<?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">nid</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология и диализ</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology and Dialysis</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1680-4422</issn><issn pub-type="epub">2618-9801</issn><publisher><publisher-name>Российское диализное общество</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.28996/2618-9801-2021-1-98-104</article-id><article-id custom-type="elpub" pub-id-type="custom">nid-12</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>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group></article-categories><title-group><article-title>Иммунологические факторы риска острого повреждения почек у больных пневмонией</article-title><trans-title-group xml:lang="en"><trans-title>Immunological risc factors for acute kidney damage in patients with pneumonia</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>Даминов</surname><given-names>Б. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Daminov</surname><given-names>B. T.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.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>Муминов</surname><given-names>Д. К.</given-names></name><name name-style="western" xml:lang="en"><surname>Muminov</surname><given-names>D. K.</given-names></name></name-alternatives><email xlink:type="simple">davron.muminov@yahoo.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>Даминова</surname><given-names>Л. Т.</given-names></name><name name-style="western" xml:lang="en"><surname>Daminova</surname><given-names>L. T.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Ташкентский Педиатрический медицинский институт</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tashkent Pediatric Medical Institute</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Ташкентский Государственный стоматологический институт</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Tashkent state dental Institute</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>21</day><month>06</month><year>2024</year></pub-date><volume>23</volume><issue>1</issue><fpage>98</fpage><lpage>104</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Даминов Б.Т., Муминов Д.К., Даминова Л.Т., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Даминов Б.Т., Муминов Д.К., Даминова Л.Т.</copyright-holder><copyright-holder xml:lang="en">Daminov B.T., Muminov D.K., Daminova L.T.</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://journal.nephro.ru/jour/article/view/12">https://journal.nephro.ru/jour/article/view/12</self-uri><abstract><p>Цель исследования: изучить иммунологические показатели у больных пневмонией на фоне ХБП и определить их значимость в развития острого повреждения почек. Материалы и методы: обследовано 120 больных внебольничной пневмонией: 40 больных пневмонией (группа Пн) и 80 больных пневмонией, которая развилась на фоне хронической болезни почек (группа Пн+ХБП). В качестве контрольной группы (КГ) было обследовано 20 здоровых лиц. В ходе исследования выявлено, что количество лейкоцитов в группе Пн+ХБП было выше на 162,24% чем в КГ (p&lt;0,001) и на 27,79% ниже чем в группе Пн (p&lt;0,001). У больных Пн отношение количества нейтрофилов к лимфоцитам достоверно увеличилось, а в группе Пн+ХБП осталось неизменным, несмотря на увеличение абсолютного числа лейкоцитов. У больных пневмонией с фоновой ХБП отмечалось наиболее выраженное увеличение доли Т-лимфоцитов за счет субпопуляции CD8 и CD95 клеток (p&lt;0,001 по сравнению с КГ и группой Пн) и преобладание увеличения IgG (p&lt;0,001). Из 120 больных пневмонией, включенных в исследование, у 97 больных (80,83%) было диагностировано острое повреждение почек (ОПП): у 75 больных - 1-й, у 15 больных - 2-й и у 7 больных - 3-й стадии. В группе больных пневмонией без фоновой патологии почек ОПП было диагностировано у 23 больных группы (57,5%), в группе Пн+ХБП - у 68 больных (85%) (хи-квадрат=10,80, p&lt;0,01). При проведении ретроспективного анализа исследуемых показателей в зависимости от развития ОПП и его степени тяжести были определены иммунологические предикторы развития ОПП. Выводы: внебольничная пневмония на фоне ХБП ассоциируется с истощением клеточного компонента неспецифического иммунитета, активацией приобретенного иммунитета вследствие хронического воспаления и хронической антигенной стимуляции. У больных пневмонией предикторами развития ОПП явились фоновая хроническая болезнь почек, высокие уровни реактивных и антителопродуцирующих лимфоцитов, моноцитов, незрелых гранулоцитов и ЦИК IgG, и уменьшенные уровни нейтрофилов и ЦИК IgМ.</p></abstract><trans-abstract xml:lang="en"><p>Purpose of the study was to assess the immunological parameters in patients with pneumonia and CKD in the background and to determine their significance in the development of acute kidney injury. Materials and methods: 120 patients with acute pneumonia were examined: 40 patients with pneumonia (group Pn) and 80 patients with pneumonia developed on the background of chronic kidney disease (group Pn+CKD); 20 healthy individuals were examined as a control group (CG). The number of leukocytes was increased in the group of Pn+CKD by 162.24% compared to the CG (p&lt;0.001) although was 27.79% lower than in the group of Pn (p&lt;0.001). In patients with Pn, the ratio of the number of neutrophils to lymphocytes increased significantly, and in the group of Pn+CKD, it remained unchanged, despite an increase in the absolute number of leukocytes. In patients with pneumonia with CKD in the background, the most pronounced increase in the proportion of T-lymphocytes was observed due to a subpopulation of CD8 and CD95 cells (p&lt;0.001 compared with CG and the Pn group) and the prevalence of an increase in IgG (p&lt;0.001). Among 120 patients with pneumonia included in the study, 97 patients (80.83%) were diagnosed with acute kidney injury (AKI): in 75 patients - the 1st stage, in 15 patients the 2nd stage and in 7 patients the 3rd one. In the group of patients with pneumonia without background renal pathology, AKI was diagnosed in 23 patients (57.5%), in the group of Pn+CKD - in 68 patients (85%, chi-square=10.80, p&lt;0.01). Immune predictors of AKI development depending on the development of AKI and its severity were determined by a retrospective analysis of the studied parameters. Conclusion: pneumonia associated with CKD is associated with the depletion of the cellular component of nonspecific immunity, activation of acquired immunity due to chronic inflammation and chronic antigenic stimulation. In patients with pneumonia, background chronic kidney disease, high levels of reactive and antibody-producing lymphocytes, monocytes, immature granulocytes and IgG CICs and decreased levels of neutrophils and IgM CICs were predictors of AKI.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>пневмония</kwd><kwd>функциональное состояние почек</kwd><kwd>острое повреждение почек</kwd><kwd>хронический болезнь почек</kwd><kwd>иммунограмма</kwd><kwd>pneumonia</kwd><kwd>functional state of the kidneys</kwd><kwd>acute kidney injury</kwd><kwd>chronic kidney disease</kwd><kwd>immunogram</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">World Health Organization. The top 10 causes of death. 2018 update. Available from: http://www.who.int Accessed 2018 Dec 12.</mixed-citation><mixed-citation xml:lang="en">World Health Organization. The top 10 causes of death. 2018 update. Available from: http://www.who.int Accessed 2018 Dec 12.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Murugan R. et al. Acute kidney injury in non-severe pneumonia is associated with an increased immune response and lower survival //Kidney international. - 2010. - Т. 77. - №. 6. - С. 527-535.</mixed-citation><mixed-citation xml:lang="en">Murugan R. et al. Acute kidney injury in non-severe pneumonia is associated with an increased immune response and lower survival //Kidney international. - 2010. - Т. 77. - №. 6. - С. 527-535.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Bernard G. R. et al. Efficacy and safety of recombinant human activated protein C for severe sepsis //New England journal of medicine. - 2001. - Т. 344. - №. 10. - С. 699-709.</mixed-citation><mixed-citation xml:lang="en">Bernard G. R. et al. Efficacy and safety of recombinant human activated protein C for severe sepsis //New England journal of medicine. - 2001. - Т. 344. - №. 10. - С. 699-709.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Bagshaw S. M. et al. Early acute kidney injury and sepsis: a multicentre evaluation //Critical care. - 2008. - Т. 12. - №. 2. - С. R47.</mixed-citation><mixed-citation xml:lang="en">Bagshaw S. M. et al. Early acute kidney injury and sepsis: a multicentre evaluation //Critical care. - 2008. - Т. 12. - №. 2. - С. R47.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Bihorac A. et al. Long-term risk of mortality and acute kidney injury during hospitalization after major surgery //Annals of surgery. - 2009. - Т. 249. - №. 5. - С. 851-858.</mixed-citation><mixed-citation xml:lang="en">Bihorac A. et al. Long-term risk of mortality and acute kidney injury during hospitalization after major surgery //Annals of surgery. - 2009. - Т. 249. - №. 5. - С. 851-858.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Coca S. G. et al. Long-term risk of mortality and other adverse outcomes after acute kidney injury: a systematic review and meta-analysis //American journal of kidney diseases. - 2009. - Т. 53. - №. 6. - С. 961-973.</mixed-citation><mixed-citation xml:lang="en">Coca S. G. et al. Long-term risk of mortality and other adverse outcomes after acute kidney injury: a systematic review and meta-analysis //American journal of kidney diseases. - 2009. - Т. 53. - №. 6. - С. 961-973.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Alobaidi R. et al. Sepsis-associated acute kidney injury //Seminars in nephrology. - WB Saunders, 2015. - Т. 35. - №. 1. - С. 2-11.</mixed-citation><mixed-citation xml:lang="en">Alobaidi R. et al. Sepsis-associated acute kidney injury //Seminars in nephrology. - WB Saunders, 2015. - Т. 35. - №. 1. - С. 2-11.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Серов В. А. и др. Прогностическое значение острого повреждения почек у больных внебольничной пневмонией //Терапевтический архив (архив до 2018 г.). - 2016. - Т. 88. - №. 6. - С. 9-13.</mixed-citation><mixed-citation xml:lang="en">Серов В. А. и др. Прогностическое значение острого повреждения почек у больных внебольничной пневмонией //Терапевтический архив (архив до 2018 г.). - 2016. - Т. 88. - №. 6. - С. 9-13.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Kato S. et al. Aspects of immune dysfunction in end-stage renal disease //Clinical Journal of the American Society of Nephrology. - 2008. - Т. 3. - №. 5. - С. 1526-1533.</mixed-citation><mixed-citation xml:lang="en">Kato S. et al. Aspects of immune dysfunction in end-stage renal disease //Clinical Journal of the American Society of Nephrology. - 2008. - Т. 3. - №. 5. - С. 1526-1533.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Janeway Jr C. A., Medzhitov R. Innate immune recognition //Annual review of immunology. - 2002. - Т. 20. - №. 1. - С. 197-216.</mixed-citation><mixed-citation xml:lang="en">Janeway Jr C. A., Medzhitov R. Innate immune recognition //Annual review of immunology. - 2002. - Т. 20. - №. 1. - С. 197-216.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Kamata H. et al. Epithelial cell-derived secreted and transmembrane 1a signals to activated neutrophils during pneumococcal pneumonia //American journal of respiratory cell and molecular biology. - 2016. - Т. 55. - №. 3. - С. 407-418.</mixed-citation><mixed-citation xml:lang="en">Kamata H. et al. Epithelial cell-derived secreted and transmembrane 1a signals to activated neutrophils during pneumococcal pneumonia //American journal of respiratory cell and molecular biology. - 2016. - Т. 55. - №. 3. - С. 407-418.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Quinton L. J., Mizgerd J. P. Dynamics of lung defense in pneumonia: resistance, resilience, and remodeling //Annual review of physiology. - 2015. - Т. 77. - С. 407-430.</mixed-citation><mixed-citation xml:lang="en">Quinton L. J., Mizgerd J. P. Dynamics of lung defense in pneumonia: resistance, resilience, and remodeling //Annual review of physiology. - 2015. - Т. 77. - С. 407-430.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Viasus D. et al. Epidemiology, clinical features and outcomes of pneumonia in patients with chronic kidney disease //Nephrology Dialysis Transplantation. - 2011. - Т. 26. - №. 9. - С. 2899-2906.</mixed-citation><mixed-citation xml:lang="en">Viasus D. et al. Epidemiology, clinical features and outcomes of pneumonia in patients with chronic kidney disease //Nephrology Dialysis Transplantation. - 2011. - Т. 26. - №. 9. - С. 2899-2906.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Kotton D. N., Morrisey E. E. Lung regeneration: mechanisms, applications and emerging stem cell populations //Nature medicine. - 2014. - Т. 20. - №. 8. - С. 822-832.</mixed-citation><mixed-citation xml:lang="en">Kotton D. N., Morrisey E. E. Lung regeneration: mechanisms, applications and emerging stem cell populations //Nature medicine. - 2014. - Т. 20. - №. 8. - С. 822-832.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Linkermann A. et al. Regulated cell death and inflammation: an auto-amplification loop causes organ failure //Nature Reviews Immunology. - 2014. - Т. 14. - №. 11. - С. 759-767.</mixed-citation><mixed-citation xml:lang="en">Linkermann A. et al. Regulated cell death and inflammation: an auto-amplification loop causes organ failure //Nature Reviews Immunology. - 2014. - Т. 14. - №. 11. - С. 759-767.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Mitra A., Raychaudhuri S. K., Raychaudhuri S. P. IL-22 induced cell proliferation is regulated by PI3K/Akt/mTOR signaling cascade //Cytokine. - 2012. - Т. 60. - №. 1. - С. 38-42.</mixed-citation><mixed-citation xml:lang="en">Mitra A., Raychaudhuri S. K., Raychaudhuri S. P. IL-22 induced cell proliferation is regulated by PI3K/Akt/mTOR signaling cascade //Cytokine. - 2012. - Т. 60. - №. 1. - С. 38-42.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Su L., Xie L., Liu D. Urine sTREM-1 may be a valuable biomarker in diagnosis and prognosis of sepsis-associated acute kidney injury //Critical care. - 2015. - Т. 19. - №. 1. - С. 281.</mixed-citation><mixed-citation xml:lang="en">Su L., Xie L., Liu D. Urine sTREM-1 may be a valuable biomarker in diagnosis and prognosis of sepsis-associated acute kidney injury //Critical care. - 2015. - Т. 19. - №. 1. - С. 281.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kim J. U. et al. Dendritic cell dysfunction in patients with end-stage renal disease //Immune network. - 2017. - Т. 17. - №. 3. - С. 152-162.</mixed-citation><mixed-citation xml:lang="en">Kim J. U. et al. Dendritic cell dysfunction in patients with end-stage renal disease //Immune network. - 2017. - Т. 17. - №. 3. - С. 152-162.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Rossaint J. et al. FGF23 signaling impairs neutrophil recruitment and host defense during CKD //The Journal of clinical investigation. - 2016. - Т. 126. - №. 3. - С. 962-974.</mixed-citation><mixed-citation xml:lang="en">Rossaint J. et al. FGF23 signaling impairs neutrophil recruitment and host defense during CKD //The Journal of clinical investigation. - 2016. - Т. 126. - №. 3. - С. 962-974.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Lech M., Rommele C., Anders H. J. Pentraxins in nephrology: C-reactive protein, serum amyloid P and pentraxin-3 //Nephrology dialysis transplantation. - 2013. - Т. 28. - №. 4. - С. 803-811.</mixed-citation><mixed-citation xml:lang="en">Lech M., Rommele C., Anders H. J. Pentraxins in nephrology: C-reactive protein, serum amyloid P and pentraxin-3 //Nephrology dialysis transplantation. - 2013. - Т. 28. - №. 4. - С. 803-811.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Huen S. C., Cantley L. G. Macrophages in renal injury and repair //Annual review of physiology. - 2017. - Т. 79. - С. 449-469.</mixed-citation><mixed-citation xml:lang="en">Huen S. C., Cantley L. G. Macrophages in renal injury and repair //Annual review of physiology. - 2017. - Т. 79. - С. 449-469.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Weller S., Varrier M., Ostermann M. Lymphocyte function in human acute kidney injury //Nephron. - 2017. - Т. 137. - №. 4. - С. 287-293.</mixed-citation><mixed-citation xml:lang="en">Weller S., Varrier M., Ostermann M. Lymphocyte function in human acute kidney injury //Nephron. - 2017. - Т. 137. - №. 4. - С. 287-293.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Nakazawa D. et al. Histones and neutrophil extracellular traps enhance tubular necrosis and remote organ injury in ischemic AKI //Journal of the American society of nephrology. - 2017. - Т. 28. - №. 6. - С. 1753-1768.</mixed-citation><mixed-citation xml:lang="en">Nakazawa D. et al. Histones and neutrophil extracellular traps enhance tubular necrosis and remote organ injury in ischemic AKI //Journal of the American society of nephrology. - 2017. - Т. 28. - №. 6. - С. 1753-1768.</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>
