<?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">Pediatric Hematology/Oncology and Immunopathology</journal-id><journal-title-group><journal-title xml:lang="en">Pediatric Hematology/Oncology and Immunopathology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы гематологии/онкологии и иммунопатологии в педиатрии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-1708</issn><issn publication-format="electronic">2414-9314</issn><publisher><publisher-name xml:lang="en">Fund Doctors, Innovations, Science for Children</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">439</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2020-19-4-234-242</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Erythrocyte as an ideal carrier for intavascular drug delivery</article-title><trans-title-group xml:lang="ru"><trans-title>Эритроцит как идеальный носитель для внутрисосудистой доставки лекарств</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8803-5694</contrib-id><name-alternatives><name xml:lang="en"><surname>Koleva</surname><given-names>L. D.</given-names></name><name xml:lang="ru"><surname>Колева</surname><given-names>Л. Д.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p><bold>Larisa D. Koleva</bold>, junior researcher of the Laboratory of Biophysics</p><p>1 Samory Mashela St., Moscow 117997 </p></bio><bio xml:lang="ru"><p><bold>Колева Лариса Дмитриевна</bold>, младший научный сотрудник лаборатории биофизики </p><p>117997, Москва, ул. Саморы Машела, 1</p></bio><email>larulea@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3403-181X</contrib-id><name-alternatives><name xml:lang="en"><surname>Ataullakhanov</surname><given-names>F. I.</given-names></name><name xml:lang="ru"><surname>Атауллаханов</surname><given-names>Ф. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5948-3444</contrib-id><name-alternatives><name xml:lang="en"><surname>Sinauridze</surname><given-names>E. I.</given-names></name><name xml:lang="ru"><surname>Синауридзе</surname><given-names>Е. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Moscow</p></bio><bio xml:lang="ru"><p>Москва</p></bio><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Healthcare of the Russian Federation</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Center for Theoretical Problems of Physical and Chemical Pharmacology, Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">ФГБУН «Центр теоретических проблем физико-химической фармакологии» РАН</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Lomonosov Moscow State University</institution></aff><aff><institution xml:lang="ru">ФГБОУ ВО «Московский государственный университет им. М.В. Ломоносова»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2020-12-08" publication-format="electronic"><day>08</day><month>12</month><year>2020</year></pub-date><volume>19</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>234</fpage><lpage>242</lpage><history><date date-type="received" iso-8601-date="2020-12-22"><day>22</day><month>12</month><year>2020</year></date><date date-type="accepted" iso-8601-date="2020-12-22"><day>22</day><month>12</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">«D. Rogachev NMRCPHOI»</copyright-holder><copyright-holder xml:lang="ru">ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://hemoncim.com/jour/article/view/439">https://hemoncim.com/jour/article/view/439</self-uri><abstract xml:lang="en"><p>Drug delivery using natural biological carriers, especially erythrocytes, is a rapidly developing field. Erythrocytes can act as carriers with the gradual release of a pharmacological agent, as bioreactors with encapsulated enzymes, or as a tool for targeted delivery of drugs to target organs especially tissue macrophages, liver and spleen. To date, red blood cells have been studied as carriers for a wide range of drug compounds, such as enzymes, antibiotics, anti-inflammatory, antiviral drugs, etc. The review is devoted to the advantages of erythrocytes as carriers for the delivery of drugs loaded into the erythrocyte, or related to its surface, and defines the main directions of research on erythrocytes carriers of biologically active substances. Particular attention is paid to in vivo studies that reveal the potential of carrier erythrocytes for clinical use.</p></abstract><trans-abstract xml:lang="ru"><p>Доставка лекарств с использованием природных биологических носителей, в частности эритроцитов, является быстро развивающейся областью изучения. Эритроциты могут действовать как носители с постепенным высвобождением фармакологического агента, в качестве биореакторов с инкапсулированными ферментами или в качестве инструмента для направленной доставки лекарств в органы-мишени, прежде всего в тканевые макрофаги, печень и селезенку. На сегодняшний день эритроциты изучены в качестве носителей для широкого спектра лекарственных соединений, таких как ферменты, антибиотики, противовоспалительные, противовирусные препараты и т. д. Обзор посвящен преимуществам эритроцитов как носителей для доставки лекарств, загруженных в них, или связанных с их поверхностью, и определяет основные направления исследований эритроцитов-носителей биологически активных веществ. Особое внимание уделяется исследованиям in vivo, раскрывающим потенциал эритроцитов-носителей для клинического применения.</p></trans-abstract><kwd-group xml:lang="en"><kwd>antitumor therapy</kwd><kwd>carrier erythrocyte</kwd><kwd>drug delivery</kwd><kwd>enzyme replacement therapy</kwd><kwd>erythrocyte-bioreactor</kwd><kwd>targeted drug delivery</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>доставка лекарств</kwd><kwd>эритроцит-носитель</kwd><kwd>направленная доставка лекарств</kwd><kwd>эритроцит-биореактор</kwd><kwd>противоопухолевая терапия</kwd><kwd>фермент-заместительная терапия</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа поддержана грантом Российского фонда фундаментальных исследований для аспирантов второго года №19‐34‐90035 (для Колевой Л.Д.), а также Министерством науки и высшего образования РФ (проекты AAAA‐A17‐117112420087‐0 и AAAA‐A19‐119111690006‐9).</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">1. Атауллаханов Ф.И., Борсакова Д.В., Протасов Е.С., Синауридзе Е.И., Зейналов А.М. Эритроцит: мешок с гемоглобином или живая, активная клетка? Вопросы гематологии/онкологии и иммунопатологии в педиатрии 2018; 17 (1): 108–16.</mixed-citation><mixed-citation xml:lang="ru">Атауллаханов Ф.И., Борсакова Д.В., Протасов Е.С., Синауридзе Е.И., Зейналов А.М. Эритроцит: мешок с гемоглобином или живая, активная клетка? Вопросы гематологии/онкологии и иммунопатологии в педиатрии 2018; 17 (1): 108–16.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Koleva L., Bovt E., Ataullakhanov F., Sinauridze E. Erythrocytes as carriers : from drug delivery to biosensors. Pharmaceutics 2020; 12 (3): 276.</mixed-citation><mixed-citation xml:lang="ru">Koleva L., Bovt E., Ataullakhanov F., Sinauridze E. Erythrocytes as carriers : from drug delivery to biosensors. Pharmaceutics 2020; 12 (3): 276.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Pierigè F., Bigini N., Rossi L., Magnani M. Reengineering red blood cells for cellular therapeutics and diagnostics. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2017; 9 (5): e1454. DOI: 10.1002/wnan.1454</mixed-citation><mixed-citation xml:lang="ru">Pierigè F., Bigini N., Rossi L., Magnani M. Reengineering red blood cells for cellular therapeutics and diagnostics. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2017; 9 (5): e1454. DOI: 10.1002/wnan.1454</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. Fernandes H.S., Silva Teixeira C.S., Fernandes P.A., Ramos M.J., Cerqueira N.M.F.S.A. Amino acid deprivation using enzymes as a targeted therapy for cancer and viral infections. Expert Opin Ther Pat 2017; 27 (3): 283–97.</mixed-citation><mixed-citation xml:lang="ru">Fernandes H.S., Silva Teixeira C.S., Fernandes P.A., Ramos M.J., Cerqueira N.M.F.S.A. Amino acid deprivation using enzymes as a targeted therapy for cancer and viral infections. Expert Opin Ther Pat 2017; 27 (3): 283–97.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Rytting M.E. Role of L-asparaginase in acute lymphoblastic leukemia: focus on adult patients. Blood Lymphat Cancer Targets Ther 2012; 2: 117–24.</mixed-citation><mixed-citation xml:lang="ru">Rytting M.E. Role of L-asparaginase in acute lymphoblastic leukemia: focus on adult patients. Blood Lymphat Cancer Targets Ther 2012; 2: 117–24.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Cremel M., Guerin N., Campello G., Barthe Q., Berlier W., Horand F., et al. Innovative approach in Pompe disease therapy: induction of immune tolerance by antigen-encapsulated red blood cells. Int J Pharm 2015; 491 (1–2): 69–77.</mixed-citation><mixed-citation xml:lang="ru">Cremel M., Guerin N., Campello G., Barthe Q., Berlier W., Horand F., et al. Innovative approach in Pompe disease therapy: induction of immune tolerance by antigen-encapsulated red blood cells. Int J Pharm 2015; 491 (1–2): 69–77.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Minetto P., Bisso N., Guolo F., Clavio M., Coviello E., Guardo D., et al. Patient and therapy-related factors affecting the toxicity of pegylated-asparaginase for the treatment of adult acute lymphoblastic leukemia. Blood 2017; 130 (Suppl 1): 1297.</mixed-citation><mixed-citation xml:lang="ru">Minetto P., Bisso N., Guolo F., Clavio M., Coviello E., Guardo D., et al. Patient and therapy-related factors affecting the toxicity of pegylated-asparaginase for the treatment of adult acute lymphoblastic leukemia. Blood 2017; 130 (Suppl 1): 1297.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Booth C., Gaspar B. Pegademase bovine (PEG-ADA) for the treatment of infants and children with severe combined immunodeficiency (SCID). Biologics 2009; 3: 349–58.</mixed-citation><mixed-citation xml:lang="ru">Booth C., Gaspar B. Pegademase bovine (PEG-ADA) for the treatment of infants and children with severe combined immunodeficiency (SCID). Biologics 2009; 3: 349–58.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Bax B.E., Bain M.D., Fairbanks L.D., Chalmers R.A., Webster A.D.B. In vitro and in vivo studies with human carrier erythrocytes loaded with polyethylene glycol-conjugated and native adenosine deaminase. Br J Haematol 2000; 109 (3): 549–54.</mixed-citation><mixed-citation xml:lang="ru">Bax B.E., Bain M.D., Fairbanks L.D., Chalmers R.A., Webster A.D.B. In vitro and in vivo studies with human carrier erythrocytes loaded with polyethylene glycol-conjugated and native adenosine deaminase. Br J Haematol 2000; 109 (3): 549–54.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Levene M., Bain M., Moran N., Nirmalananthan N., Poulton J., Scarpelli M., et al. Safety and efficacy of erythrocyte encapsulated thymidine phosphorylase in mitochondrial neurogastrointestinal encephalomyopathy. J Clin Med 2019; 8 (4): 457.</mixed-citation><mixed-citation xml:lang="ru">Levene M., Bain M., Moran N., Nirmalananthan N., Poulton J., Scarpelli M., et al. Safety and efficacy of erythrocyte encapsulated thymidine phosphorylase in mitochondrial neurogastrointestinal encephalomyopathy. J Clin Med 2019; 8 (4): 457.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Halfon-Domenech C., Thomas X., Chabaud S., Baruchel A., Gueyffier F., Mazingue F., et al. l-asparaginase loaded red blood cells in refractory or relapsing acute lymphoblastic leukaemia in children and adults: Results of the GRASPALL 2005-01 randomized trial. Br J Haematol 2011; 153 (1): 58–65.</mixed-citation><mixed-citation xml:lang="ru">Halfon-Domenech C., Thomas X., Chabaud S., Baruchel A., Gueyffier F., Mazingue F., et al. l-asparaginase loaded red blood cells in refractory or relapsing acute lymphoblastic leukaemia in children and adults: Results of the GRASPALL 2005-01 randomized trial. Br J Haematol 2011; 153 (1): 58–65.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Hunault-Berger M., Leguay T., Huguet F., Leprêtre S., Deconinck E., Ojeda-Uribe M., et al. A Phase 2 study of L-asparaginase encapsulated in erythrocytes in elderly patients with Philadelphia chromosome negative acute lymphoblastic leukemia: The GRASPALL/GRAALL-SA2-2008 study. Am J Hematol 2015; 90 (9): 811–8.</mixed-citation><mixed-citation xml:lang="ru">Hunault-Berger M., Leguay T., Huguet F., Leprêtre S., Deconinck E., Ojeda-Uribe M., et al. A Phase 2 study of L-asparaginase encapsulated in erythrocytes in elderly patients with Philadelphia chromosome negative acute lymphoblastic leukemia: The GRASPALL/GRAALL-SA2-2008 study. Am J Hematol 2015; 90 (9): 811–8.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Bax B.E., Bain M.D., Fairbanks L.D., Simmonds H.A., Webster A.D., Ronald A. Carrier erythrocyte entrapped adenosine deaminase therapy in adenosine deaminase deficiency. Adv Exp Med Biol 2000; 486: 47–50.</mixed-citation><mixed-citation xml:lang="ru">Bax B.E., Bain M.D., Fairbanks L.D., Simmonds H.A., Webster A.D., Ronald A. Carrier erythrocyte entrapped adenosine deaminase therapy in adenosine deaminase deficiency. Adv Exp Med Biol 2000; 486: 47–50.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Bax B.E., Bain M.D., Fairbanks L.D., Webster A.D.B., Ind P.W., Hershfield M.S., et al. A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency. Eur J Haematol 2007; 79 (4): 338–48. DOI: 10.1111/j.1600-0609.2007.00927.x</mixed-citation><mixed-citation xml:lang="ru">Bax B.E., Bain M.D., Fairbanks L.D., Webster A.D.B., Ind P.W., Hershfield M.S., et al. A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency. Eur J Haematol 2007; 79 (4): 338–48. DOI: 10.1111/j.1600-0609.2007.00927.x</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Filosto M., Piccinelli S.C., Caria F., Cassarino S.G., Baldelli E., Galvagni A., et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE-MTDPS1). J Clin Med 2018; 7 (11): 389. DOI: 10.3390/jcm7110389</mixed-citation><mixed-citation xml:lang="ru">Filosto M., Piccinelli S.C., Caria F., Cassarino S.G., Baldelli E., Galvagni A., et al. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE-MTDPS1). J Clin Med 2018; 7 (11): 389. DOI: 10.3390/jcm7110389</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Halter J., Schupbach W., Casali C., Elhasid R., Fay K., Hammans S., et al. Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach. Bone Marrow Transplant 2011; 46 (3): 330–7.</mixed-citation><mixed-citation xml:lang="ru">Halter J., Schupbach W., Casali C., Elhasid R., Fay K., Hammans S., et al. Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach. Bone Marrow Transplant 2011; 46 (3): 330–7.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Baruchel A., Bertrand Y., Thomas X., Blin N., Tavernier E., Ducassou S., et al. Updated clinical activity of GRASPA versus native l-asparaginase in combination with cooprall regimen in phase 3 randomized trial in patients with relapsed acute lymphoblastic leukemia. Blood 2015; 126 (23): 3723.</mixed-citation><mixed-citation xml:lang="ru">Baruchel A., Bertrand Y., Thomas X., Blin N., Tavernier E., Ducassou S., et al. Updated clinical activity of GRASPA versus native l-asparaginase in combination with cooprall regimen in phase 3 randomized trial in patients with relapsed acute lymphoblastic leukemia. Blood 2015; 126 (23): 3723.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Bachet J., Gay F., Maréchal R., Galais M., Adenis A., Salako D., et al. Asparagine synthetase expression and phase I study with L -asparaginase encapsulated in red blood cells in patients with pancreatic adenocarcinoma. Pancreas 2015; 44 (7): 1141–7.</mixed-citation><mixed-citation xml:lang="ru">Bachet J., Gay F., Maréchal R., Galais M., Adenis A., Salako D., et al. Asparagine synthetase expression and phase I study with L -asparaginase encapsulated in red blood cells in patients with pancreatic adenocarcinoma. Pancreas 2015; 44 (7): 1141–7.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Hammel P., Bachet J.-B., Portales F., Mineur L., Metges J.-P., de la Fouchardiere C., et al. 621PDA Phase 2b of eryaspase in combination with gemcitabine or FOLFOX as second-line therapy in patients with metastatic pancreatic adenocarcinoma (NCT02195180). Ann Oncol 2017.</mixed-citation><mixed-citation xml:lang="ru">Hammel P., Bachet J.-B., Portales F., Mineur L., Metges J.-P., de la Fouchardiere C., et al. 621PDA Phase 2b of eryaspase in combination with gemcitabine or FOLFOX as second-line therapy in patients with metastatic pancreatic adenocarcinoma (NCT02195180). Ann Oncol 2017.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Gay F., Aguera K., Sénéchal K., Tainturier A., Berlier W., Maucort-Boulch D., et al. Methionine tumor starvation by erythrocyte-encapsulated methionine gamma-lyase activity controlled with per os vitamin B6. Cancer Med 2017; 6 (6): 1437–52.</mixed-citation><mixed-citation xml:lang="ru">Gay F., Aguera K., Sénéchal K., Tainturier A., Berlier W., Maucort-Boulch D., et al. Methionine tumor starvation by erythrocyte-encapsulated methionine gamma-lyase activity controlled with per os vitamin B6. Cancer Med 2017; 6 (6): 1437–52.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Sénéchal K., Maubant S., Leblanc M., Ciré S., Gallix F., Andrivon A., et al. Erymethionase (methionine-gamma-lyase encapsulated into red blood cells) potentiates anti-PD-1 therapy in TNBC syngeneic mouse model [abstract]. Proc Am Assoc Cancer Res Annu Meet 2019; 2019 Mar 29–Apr 3; Atlanta, GA Philadelphia AACR. Cancer Res 2019; 79 (13 Suppl): Abstract nr 2258.</mixed-citation><mixed-citation xml:lang="ru">Sénéchal K., Maubant S., Leblanc M., Ciré S., Gallix F., Andrivon A., et al. Erymethionase (methionine-gamma-lyase encapsulated into red blood cells) potentiates anti-PD-1 therapy in TNBC syngeneic mouse model [abstract]. Proc Am Assoc Cancer Res Annu Meet 2019; 2019 Mar 29–Apr 3; Atlanta, GA Philadelphia AACR. Cancer Res 2019; 79 (13 Suppl): Abstract nr 2258.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">22. Gay F., Aguera K., Senechal K., Bes J., Chevrier A.-M., Gallix F., et al. Arginine deiminase loaded in erythrocytes: a promising formulation for L-arginine deprivation therapy in cancers. [abstract]. Proc 107th Annu Meet Am Assoc Cancer Res 2016 Apr 16–20; New Orleans, LA Philadelphia AACR. Cancer Res 2016; 76 (14 Suppl): Abstract nr 4812.</mixed-citation><mixed-citation xml:lang="ru">Gay F., Aguera K., Senechal K., Bes J., Chevrier A.-M., Gallix F., et al. Arginine deiminase loaded in erythrocytes: a promising formulation for L-arginine deprivation therapy in cancers. [abstract]. Proc 107th Annu Meet Am Assoc Cancer Res 2016 Apr 16–20; New Orleans, LA Philadelphia AACR. Cancer Res 2016; 76 (14 Suppl): Abstract nr 4812.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">23. Yuan S.H., Ge W.H., Huo J., Wang X.H. Slow release properties and liver-targeting characteristics of methotrexate erythrocyte carriers. Fundam Clin Pharmacol 2009; 23 (2): 189–96.</mixed-citation><mixed-citation xml:lang="ru">Yuan S.H., Ge W.H., Huo J., Wang X.H. Slow release properties and liver-targeting characteristics of methotrexate erythrocyte carriers. Fundam Clin Pharmacol 2009; 23 (2): 189–96.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">24. Rossi L., Castro M., D’Orio F., Damonte G., Serafini S., Bigi L., et al. Low doses of dexamethasone constantly delivered by autologous erythrocytes slow the progression of lung disease in cystic fibrosis patients. Blood Cells Mol Dis 2004; 33 (1): 57–63.</mixed-citation><mixed-citation xml:lang="ru">Rossi L., Castro M., D’Orio F., Damonte G., Serafini S., Bigi L., et al. Low doses of dexamethasone constantly delivered by autologous erythrocytes slow the progression of lung disease in cystic fibrosis patients. Blood Cells Mol Dis 2004; 33 (1): 57–63.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">25. Bossa F., Latiano A., Rossi L., Magnani M., Palmieri O., Dallapiccola B., et al. Erythrocyte-mediated delivery of dexamethasone in patients with mild-to-moderate ulcerative colitis, refractory to mesalamine: A randomized, controlled study. Am J Gastroenterol 2008; 103 (10): 2509–16.</mixed-citation><mixed-citation xml:lang="ru">Bossa F., Latiano A., Rossi L., Magnani M., Palmieri O., Dallapiccola B., et al. Erythrocyte-mediated delivery of dexamethasone in patients with mild-to-moderate ulcerative colitis, refractory to mesalamine: A randomized, controlled study. Am J Gastroenterol 2008; 103 (10): 2509–16.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">26. Castro M., Rossi L., Papadatou B., Bracci F., Knafelz D., Ambrosini M., et al. Longterm treatment with autologous red blood cells loaded with dexamethasone 21–phosphate in pediatric patients affected by steroid-dependent Crohn disease. J Pediatr Gastroenterol Nutr 2007; 44: 423–6.</mixed-citation><mixed-citation xml:lang="ru">Castro M., Rossi L., Papadatou B., Bracci F., Knafelz D., Ambrosini M., et al. Longterm treatment with autologous red blood cells loaded with dexamethasone 21–phosphate in pediatric patients affected by steroid-dependent Crohn disease. J Pediatr Gastroenterol Nutr 2007; 44: 423–6.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">27. Skorokhod O.A., Kulikova E.V., Galkina N.M., Medvedev P.V., Zybunova E.E., Vitvitsky V.M., et al. Doxorubicin pharmacokinetics in lymphoma patients treated with doxorubicin-loaded eythrocytes. Haematologica 2007; 92 (4): 570–1.</mixed-citation><mixed-citation xml:lang="ru">Skorokhod O.A., Kulikova E.V., Galkina N.M., Medvedev P.V., Zybunova E.E., Vitvitsky V.M., et al. Doxorubicin pharmacokinetics in lymphoma patients treated with doxorubicin-loaded eythrocytes. Haematologica 2007; 92 (4): 570–1.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">28. Skorokhod O.A., Garmaeva T., Vitvitsky V.M., Isaev V.G., Parovichnikova E.N., Savchenko V.G., et al. Pharmacokinetics of erythrocyte-bound daunorubicin in patients with acute leukemia. Med Sci Monit 2004; 10 (4): 55–64.</mixed-citation><mixed-citation xml:lang="ru">Skorokhod O.A., Garmaeva T., Vitvitsky V.M., Isaev V.G., Parovichnikova E.N., Savchenko V.G., et al. Pharmacokinetics of erythrocyte-bound daunorubicin in patients with acute leukemia. Med Sci Monit 2004; 10 (4): 55–64.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">29. Sawyer D.B., Peng X., Chen B., Pentassuglia L., Lim C.C. Mechanisms of anthracycline cardiac injury: can we identify strategies for cardioprotection? Prog Cardiovasc Dis 2010; 53 (2): 105–13.</mixed-citation><mixed-citation xml:lang="ru">Sawyer D.B., Peng X., Chen B., Pentassuglia L., Lim C.C. Mechanisms of anthracycline cardiac injury: can we identify strategies for cardioprotection? Prog Cardiovasc Dis 2010; 53 (2): 105–13.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">30. Czock D., Keller F., Rasche F.M., Ulla H. Pharmacokinetics and pharmacodynamics of systemically administered glucocorticoids. Clin Pharmacokinet 2005; 44 (1): 61–98.</mixed-citation><mixed-citation xml:lang="ru">Czock D., Keller F., Rasche F.M., Ulla H. Pharmacokinetics and pharmacodynamics of systemically administered glucocorticoids. Clin Pharmacokinet 2005; 44 (1): 61–98.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">31. Ataullakhanov F.I., Isaev V.G., Kohno A.V., Kulikova E.V., Parovichnikova E.N., Savchenko V.G., et al. Pharmacokinetics of doxorubicin in patients with lymphoproliferative disorders after infusion of doxorubicin-loaded erythrocytes. In: Sprandel U., Way J.L. (ed.). Erythrocytes as Drug Carriers in Medicine. Boston, MA: Springer US; 1997. Рp. 137–142.</mixed-citation><mixed-citation xml:lang="ru">Ataullakhanov F.I., Isaev V.G., Kohno A.V., Kulikova E.V., Parovichnikova E.N., Savchenko V.G., et al. Pharmacokinetics of doxorubicin in patients with lymphoproliferative disorders after infusion of doxorubicin-loaded erythrocytes. In: Sprandel U., Way J.L. (ed.). Erythrocytes as Drug Carriers in Medicine. Boston, MA: Springer US; 1997. Рp. 137–142.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">32. Murciano J., Medinilla S., Eslin D., Atochina E., Cines D.B., Muzykantov V.R. Prophylactic fibrinolysis through selective dissolution of nascent clots by tPA-carrying erythrocytes. Nat Biotechnol 2003; 21 (8): 891–6.</mixed-citation><mixed-citation xml:lang="ru">Murciano J., Medinilla S., Eslin D., Atochina E., Cines D.B., Muzykantov V.R. Prophylactic fibrinolysis through selective dissolution of nascent clots by tPA-carrying erythrocytes. Nat Biotechnol 2003; 21 (8): 891–6.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">33. Stein S.C., Ganguly K., Belfield C.M., Xu X., Swanson E.W., Chen X.-H., et al. Erythrocyte-bound tissue plasminogen activator is neuroprotective in experimental traumatic brain injury. J Neurotrauma 2009; 26 (9): 1585–92.</mixed-citation><mixed-citation xml:lang="ru">Stein S.C., Ganguly K., Belfield C.M., Xu X., Swanson E.W., Chen X.-H., et al. Erythrocyte-bound tissue plasminogen activator is neuroprotective in experimental traumatic brain injury. J Neurotrauma 2009; 26 (9): 1585–92.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">34. Armstead W.M., Ganguly K., Riley J., Kiessling W.J., Cines D.B., Higazi A.A.R., et al. Red blood cell-coupled tissue plasminogen activator prevents impairment of cerebral vasodilatory responses through inhibition of c-Jun-N-terminal kinase and potentiation of p38 mitogen-activated protein kinase after cerebral photothrombosis in the newborn. Pediatr Crit Care Med 2011; 12 (6): e369.</mixed-citation><mixed-citation xml:lang="ru">Armstead W.M., Ganguly K., Riley J., Kiessling W.J., Cines D.B., Higazi A.A.R., et al. Red blood cell-coupled tissue plasminogen activator prevents impairment of cerebral vasodilatory responses through inhibition of c-Jun-N-terminal kinase and potentiation of p38 mitogen-activated protein kinase after cerebral photothrombosis in the newborn. Pediatr Crit Care Med 2011; 12 (6): e369.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">35. Muzykantov V.R., Murciano J.C., Taylor R.P., Atochina E.N., Herraez A. Regulation of the complement-mediated elimination of red blood cells modified with biotin and streptavidin. Anal Biochem 1996; 241 (1): 109–19.</mixed-citation><mixed-citation xml:lang="ru">Muzykantov V.R., Murciano J.C., Taylor R.P., Atochina E.N., Herraez A. Regulation of the complement-mediated elimination of red blood cells modified with biotin and streptavidin. Anal Biochem 1996; 241 (1): 109–19.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">36. Muzykantov V.R., Barnathan E.S., Atochina E.N., Kuo A., Danilov S.M., Fisher A.B. Targeting of antibody-conjugated plasminogen activators to the pulmonary vasculature. J Pharmacol Exp Ther. 1996;279(2):1026–34.</mixed-citation><mixed-citation xml:lang="ru">Muzykantov V.R., Barnathan E.S., Atochina E.N., Kuo A., Danilov S.M., Fisher A.B. Targeting of antibody-conjugated plasminogen activators to the pulmonary vasculature. J Pharmacol Exp Ther. 1996;279(2):1026–34.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">37. Pozzi L.-A.M., Maciaszek J.W., Rock K.L. Both dendritic cells and macrophages can stimulate naive CD8 T cells in vivo to proliferate, develop effector function, and differentiate into memory cells. J Immunol 2005; 175 (4): 2071–81.</mixed-citation><mixed-citation xml:lang="ru">Pozzi L.-A.M., Maciaszek J.W., Rock K.L. Both dendritic cells and macrophages can stimulate naive CD8 T cells in vivo to proliferate, develop effector function, and differentiate into memory cells. J Immunol 2005; 175 (4): 2071–81.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">38. Eichler H.G., Gasic S., Bauer K., Korn A., Bacher S. In vivo clearance of antibody-sensitized human drug carrier erythrocytes. Drug-carrier erythrocytes. 1986;40(3):300–3. Clin Pharmacol Ther 1986; 40 (3): 300-3. DOI: 10.1038/clpt.1986.180</mixed-citation><mixed-citation xml:lang="ru">Eichler H.G., Gasic S., Bauer K., Korn A., Bacher S. In vivo clearance of antibody-sensitized human drug carrier erythrocytes. Drug-carrier erythrocytes. 1986;40(3):300–3. Clin Pharmacol Ther 1986; 40 (3): 300-3. DOI: 10.1038/clpt.1986.180</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">39. Delaby C., Pilard N., Hetet G., Driss F., Grandchamp B., Beaumont C., Canonne-Hergaux F. A physiological model to study iron recycling in macrophages. Exp Cell Res 2005; 310 (1): 43–53.</mixed-citation><mixed-citation xml:lang="ru">Delaby C., Pilard N., Hetet G., Driss F., Grandchamp B., Beaumont C., Canonne-Hergaux F. A physiological model to study iron recycling in macrophages. Exp Cell Res 2005; 310 (1): 43–53.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">40. DeLoach J.R., Tangner C.H., Barton C. Hepatic pharmacokinetics of glutaraldehyde-treated methotrexate-loaded carrier erythrocytes in dogs. Res Exp Med 1983; 183 (3): 167–75.</mixed-citation><mixed-citation xml:lang="ru">DeLoach J.R., Tangner C.H., Barton C. Hepatic pharmacokinetics of glutaraldehyde-treated methotrexate-loaded carrier erythrocytes in dogs. Res Exp Med 1983; 183 (3): 167–75.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">41. Bratosin D., Mazurier J., Tissier J.P., Slomianny C., Estaquier J., Russo-Marie F., et al. Molecular mechanisms of erythrophagocytosis. Characterization of the senescent erythrocytes that are phagocytized by macrophages. C R Acad Sci III. 1997; 320 (10): 811–8. DOI: 10.1016/s0764-4469(97)85017-2</mixed-citation><mixed-citation xml:lang="ru">Bratosin D., Mazurier J., Tissier J.P., Slomianny C., Estaquier J., Russo-Marie F., et al. Molecular mechanisms of erythrophagocytosis. Characterization of the senescent erythrocytes that are phagocytized by macrophages. C R Acad Sci III. 1997; 320 (10): 811–8. DOI: 10.1016/s0764-4469(97)85017-2</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">42. Mishra P.R., Jain N.K. Biotinylated methotrexate loaded erythrocytes for enhanced liver uptake. “A study on the rat”. Int J Pharm 2002; 231 (2): 145–53. DOI: 10.1016/s0378-5173(01)00847-x</mixed-citation><mixed-citation xml:lang="ru">Mishra P.R., Jain N.K. Biotinylated methotrexate loaded erythrocytes for enhanced liver uptake. “A study on the rat”. Int J Pharm 2002; 231 (2): 145–53. DOI: 10.1016/s0378-5173(01)00847-x</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">43. Magnani M., Rossi L., Fraternale A., Casabianca A., Brandi G., Benatti U., De Flora A. Targeting antiviral nucleotide analogues to macrophages. J Leukoc Biol 1997; 62 (1): 133–7.</mixed-citation><mixed-citation xml:lang="ru">Magnani M., Rossi L., Fraternale A., Casabianca A., Brandi G., Benatti U., De Flora A. Targeting antiviral nucleotide analogues to macrophages. J Leukoc Biol 1997; 62 (1): 133–7.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">44. Magnani M., Rossi L., Fraternale A., Silvotti L., Quintavalla F., Piedimonte G., et al. FIV infection of macrophages: in vitro and in vivo inhibition by dideoxycytidine 5′-triphosphate. Vet Immunol Immunopathol 1995; 46 (1): 151–8.</mixed-citation><mixed-citation xml:lang="ru">Magnani M., Rossi L., Fraternale A., Silvotti L., Quintavalla F., Piedimonte G., et al. FIV infection of macrophages: in vitro and in vivo inhibition by dideoxycytidine 5′-triphosphate. Vet Immunol Immunopathol 1995; 46 (1): 151–8.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">45. Magnani M., Balestra E., Fraternale A., Aquaro S., Paiardini M., Cervasi B., et al. Drug-loaded red blood cell-mediated clearance of HIV-1 macrophage reservoir by selective inhibition of STAT1 expression. J Leukoc Biol 2003; 74 (5): 764–71.</mixed-citation><mixed-citation xml:lang="ru">Magnani M., Balestra E., Fraternale A., Aquaro S., Paiardini M., Cervasi B., et al. Drug-loaded red blood cell-mediated clearance of HIV-1 macrophage reservoir by selective inhibition of STAT1 expression. J Leukoc Biol 2003; 74 (5): 764–71.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">46. Dominici S., Laguardia M.E., Serafini G., Chiarantini L., Fortini C., Tripiciano A., et al. Red blood cell-mediated delivery of recombinant HIV-1 Tat protein in mice induces anti-Tat neutralizing antibodies and CTL. Vaccine. 2003; 21: 2082–90.</mixed-citation><mixed-citation xml:lang="ru">Dominici S., Laguardia M.E., Serafini G., Chiarantini L., Fortini C., Tripiciano A., et al. Red blood cell-mediated delivery of recombinant HIV-1 Tat protein in mice induces anti-Tat neutralizing antibodies and CTL. Vaccine. 2003; 21: 2082–90.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">47. Franco R., Dufour E., Kosenko E., Bax B.E., Banz A., Skorokhod O.A., et al. International seminar on the red blood cells as vehicles for drugs. Expert Opin Biol Ther 2012; 12 (1): 127–33.</mixed-citation><mixed-citation xml:lang="ru">Franco R., Dufour E., Kosenko E., Bax B.E., Banz A., Skorokhod O.A., et al. International seminar on the red blood cells as vehicles for drugs. Expert Opin Biol Ther 2012; 12 (1): 127–33.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">48. Sabatino R., Antonelli A., Battistelli S., Schwendener R., Magnani M., Rossi L. Macrophage depletion by free bisphosphonates and zoledronate-loaded red blood cells. PLoS One 2014; 9 (6): e101260.</mixed-citation><mixed-citation xml:lang="ru">Sabatino R., Antonelli A., Battistelli S., Schwendener R., Magnani M., Rossi L. Macrophage depletion by free bisphosphonates and zoledronate-loaded red blood cells. PLoS One 2014; 9 (6): e101260.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">49. Mishra P.R., Jain N.K. Surface modified methotrexate loaded erythrocytes for enhanced macrophage uptake. J Drug Target 2000; 8 (4): 217–24.</mixed-citation><mixed-citation xml:lang="ru">Mishra P.R., Jain N.K. Surface modified methotrexate loaded erythrocytes for enhanced macrophage uptake. J Drug Target 2000; 8 (4): 217–24.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">50. Cremel M., Guérin N., Horand F., Banz A., Godfrin Y. Red blood cells as innovative antigen carrier to induce specific immune tolerance. Int J Pharm 2013; 443 (1–2): 39–49.</mixed-citation><mixed-citation xml:lang="ru">Cremel M., Guérin N., Horand F., Banz A., Godfrin Y. Red blood cells as innovative antigen carrier to induce specific immune tolerance. Int J Pharm 2013; 443 (1–2): 39–49.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">51. Magnani M., Chiarantini L., Vittoria E., Mancini U., Rossi L., Fazi A. Red blood cells as an antigen-delivery system. Biotechnol Appl Biochem 1992; 16 (2): 188– 94.</mixed-citation><mixed-citation xml:lang="ru">Magnani M., Chiarantini L., Vittoria E., Mancini U., Rossi L., Fazi A. Red blood cells as an antigen-delivery system. Biotechnol Appl Biochem 1992; 16 (2): 188– 94.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">52. Chiarantini L., Argnanit R., Zucchinit S., Stevanatot L., Grossi M.P., Magnani M., et al. Red blood cells as delivery system for recombinant HSV-1 glycoprotein B: immunogenicity and protection in mice. Vaccine 1997; 15 (3): 276–80.</mixed-citation><mixed-citation xml:lang="ru">Chiarantini L., Argnanit R., Zucchinit S., Stevanatot L., Grossi M.P., Magnani M., et al. Red blood cells as delivery system for recombinant HSV-1 glycoprotein B: immunogenicity and protection in mice. Vaccine 1997; 15 (3): 276–80.</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">53. Banz A., Cremel M., Mouvant A., Guerin N., Horand F., Godfrin Y. Tumor growth control using red blood cells as the antigen delivery system and poly (I: C). J Immunother 2012; 35 (5): 409–17.</mixed-citation><mixed-citation xml:lang="ru">Banz A., Cremel M., Mouvant A., Guerin N., Horand F., Godfrin Y. Tumor growth control using red blood cells as the antigen delivery system and poly (I: C). J Immunother 2012; 35 (5): 409–17.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">54. Banz A., Cremel M., Rembert A., Godfrin Y. In situ targeting of dendritic cells by antigen-loaded red blood cells: A novel approach to cancer immunotherapy. Vaccine 2010; 28 (17): 2965–72.</mixed-citation><mixed-citation xml:lang="ru">Banz A., Cremel M., Rembert A., Godfrin Y. In situ targeting of dendritic cells by antigen-loaded red blood cells: A novel approach to cancer immunotherapy. Vaccine 2010; 28 (17): 2965–72.</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">55. Renno T., Lebecque S., Renard N., Saeland S., Vicari A. What’s new in the field of cancer vaccines? Cell Mol Life Sci 2003; 60 (7): 1296–310.</mixed-citation><mixed-citation xml:lang="ru">Renno T., Lebecque S., Renard N., Saeland S., Vicari A. What’s new in the field of cancer vaccines? Cell Mol Life Sci 2003; 60 (7): 1296–310.</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">56. Pipeline Erytech. [Электронный оесурс]. URL: https://erytech.com/pipeline/ (Дата обращения 28.11.2020)</mixed-citation><mixed-citation xml:lang="ru">Pipeline Erytech. [Электронный оесурс]. URL: https://erytech.com/pipeline/ (Дата обращения 28.11.2020)</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">57. European Medical Agency [Электронный ресурс]. URL: https://www.ema.europa.eu/en. (Дата обращения 28.11.2020)</mixed-citation><mixed-citation xml:lang="ru">European Medical Agency [Электронный ресурс]. URL: https://www.ema.europa.eu/en. (Дата обращения 28.11.2020)</mixed-citation></citation-alternatives></ref></ref-list></back></article>
