<?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="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</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">749</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2008-0-4-26-30</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>HEMATOPOIETIC STEM CELL TRANSPLANTATION</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ТРАНСПЛАНТАЦИЯ ГЕМОПОЭТИЧЕСКИХ СТВОЛОВЫХ КЛЕТОК</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Determination of eosinophilic cationic protein and tryptase in graft versus host disease and hematological malignancies with eosinophilia</article-title><trans-title-group xml:lang="ru"><trans-title>Определение эозинофильного катионного белка и триптазы при хронической реакции «трансплантат против хозяина» и гемобластозах с эозинофилией</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Komarova</surname><given-names>L. S.</given-names></name><name xml:lang="ru"><surname>Комарова</surname><given-names>Л. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Saint-Petersburg</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mikhailova</surname><given-names>N. B.</given-names></name><name xml:lang="ru"><surname>Михайлова</surname><given-names>Н. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Saint-Petersburg</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Totolyan</surname><given-names>A. A.</given-names></name><name xml:lang="ru"><surname>Тотолян</surname><given-names>А. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Saint-Petersburg</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Afanasyev</surname><given-names>B. V.</given-names></name><name xml:lang="ru"><surname>Афанасьев</surname><given-names>Б. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Saint-Petersburg</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Saint-Petersburg Pavlov State Medical University</institution></aff><aff><institution xml:lang="ru">Санкт-Петербургский государственный медицинский университет им. акад. И.П. Павлова</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2008-11-25" publication-format="electronic"><day>25</day><month>11</month><year>2008</year></pub-date><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>26</fpage><lpage>30</lpage><history><date date-type="received" iso-8601-date="2022-11-25"><day>25</day><month>11</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-11-25"><day>25</day><month>11</month><year>2022</year></date></history><permissions><copyright-year>2008</copyright-year><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/749">https://oncohematology.abvpress.ru/ongm/article/view/749</self-uri><abstract xml:lang="en"><p>Diseases with eosinophilia the pathogenesis of which is unclear are of particular clinical significance among hematological malignancies. These include acute and chronic graft versus host disease (GVHD) associated with eosinophilia, hypereosinophilic syndrome and chronic myeloid leukemias, Hodgkin's and non-Hodgkin's lymphomas. The role of eosinophils and mast cells intracellular proteins in proliferative diseases is unknown. The objective of the investigation was to study the significance of tryptase and eosinophilic cationic protein (ECP) measurements in patients with chronic GVHD and hematological malignancies. Thirty two patients with verified oncohematological diseases (a study group) — 6 patients with chronic GVHD after allogeneic hemopoietic stem cells transplantation, 18 with asthma and 8 with solid tumors - were included in the study. The serum concentrations of tryptase and ECP were measured by immunofluorescence assay. Elevated ECP levels were found in patients with GVHD (p &lt; 0.03) and in those with lymphoproliferative diseases (p = 0.007) as compared to the nonhematological group (p &lt; 0.03). Increased tryptase level was recorded in patients with GVHD and lymphoproliferative diseases as compared to those with solid tumors and nonhematological disorders (p = 0.03), as well as in the GVHD versus lymphoproliferation groups (p &lt; 0.05). A direct correlation between ECP concentration and the eosinophils count in patients with lymphoproliferative diseases (r = 0.9; p = 0.000001) was found. The authors have concluded that measurement of soluble eosinophilic proteins levels and mast cell enzymes is reasonable to diagnostics and monitoring of various hypereosinophilic states in patients with chronic GVHD and hematological malignancies.</p></abstract><trans-abstract xml:lang="ru"><p>Особую клиническую значимость среди гемобластозов представляют заболевания с высокой степенью эозинофилии, патогенез которой неясен. К ним относятся острая и хроническая реакции «трансплантат против хозяина» (РТПХ), ассоциированные с эозинофилией, гиперэозинофильный синдром и хронические миелоидные лейкозы, ходжкинские и неходжкинские лимфомы. Роль внутриклеточных белков эозинофилов и тучных клеток при заболеваниях пролиферативного происхождения не совсем ясна. Цель работы состояла в изучении значимости количественного определения триптазы и эозинофильного катионного белка (ЕСР) у пациентов с хронической РТПХ и гемобластозами. В исследование были включены 32 пациента с верифицированными онкогематологическими заболеваниями (основная группа): 6 — с хронической РТПХ после аллогенной трансплантации гемопоэтических стволовых клеток, 18 — с бронхиальной астмой и 8 — с солидными опухолями. Определение концентрации триптазы и ЕСР в сыворотке крови осуществлено методом иммунофлюоресцентного анализа. Повышенный уровень ЕСР выявлен у больных с РТПХ (р&lt;0,03) и в группе лимфопролиферации (р=0,007) по сравнению с негематологической группой (р&lt;0,03). Повышенный уровень триптазы зафиксирован в группах РТПХ и лимфопролиферации по сравнению с группой солидных опухолей и негематологической (р=0,03), а также при РТПХ по сравнению с группой лимфопролиферации (р&lt;0,05). Обнаружена прямая зависимость между концентрацией ЕСР и абсолютным содержанием эозинофилов в крови пациентов с лимфопролиферативными заболеваниями (r=0,9; р=0,000001). Определение уровня растворимых белков эозинофилов и ферментов тучных клеток целесообразно использовать для диагностики и мониторинга различных гиперэозинофильных состояний при ведении пациентов с хронической РТПХ и гемобластозами.</p></trans-abstract><kwd-group xml:lang="en"><kwd>eosinophilic cationic protein</kwd><kwd>tryptase</kwd><kwd>eosinophilia</kwd><kwd>graft versus host disease</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>эозинофильный катионный белок</kwd><kwd>триптаза</kwd><kwd>эозинофилия</kwd><kwd>РТПХ</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Ellyard J.I., Simson L., Parish C.R. Th2-mediated anti-tumor immunity: friend or foe? J compilat 2007;70:1—11.</mixed-citation><mixed-citation xml:lang="ru">Ellyard J.I., Simson L., Parish C.R. Th2-mediated anti-tumor immunity: friend or foe? J compilat 2007;70:1—11.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Фрейдлин И.С., Тотолян А.А. Клетки иммунной системы. СПб.: Наука, 2000. Т. 3—5.</mixed-citation><mixed-citation xml:lang="ru">Фрейдлин И.С., Тотолян А.А. Клетки иммунной системы. СПб.: Наука, 2000. Т. 3—5.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. McNeel D., Rubio M.T., Damaj G. Hypereosinophilia as a presenting sign of acute graft-versus-host disease after allogenic bone marrow transplantation. Transplantation 2002;74:1797.</mixed-citation><mixed-citation xml:lang="ru">McNeel D., Rubio M.T., Damaj G. Hypereosinophilia as a presenting sign of acute graft-versus-host disease after allogenic bone marrow transplantation. Transplantation 2002;74:1797.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Комарова Л.С., Зуева Е.Е., Нестерович И.И. и др. Роль внутриклеточных белков эозинофилов и тучных клеток в развитии эозинофилии при различных заболеваниях. Рос иммунол журн 2007;1(10):27—33.</mixed-citation><mixed-citation xml:lang="ru">Комарова Л.С., Зуева Е.Е., Нестерович И.И. и др. Роль внутриклеточных белков эозинофилов и тучных клеток в развитии эозинофилии при различных заболеваниях. Рос иммунол журн 2007;1(10):27—33.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Shakoory B., Fitzgerald S.M., Lee S.A. et al. The role of human mast cell derived cytokines in eosinophil biology. J Interferon and Cytokine Res 2004;24:271—81.</mixed-citation><mixed-citation xml:lang="ru">Shakoory B., Fitzgerald S.M., Lee S.A. et al. The role of human mast cell derived cytokines in eosinophil biology. J Interferon and Cytokine Res 2004;24:271—81.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Hallgren J., Pejler G. Biology of mast cell tryptase: an inflammatory mediator. FEBS J 2006; 25:234—41.</mixed-citation><mixed-citation xml:lang="ru">Hallgren J., Pejler G. Biology of mast cell tryptase: an inflammatory mediator. FEBS J 2006; 25:234—41.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Fletchera S., Bain B. Diagnosis and treatment of hypereosinophilic syndromes. Current Opinion in Hematology 2007;14(1):37—42.</mixed-citation><mixed-citation xml:lang="ru">Fletchera S., Bain B. Diagnosis and treatment of hypereosinophilic syndromes. Current Opinion in Hematology 2007;14(1):37—42.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Реброва О.Ю. Статистический анализ медицинских данных. Применение пакета прикладных программ STATISTICA. М.: МедиаСфера, 2003.</mixed-citation><mixed-citation xml:lang="ru">Реброва О.Ю. Статистический анализ медицинских данных. Применение пакета прикладных программ STATISTICA. М.: МедиаСфера, 2003.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Ayalew T.A., Patnaik M.M., Pardanani A. Eosinophilia: secondary, clonal and idiopathic. Br J Haematol 2006;133:468—92.</mixed-citation><mixed-citation xml:lang="ru">Ayalew T.A., Patnaik M.M., Pardanani A. Eosinophilia: secondary, clonal and idiopathic. Br J Haematol 2006;133:468—92.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Gotlib J., Cross N.C.P., Gilliland D.G. Eosinophilic disorders: molecular pathogenesis, new classification, and modern therapy. Best Pract Res Clin Haematol 2006;19(3):535—69.</mixed-citation><mixed-citation xml:lang="ru">Gotlib J., Cross N.C.P., Gilliland D.G. Eosinophilic disorders: molecular pathogenesis, new classification, and modern therapy. Best Pract Res Clin Haematol 2006;19(3):535—69.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Sade K., Mysels A., Levo Y. et al. Eosinophilia: A study of 100 hospitalized patients. Eur J Intern Med 2007;18:196—201.</mixed-citation><mixed-citation xml:lang="ru">Sade K., Mysels A., Levo Y. et al. Eosinophilia: A study of 100 hospitalized patients. Eur J Intern Med 2007;18:196—201.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Ringden O. Immunotherapy by allogeneic stem cell transplantation. Adv Cancer Res 2007;97:25—60.</mixed-citation><mixed-citation xml:lang="ru">Ringden O. Immunotherapy by allogeneic stem cell transplantation. Adv Cancer Res 2007;97:25—60.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Jacobsohn D.A., Schechter T., Seshadri R. et al. Eosinophillia correlates with the presence or development of chronic graft-versus-host disease in children. Transplantation 2004;77(7):1096—100.</mixed-citation><mixed-citation xml:lang="ru">Jacobsohn D.A., Schechter T., Seshadri R. et al. Eosinophillia correlates with the presence or development of chronic graft-versus-host disease in children. Transplantation 2004;77(7):1096—100.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Aisa Y., Mori T., Nakazato T. et al. Blood eosinophilia as a marker of favorable outcome after allogeneic stem cell transplantation. J compilat Eur Soc for Org Transpl 2007;20:761—70.</mixed-citation><mixed-citation xml:lang="ru">Aisa Y., Mori T., Nakazato T. et al. Blood eosinophilia as a marker of favorable outcome after allogeneic stem cell transplantation. J compilat Eur Soc for Org Transpl 2007;20:761—70.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Lotfi R., Lee J.J., Lotze M.T. Eosinophilic granulocytes and damageassociated molecular pattern molecules (DAMPs). Role in the inflammatory response within tumors. J Immunother 2007;30:116—28.</mixed-citation><mixed-citation xml:lang="ru">Lotfi R., Lee J.J., Lotze M.T. Eosinophilic granulocytes and damageassociated molecular pattern molecules (DAMPs). Role in the inflammatory response within tumors. J Immunother 2007;30:116—28.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Mingomataj E.C. Eosinophil-induced prognosis improvement of solid tumors could be enabled by their vesicle-mediated barrier permeability induction. Med Hypoth 2008;70(3):582—4.</mixed-citation><mixed-citation xml:lang="ru">Mingomataj E.C. Eosinophil-induced prognosis improvement of solid tumors could be enabled by their vesicle-mediated barrier permeability induction. Med Hypoth 2008;70(3):582—4.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Puxeddu I., Alian A., Piliponsky A.M. et al. Human peripheral blood eosinophils induce angiogenesis. Int J Biochem Cell Biol 2005;37:628—36.</mixed-citation><mixed-citation xml:lang="ru">Puxeddu I., Alian A., Piliponsky A.M. et al. Human peripheral blood eosinophils induce angiogenesis. Int J Biochem Cell Biol 2005;37:628—36.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Sperr W.R., Hauswirth A.W., Valent P. Tryptase a novel biochemical marker of acute myeloid leukemia. Leuk Lymph 2002;43(12):2257—61.</mixed-citation><mixed-citation xml:lang="ru">Sperr W.R., Hauswirth A.W., Valent P. Tryptase a novel biochemical marker of acute myeloid leukemia. Leuk Lymph 2002;43(12):2257—61.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Carvalho R.F.S., Mahshid Y., Claesson H.-E. et al. Expression of mast cell tryptases in Hodgkin and reed-sternberg (HRS) cells. J compilat Scand J Immunol 2007;67:53—6.</mixed-citation><mixed-citation xml:lang="ru">Carvalho R.F.S., Mahshid Y., Claesson H.-E. et al. Expression of mast cell tryptases in Hodgkin and reed-sternberg (HRS) cells. J compilat Scand J Immunol 2007;67:53—6.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Molin D., Edstrom A., Glimelius I. et al. Mast cell infiltration correlates with poor prognosis in Hodgkin's lymphoma. Br J Haematol 2002;119(1):122—4.</mixed-citation><mixed-citation xml:lang="ru">Molin D., Edstrom A., Glimelius I. et al. Mast cell infiltration correlates with poor prognosis in Hodgkin's lymphoma. Br J Haematol 2002;119(1):122—4.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Molin D., Fischer M., Xiang Z. et al. Mast cells express functional CD30 ligand and are the predominant CD30 L-positive cells in Hodgkin's disease. Br J Haematol 2001;114:616—23.</mixed-citation><mixed-citation xml:lang="ru">Molin D., Fischer M., Xiang Z. et al. Mast cells express functional CD30 ligand and are the predominant CD30 L-positive cells in Hodgkin's disease. Br J Haematol 2001;114:616—23.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Sperr W.R., Stehberger B., Wimazal F. Serum tryptase measurements in patients with myelodysplastic syndromes. Leuk Lymphoma 2002;43:1097—105.</mixed-citation><mixed-citation xml:lang="ru">Sperr W.R., Stehberger B., Wimazal F. Serum tryptase measurements in patients with myelodysplastic syndromes. Leuk Lymphoma 2002;43:1097—105.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
