:type="simple">shmidt_a_e@staff.sechenov.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/0000-0002-5999-2150</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Авдеев</surname><given-names>С. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Avdeev</surname><given-names>S. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Авдеев Сергей Николаевич, д.м.н., профессор, академик РАН, заведующий кафедрой пульмонологии Института клинической медицины имени Н.В. Склифосовского; директор НМИЦ пульмонологии Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет); руководитель клинического отдела, Научно-исследовательский институт пульмонологии Федерального медико-биологического агентства</p><p>119991, Москва, ул. Трубецкая, д. 8, стр. 2,</p><p>115682, Москва, Ореховый бульвар, д. 28</p></bio><bio xml:lang="en"><p>Sergey N. Avdeev, Dr. Sci. (Med.), Professor, Academician of the Russian Academy of Sciences, Head of the Pulmonology Department, N.V. Sklifosovsky Institute of Clinical Medicine; Director of the National Medical Research Center of Pulmonology, Sechenov First Moscow State Medical University (Sechenov University); Head of the Clinical Department, Research Institute for Pulmonology of the Federal Medical Biological Agency</p><p>8, Bldg. 2, Trubetskaya St., Moscow, 119991,</p><p>8, Orekhovy Boulevard, Moscow, 115682</p></bio><email xlink:type="simple">serg_avdeev@list.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Sechenov First Moscow State Medical University (Sechenov University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Первый Московский государственный медицинский университет имени И.М. Сеченова (Сеченовский Университет); &#13;
Научно-исследовательский институт пульмонологии Федерального медико-биологического агентства</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Sechenov First Moscow State Medical University (Sechenov University); &#13;
Research Institute for Pulmonology of the Federal Medical Biological Agency</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2025</year></pub-date><pub-date pub-type="epub"><day>22</day><month>06</month><year>2025</year></pub-date><volume>0</volume><issue>9</issue><fpage>24</fpage><lpage>29</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Гайнитдинова В.В., Мержоева З.М., Нуралиева Г.С., Соколова Е.С., Богатырева Т.У., Шмидт А.Е., Авдеев С.Н., 2025</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="ru">Гайнитдинова В.В., Мержоева З.М., Нуралиева Г.С., Соколова Е.С., Богатырева Т.У., Шмидт А.Е., Авдеев С.Н.</copyright-holder><copyright-holder xml:lang="en">Gaynitdinova V.V., Merzhoeva Z.M., Nuralieva G.S., Sokolova E.S., Bogatyreva T.U., Shmidt A.E., Avdeev S.N.</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.med-sovet.pro/jour/article/view/9190">https://www.med-sovet.pro/jour/article/view/9190</self-uri><abstract><p>Бронхиальная астма (БА) – гетерогенное заболевание, от которого страдают порядка 339 млн человек по всему миру. У большинства пациентов астму можно контролировать с помощью стандартных методов лечения, включая ингаляционные кортикостероиды (ИГКС), бета-агонисты длительного действия (β2-агонисты длительного действия), антихолинергические препараты длительного действия (АХДД) и пероральные антагонисты лейкотриеновых рецепторов. Для более тяжелых случаев, которые остаются неконтролируемыми при стандартном лечении, в настоящее время доступна генно-инженерная биологическая терапия (ГИБТ). Существующие генно-биологические препараты подавляют только определенные молекулярные мишени, такие как IgE и цитокины профиля T-2 воспаления, подходят для небольшой группы пациентов с тяжелой формой астмы и неэффективны при неаллергических или неэозинофильных фенотипах (не Т2) астмы. Однако эти биологические препараты подходят только для группы пациентов с тяжелой Т-2 БА и неэффективны при неаллергических или неэозинофильных фенотипах астмы. Неоднородная реакция на лечение астмы напрямую связана с различиями в характере воспаления дыхательных путей, активации иммунных клеток и чувствительности к глюкокортикоидам. Тезепелумаб – это первое в своем классе моноклональное антитело к тимическому стромальному лимфопоэтину (TSLP), которое назначается при ТБА, независимо от эндотипа воспаления. В представленном клиническом наблюдении включение тезепелумаба в лечение тяжелой неатопической неэозинофильной (не Т-2) неконтролируемой астмы привело к полному контролю симптомов БА, значительному улучшению функции внешнего дыхания и не вызвало нежелательных явлений. Полученные данные совпали с результатами проведенных исследований.</p></abstract><trans-abstract xml:lang="en"><p>Asthma is a heterogeneous disease that affects approximately 339 million people worldwide. In most patients, asthma can be controlled with standard treatments, including inhaled corticosteroids (ICS), long-acting beta-agonists (LABs), long-acting anticholinergics (LACs), and oral leukotriene receptor antagonists. For more severe cases that remain uncontrolled with standard treatment, gene-engineered therapies (GEBTs) are now available. Existing gene-engineered therapies only inhibit specific molecular targets, such as IgE and T-2 inflammatory cytokines, are suitable for a small subset of patients with severe asthma, and are ineffective in non-allergic or non-eosinophilic (non-T2) asthma phenotypes. However, these biological drugs are only suitable for a group of patients with severe T-2 bronchial asthma and are ineffective in non-allergic or non-eosinophilic asthma phenotypes. Heterogeneous response to asthma treatment is directly related to differences in the nature of airway inflammation, immune cell activation, and glucocorticoid sensitivity. Tezepelumab is a first-in-class monoclonal antibody to thymic stromal lymphopoietin (TSLP) that is prescribed for sever asthma, regardless of the endotype of inflammation. In the presented clinical observation, the inclusion of tezepelumab in the treatment of severe non-atopic non-eosinophilic (non-T-2) uncontrolled asthma led to complete control of asthma symptoms, significant improvement in respiratory function, and did not cause adverse events. The data obtained coincided with the results of the studies.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>тимический стромальный лимфопоэтин</kwd><kwd>генно-инженерная биологическая терапия</kwd><kwd>анти-TSLP терапия</kwd><kwd>неконтролируемая астма</kwd><kwd>неэозинофильный эндотип воспаления</kwd></kwd-group><kwd-group xml:lang="en"><kwd>thymic stromal lymphopoietin</kwd><kwd>genetically engineered biological therapy</kwd><kwd>anti-TSLP therapy</kwd><kwd>uncontrolled asthma</kwd><kwd>eosinophilic endotype of inflammation</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">Dharmage SC, Perret JL, Custovic A. Epidemiology of asthma in children and adults. Front Pediatr. 2019;7:246. https://doi.org/10.3389/fped.2019.00246.</mixed-citation><mixed-citation xml:lang="en">Dharmage SC, Perret JL, Custovic A. Epidemiology of asthma in children and adults. Front Pediatr. 2019;7:246. https://doi.org/10.3389/fped.2019.00246.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Trivedi M, Denton E. Asthma in children and adults-what are the differences and what can they tell us about asthma? Front Pediatr. 2019;7:256. https://doi.org/10.3389/fped.2019.00256.</mixed-citation><mixed-citation xml:lang="en">Trivedi M, Denton E. Asthma in children and adults-what are the differences and what can they tell us about asthma? Front Pediatr. 2019;7:256. https://doi.org/10.3389/fped.2019.00256.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Pelaia C, Crimi C, Vatrella A, Tinello C, Terracciano R, Pelaia G. Molecular targets for biological therapies of severe asthma. Front Immunol. 2020;11:603312. https://doi.org/10.3389/fimmu.2020.603312.</mixed-citation><mixed-citation xml:lang="en">Pelaia C, Crimi C, Vatrella A, Tinello C, Terracciano R, Pelaia G. Molecular targets for biological therapies of severe asthma. Front Immunol. 2020;11:603312. https://doi.org/10.3389/fimmu.2020.603312.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Ricciardolo FLM, Bertolini F, Carriero V. The role of dupilumab in severe asthma. Biomedicines. 2021;9(9):1096. https://doi.org/10.3390/biomedicines9091096.</mixed-citation><mixed-citation xml:lang="en">Ricciardolo FLM, Bertolini F, Carriero V. The role of dupilumab in severe asthma. Biomedicines. 2021;9(9):1096. https://doi.org/10.3390/biomedicines9091096.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Eger K, Amelink M, Hashimoto S, Hekking PP, Longo C, Bel EH. Overuse of oral corticosteroids, underuse of inhaled corticosteroids, and implications for biologic therapy in asthma. Respiration. 2022;101(2):116–121. https://doi.org/10.1159/000518514.</mixed-citation><mixed-citation xml:lang="en">Eger K, Amelink M, Hashimoto S, Hekking PP, Longo C, Bel EH. Overuse of oral corticosteroids, underuse of inhaled corticosteroids, and implications for biologic therapy in asthma. Respiration. 2022;101(2):116–121. https://doi.org/10.1159/000518514.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Murdoch JR, Lloyd CM. Chronic inflammation and asthma. Mutat Res. 2010;690(1–2):24–39. https://doi.org/10.1016/j.mrfmmm.2009.09.005.</mixed-citation><mixed-citation xml:lang="en">Murdoch JR, Lloyd CM. Chronic inflammation and asthma. Mutat Res. 2010;690(1–2):24–39. https://doi.org/10.1016/j.mrfmmm.2009.09.005.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Esteban-Gorgojo I, Antolín-Amérigo D, Domínguez-Ortega J, Quirce S. Non-eosinophilic asthma: current perspectives. J Asthma Allergy. 2018;11:267–281. https://doi.org/10.2147/JAA.S153097.</mixed-citation><mixed-citation xml:lang="en">Esteban-Gorgojo I, Antolín-Amérigo D, Domínguez-Ortega J, Quirce S. Non-eosinophilic asthma: current perspectives. J Asthma Allergy. 2018;11:267–281. https://doi.org/10.2147/JAA.S153097.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Menzies-Gow A, Wechsler ME, Brightling CE. Unmet need in severe, uncontrolled asthma: can anti-TSLP therapy with tezepelumab provide a valuable new treatment option? Respir Res. 2020;21(1):268. https://doi.org/10.1186/s12931-020-01505-x.</mixed-citation><mixed-citation xml:lang="en">Menzies-Gow A, Wechsler ME, Brightling CE. Unmet need in severe, uncontrolled asthma: can anti-TSLP therapy with tezepelumab provide a valuable new treatment option? Respir Res. 2020;21(1):268. https://doi.org/10.1186/s12931-020-01505-x.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ziegler SF. Thymic stromal lymphopoietin and allergic disease. J Allergy Clin Immunol. 2012;130(4):845–852. https://doi.org/10.1016/j.jaci.2012.07.010.</mixed-citation><mixed-citation xml:lang="en">Ziegler SF. Thymic stromal lymphopoietin and allergic disease. J Allergy Clin Immunol. 2012;130(4):845–852. https://doi.org/10.1016/j.jaci.2012.07.010.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Gour N, Wills-Karp M. IL-4 and IL-13 signaling in allergic airway disease. Cytokine. 2015;75(1):68–78. https://doi.org/10.1016/j.cyto.2015.05.014.</mixed-citation><mixed-citation xml:lang="en">Gour N, Wills-Karp M. IL-4 and IL-13 signaling in allergic airway disease. Cytokine. 2015;75(1):68–78. https://doi.org/10.1016/j.cyto.2015.05.014.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y, Wang W, Lv Z, Li Y, Chen Y, Huang K et al. Elevated Expression of IL-33 and TSLP in the Airways of Human Asthmatics In Vivo: A Potential Biomarker of Severe Refractory Disease. J Immunol. 2018;200(7):2253–2262. https://doi.org/10.4049/jimmunol.1701455.</mixed-citation><mixed-citation xml:lang="en">Li Y, Wang W, Lv Z, Li Y, Chen Y, Huang K et al. Elevated Expression of IL-33 and TSLP in the Airways of Human Asthmatics In Vivo: A Potential Biomarker of Severe Refractory Disease. J Immunol. 2018;200(7):2253–2262. https://doi.org/10.4049/jimmunol.1701455.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Corren J, Ambrose CS, Sałapa K, Roseti SL, Griffiths JM, Parnes JR, Colice G. Efficacy of Tezepelumab in Patients with Severe, Uncontrolled Asthma and Perennial Allergy. J Allergy Clin Immunol Pract. 2021;9(12):4334–4342.e6. https://doi.org/10.1016/j.jaip.2021.07.045.</mixed-citation><mixed-citation xml:lang="en">Corren J, Ambrose CS, Sałapa K, Roseti SL, Griffiths JM, Parnes JR, Colice G. Efficacy of Tezepelumab in Patients with Severe, Uncontrolled Asthma and Perennial Allergy. J Allergy Clin Immunol Pract. 2021;9(12):4334–4342.e6. https://doi.org/10.1016/j.jaip.2021.07.045.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Corren J, Garcia Gil E, Griffiths JM, Parnes JR, van der Merwe R, Sałapa K, O’Quinn S. Tezepelumab improves patient-reported outcomes in patients with severe, uncontrolled asthma in PATHWAY. Ann Allergy Asthma Immunol. 2021;126(2):187–193. https://doi.org/10.1016/j.anai.2020.10.008.</mixed-citation><mixed-citation xml:lang="en">Corren J, Garcia Gil E, Griffiths JM, Parnes JR, van der Merwe R, Sałapa K, O’Quinn S. Tezepelumab improves patient-reported outcomes in patients with severe, uncontrolled asthma in PATHWAY. Ann Allergy Asthma Immunol. 2021;126(2):187–193. https://doi.org/10.1016/j.anai.2020.10.008.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Diver S, Khalfaoui L, Emson C, Wenzel SE, Menzies-Gow A et al. Effect of tezepelumab on airway inflammatory cells, remodelling, and hyperresponsiveness in patients with moderate-to-severe uncontrolled asthma (CASCADE): a double-blind, randomised, placebo-controlled, phase 2 trial. Lancet Respir Med. 2021;9(11):1299–1312. https://doi.org/10.1016/S2213-2600(21)00226-5.</mixed-citation><mixed-citation xml:lang="en">Diver S, Khalfaoui L, Emson C, Wenzel SE, Menzies-Gow A et al. Effect of tezepelumab on airway inflammatory cells, remodelling, and hyperresponsiveness in patients with moderate-to-severe uncontrolled asthma (CASCADE): a double-blind, randomised, placebo-controlled, phase 2 trial. Lancet Respir Med. 2021;9(11):1299–1312. https://doi.org/10.1016/S2213-2600(21)00226-5.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Menzies-Gow A, Corren J, Bourdin A, Chupp G, Israel E, Wechsler ME et al. Tezepelumab in Adults and Adolescents with Severe, Uncontrolled Asthma. N Engl J Med. 2021;384(19):1800–1809. https://doi.org/10.1056/NEJMoa2034975.</mixed-citation><mixed-citation xml:lang="en">Menzies-Gow A, Corren J, Bourdin A, Chupp G, Israel E, Wechsler ME et al. Tezepelumab in Adults and Adolescents with Severe, Uncontrolled Asthma. N Engl J Med. 2021;384(19):1800–1809. https://doi.org/10.1056/NEJMoa2034975.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Corren J, Parnes JR, Wang L, Mo M, Roseti SL, Griffiths JM, van der Merwe R. Tezepelumab in Adults with Uncontrolled Asthma. N Engl J Med. 2017;377(10):936–946. https://doi.org/10.1056/NEJMoa1704064.</mixed-citation><mixed-citation xml:lang="en">Corren J, Parnes JR, Wang L, Mo M, Roseti SL, Griffiths JM, van der Merwe R. Tezepelumab in Adults with Uncontrolled Asthma. N Engl J Med. 2017;377(10):936–946. https://doi.org/10.1056/NEJMoa1704064.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Castro M, Corren J, Pavord ID, Maspero J, Wenzel S, Rabe KF et al. Dupilumab Efficacy and Safety in Moderate-to-Severe Uncontrolled Asthma. N Engl J Med. 2018;378(26):2486–2496. https://doi.org/10.1056/NEJMoa1804092.</mixed-citation><mixed-citation xml:lang="en">Castro M, Corren J, Pavord ID, Maspero J, Wenzel S, Rabe KF et al. Dupilumab Efficacy and Safety in Moderate-to-Severe Uncontrolled Asthma. N Engl J Med. 2018;378(26):2486–2496. https://doi.org/10.1056/NEJMoa1804092.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Bleecker ER, FitzGerald JM, Chanez P, Papi A, Weinstein SF, Barker P et al. Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting β2 -agonists (SIROCCO): a randomised, multicentre, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2115–2127. https://doi.org/10.1016/S0140-6736(16)31324-1.</mixed-citation><mixed-citation xml:lang="en">Bleecker ER, FitzGerald JM, Chanez P, Papi A, Weinstein SF, Barker P et al. Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting β2 -agonists (SIROCCO): a randomised, multicentre, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2115–2127. https://doi.org/10.1016/S0140-6736(16)31324-1.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">FitzGerald JM, Bleecker ER, Nair P, Korn S, Ohta K, Lommatzsch MF et al. Benralizumab, an anti-interleukin-5 receptor α monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–2141. https://doi.org/10.1016/S0140-6736(16)31322-8.</mixed-citation><mixed-citation xml:lang="en">FitzGerald JM, Bleecker ER, Nair P, Korn S, Ohta K, Lommatzsch MF et al. Benralizumab, an anti-interleukin-5 receptor α monoclonal antibody, as add-on treatment for patients with severe, uncontrolled, eosinophilic asthma (CALIMA): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet. 2016;388(10056):2128–2141. https://doi.org/10.1016/S0140-6736(16)31322-8.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Ortega HG, Yancey SW, Mayer B, Gunsoy NB, Keene ON, Bleecker ER et al. Severe eosinophilic asthma treated with mepolizumab stratified by baseline eosinophil thresholds: a secondary analysis of the DREAM and MENSA studies. Lancet Respir Med. 2016;4(7):549–556. https://doi.org/10.1016/S2213-2600(16)30031-5.</mixed-citation><mixed-citation xml:lang="en">Ortega HG, Yancey SW, Mayer B, Gunsoy NB, Keene ON, Bleecker ER et al. Severe eosinophilic asthma treated with mepolizumab stratified by baseline eosinophil thresholds: a secondary analysis of the DREAM and MENSA studies. Lancet Respir Med. 2016;4(7):549–556. https://doi.org/10.1016/S2213-2600(16)30031-5.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Pham T-H, Ren P, Parnes JR, Griffiths JM. Tezepelumab reduces multiple key inflammatory biomarkers in patients with severe, uncontrolled asthma in the phase 2b PATHWAY study. Am J Respir Crit Care Med. 2019;199:A2677. https://doi.org/10.1164/ajrccm-conference.2019.199.1_MeetingAbstracts.A2677.</mixed-citation><mixed-citation xml:lang="en">Pham T-H, Ren P, Parnes JR, Griffiths JM. Tezepelumab reduces multiple key inflammatory biomarkers in patients with severe, uncontrolled asthma in the phase 2b PATHWAY study. Am J Respir Crit Care Med. 2019;199:A2677. https://doi.org/10.1164/ajrccm-conference.2019.199.1_MeetingAbstracts.A2677.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Janeway CA Jr, Travers P, Walport M, Shlomchik MJ. Immunobiology: the immune system in health and disease. 5th ed. New York: Garland Science; 2001. 910 p. Available at: https://www.ncbi.nlm.nih.gov/books/NBK27117/.</mixed-citation><mixed-citation xml:lang="en">Janeway CA Jr, Travers P, Walport M, Shlomchik MJ. Immunobiology: the immune system in health and disease. 5th ed. New York: Garland Science; 2001. 910 p. Available at: https://www.ncbi.nlm.nih.gov/books/NBK27117/.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Gauvreau GM, Sehmi R, Ambrose CS, Griffiths JM. Thymic stromal lymphopoietin: its role and potential as a therapeutic target in asthma. Expert Opin Ther Targets. 2020;24(8):777–792. https://doi.org/10.1080/14728222.2020.1783242.</mixed-citation><mixed-citation xml:lang="en">Gauvreau GM, Sehmi R, Ambrose CS, Griffiths JM. Thymic stromal lymphopoietin: its role and potential as a therapeutic target in asthma. Expert Opin Ther Targets. 2020;24(8):777–792. https://doi.org/10.1080/14728222.2020.1783242.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Gauvreau GM, Sehmi R, Ambrose CS, Griffiths JM. Thymic stromal lymphopoietin: its role and potential as a therapeutic target in asthma. Expert Opin Ther Targets. 2020;24(8):777–792. https://doi.org/10.1080/14728222.2020.1783242.</mixed-citation><mixed-citation xml:lang="en">Gauvreau GM, Sehmi R, Ambrose CS, Griffiths JM. Thymic stromal lymphopoietin: its role and potential as a therapeutic target in asthma. Expert Opin Ther Targets. 2020;24(8):777–792. https://doi.org/10.1080/14728222.2020.1783242.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Tanaka J, Watanabe N, Kido M, Saga K, Akamatsu T, Nishio A, Chiba T. Human TSLP and TLR3 ligands promote differentiation of Th17 cells with a central memory phenotype under Th2-polarizing conditions. Clin Exp Allergy. 2009;39(1):89–100. https://doi.org/10.1111/j.1365-2222.2008.03151.x.</mixed-citation><mixed-citation xml:lang="en">Tanaka J, Watanabe N, Kido M, Saga K, Akamatsu T, Nishio A, Chiba T. Human TSLP and TLR3 ligands promote differentiation of Th17 cells with a central memory phenotype under Th2-polarizing conditions. Clin Exp Allergy. 2009;39(1):89–100. https://doi.org/10.1111/j.1365-2222.2008.03151.x.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Allakhverdi Z, Comeau MR, Jessup HK, Delespesse G. Thymic stromal lymphopoietin as a mediator of crosstalk between bronchial smooth muscles and mast cells. J Allergy Clin Immunol. 2009;123(4):958.e2-960.e2. https://doi.org/10.1016/j.jaci.2009.01.059.</mixed-citation><mixed-citation xml:lang="en">Allakhverdi Z, Comeau MR, Jessup HK, Delespesse G. Thymic stromal lymphopoietin as a mediator of crosstalk between bronchial smooth muscles and mast cells. J Allergy Clin Immunol. 2009;123(4):958.e2-960.e2. https://doi.org/10.1016/j.jaci.2009.01.059.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
