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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">mimmun</journal-id><journal-title-group><journal-title xml:lang="ru">Медицинская иммунология</journal-title><trans-title-group xml:lang="en"><trans-title>Medical Immunology (Russia)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1563-0625</issn><issn pub-type="epub">2313-741X</issn><publisher><publisher-name>SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.15789/1563-0625-2019-4-595-602</article-id><article-id custom-type="elpub" pub-id-type="custom">mimmun-1620</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>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>ЗАВИСИМОЕ ОТ ЛЕКТИНОВ РАЗНООБРАЗИЕ ПОПУЛЯЦИЙ ПРИРОДНЫХ КИЛЛЕРНЫХ КЛЕТОК В КОММУНИКАЦИЯХ ПРОТИВ ОПУХОЛЕЙ И ВИРУСОВ</article-title><trans-title-group xml:lang="en"><trans-title>LECTIN-DEPENDENT DIVERSITY OF NATURAL KILLER POPULATIONS AND COMMUNICATIONS AGAINST TUMORS AND VIRUSES</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Лахтин</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Lakhtin</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>к.б.н., старший научный сотрудник</p><p>125212, Россия, Москва, ул. Адмирала Макарова, 10</p><p>+7 (495) 452-18-16</p></bio><bio xml:lang="en"><p>PhD (Medicine), Senior Research Associate</p><p>125212, Russian Federation, Moscow, Adm. Makarov str., 10</p><p>+7 (495) 452-18-16</p></bio><email xlink:type="simple">info@gabrich.com</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>Лахтин</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Lakhtin</surname><given-names>V. M.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.б.н., главный научный сотрудник</p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Chief Research Associate, G.N. Gabrichevsky Research Institute for Epidemiology and Microbiology,</p><p>Moscow</p></bio><email xlink:type="simple">Lakhtinv@yandex.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>Алешкин</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Aleshkin</surname><given-names>V. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.б.н., профессор, научный руководитель</p></bio><bio xml:lang="en"><p>PhD, MD Professor (Medicine), Research Director</p><p>Moscow</p></bio><email xlink:type="simple">info@gabrich.com</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>Афанасьев</surname><given-names>С. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Afanasiev</surname><given-names>S. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>д.м.н., профессор, главный научный сотрудник </p></bio><bio xml:lang="en"><p>PhD, MD (Medicine), Chief Research Associate – Doctor of Medical Sciences, Professor, Chief Research Officer</p><p>Moscow</p></bio><email xlink:type="simple">afanasievss409.4@bk.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФБУН «Московский научно-исследовательский институт эпидемиологии и микробиологии имени Г.Н. Габричевского» Роспотребнадзора</institution><country>Россия</country></aff><aff xml:lang="en"><institution>G.N. Gabrichevsky Research Institute for Epidemiology and Microbiology</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>11</day><month>03</month><year>2019</year></pub-date><volume>21</volume><issue>4</issue><issue-title>препринт</issue-title><fpage>595</fpage><lpage>602</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Лахтин М.В., Лахтин В.М., Алешкин В.А., Афанасьев С.С., 2019</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="ru">Лахтин М.В., Лахтин В.М., Алешкин В.А., Афанасьев С.С.</copyright-holder><copyright-holder xml:lang="en">Lakhtin M.V., Lakhtin V.M., Aleshkin V.A., Afanasiev S.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.mimmun.ru/mimmun/article/view/1620">https://www.mimmun.ru/mimmun/article/view/1620</self-uri><abstract><p>Популяции природных киллерных клеток человека (ППККЧ) против опухолей в присутствии вирусов оценены как сильно варьирующие и рано адаптированные к патологическим сигналам в организме мобильные и избирательно действующие способные к комбинированию агенты. ППККЧ осуществляют различные действия в результате кофункционирования рецепторных лектинов (РЛ), распознающих гликопаттерны (РЛ как триггеры, инициаторы и базисные агенты для надстроечных реакций), и Ig-подобных, цитотоксических и прочих вспомогательных коммуникативных и эффекторных рецепторов (роль РЛ как инструментов тонкой настройки мозаики поверхностноклеточных рецепторов в направлении необходимой функциональной ориентации ППККЧ), а также их лигандов (модуляторов созданных конечных рецепторных мозаик). Такие наученные и переобученные ППККЧ играют важную роль в перераспределении ППККЧ-индуцированных паротиворопухолевых и антивирусных цитокиновых наборов в организме. Межклеточный коммуникативный потенциал ППККЧ также учитывает другие клетки врожденного иммунитета и адаптированные для врожденного иммунитета клетки, что может служить перспективным и универсальным ресурсом защиты человека. ППККЧ должны учитываться при разработке товых маневренных и надежных сбалансированных профилактических и иммунотерапевтических противоопухолевых/ антивирусных систем и вакцинных стратегий. Открыты пути к алгоритмам тонкой настройки (РЛ—KIR/ NCR/ CD/ их комбинации)  РЛ-базисного конструирования веера противоопухолевых/ антивирусных ППККЧ с дальнейшим потенциалом инициирования. Ключевую важность приобретает скрининг спектра ППККЧ у индивидуума и потенциального пациента для дополнительной оценки защитного статуса и выработки персонизированных коммуникативных противоопухолевых/ антивирусных стратегий. Установленный статус NK(natural killers)-компартмента будет характеризовать резистентность индивидуума/ контингента индивидуумов против вирусных инфекаций эпидемиологической значимости, играть важную роль при оценке противоэпидемической защиты региона.</p><p> </p></abstract><trans-abstract xml:lang="en"><p>Response of human natural killer (NK) cell populations (NKP) against tumors in the presence of viruses was evaluated as a quite variable, early adapting for the pathological signals in organism, mobile and selective combination agents. NKP act as a result of co-functioning between the receptor lectins (RL) recognizing glycopatterns (RL as triggers, initiators and basic agents for coupled activities), and Ig-like, cytotoxic and other additional  communicative and effector receptors (superstructural, tuning for achievement of final effector-type NKP constructions required), and their ligands (modulators of final cell surface receptor mosaics). Such NKP created play important role in redistribution of NKP-induced antitumor/ antiviral cytokines in organism. Intercellular communicative potential of NKP also involves other innate and innate-like cells. Such extended communications of NKP provide a prospective and universal resource of human protection. NKP must be under consideration upon development of new maneuvre and relilable prophylactic and immunotherapeutic antitumor/ antiviral systems and vaccine strategies. The ways for the fine tuning (RL—KIR/ NCR/ CD/ their combinations) algorithms of RL-based creation of antitumor/ antiviral NKP are revealed. Key role is given to screening spectrum of patient NKP for development of communicative anticancer/ antiviral strategies. The status of NK compartment will characterize resistance of individuum/ contingent of individuums to viral infections of epidemiological significance, will play important role in anti-epidemic protection of regional population.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>популяции киллерных клеток</kwd><kwd>рецепторные лектины</kwd><kwd>гликоконъюгаты</kwd><kwd>цитокины</kwd><kwd>врожденный иммунитет</kwd><kwd>мукозальный иммунитет</kwd><kwd>дисбиозы</kwd><kwd>пробиотические лектины</kwd><kwd>противоопухолевые стратегии</kwd><kwd>антивирусные стратегии</kwd></kwd-group><kwd-group xml:lang="en"><kwd>cells</kwd><kwd>NK cell populations</kwd><kwd>receptor lectins</kwd><kwd>glycoconjugates</kwd><kwd>cytokines</kwd><kwd>innate immunity</kwd><kwd>mucosal immunity</kwd><kwd>dysbioses</kwd><kwd>probiotic lectins</kwd><kwd>antitumor strategies</kwd><kwd>antiviral strategies</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">Лахтин М.В., Лахтин В.М., Алёшкин В.А., Афанасьев М.С., Афанасьев С.С. 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