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<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">158</article-id><article-id pub-id-type="doi">10.24287/1726-1708-2016-15-2-27-31</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Pathogen inactivation technologies and quality of platelet concentrates (Review of literature)</article-title><trans-title-group xml:lang="ru"><trans-title>Технологии инактивации патогенов и качество концентратов тромбоцитов (обзор литературы)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ignatova</surname><given-names>Anastasia A.</given-names></name><name xml:lang="ru"><surname>Игнатова</surname><given-names>Анастасия Александровна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>procyonnlotor@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Trakhtman</surname><given-names>Pavel E.</given-names></name><name xml:lang="ru"><surname>Трахтман</surname><given-names>Павел Евгеньевич</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>trakhtman@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Panteleev</surname><given-names>Mikhail A.</given-names></name><name xml:lang="ru"><surname>Пантелеев</surname><given-names>Михаил Александрович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>mapanteleev@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Federal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitry Rogachev, Ministry of Health of the Russian Federation</institution></aff><aff><institution xml:lang="ru">Федеральный научно-клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2016-06-19" publication-format="electronic"><day>19</day><month>06</month><year>2016</year></pub-date><volume>15</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>27</fpage><lpage>31</lpage><history><date date-type="received" iso-8601-date="2018-09-19"><day>19</day><month>09</month><year>2018</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2016, «D. Rogachev NMRCPHOI»</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2016, ФГБУ «НМИЦ ДГОИ им. Дмитрия Рогачева» Минздрава России</copyright-statement><copyright-year>2016</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/158">https://hemoncim.com/jour/article/view/158</self-uri><abstract xml:lang="en"><p>Platelet concentrate (PC) transfusion is practically the only fast and universal way of correcting platelet function in a broad range of clinical situations in paediatric haematology. Due to a short storage time of PC, technologies of pathogen inactivation are very important for decreasing the risks of immune responses and infections. There are numerous studies indicating that platelet function can change in pathogen inactivation. The article offers a literature review of laboratory and clinical studies aimed at assessment of the significance and direction of these changes, and also discusses practical implications of such studies for clinical work with PC.</p></abstract><trans-abstract xml:lang="ru"><p>Переливание концентратов тромбоцитов (КТ) является практически единственным быстрым и универсальным способом коррекции тромбоцитарной функции при широком спектре клинических ситуаций в детской гематологии. В силу короткого срока хранения КТ технологии инактивации патогенов крайне важны для снижения рисков иммунных реакций и инфекций. Однако существует большое количество исследований, свидетельствующих о том, что функция тромбоцитов при инактивации патогенов может меняться. В обзоре литературы рассмотрены лабораторные и клинические исследования, направленные на оценку значимости и направленности этих изменений, а также обсуждено практическое значение этих исследований для клинической работы с КТ.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>технологии инактивации патогенов</kwd><kwd>тромбоциты</kwd><kwd>функциональная активность тромбоцитов</kwd><kwd>pathogen inactivation technologies</kwd><kwd>platelets</kwd><kwd>platelet functional activity</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Атауллаханов ФИ, Воробьев АИ, Емельяненко ВМ, Пантелеев МА. Искусственные и лиофилизированные тромбоциты: реальная альтернатива тромбоконцентратам? Гематология и трансфузиология. 2010;55(5):14-9</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Kaiser-Guignard J, Canellini G, Lion N, Abonnenc M, Osselaer JC, Tissot JD. The clinical and biological impact of new pathogen inactivation technologies on platelet concentrates. Blood Rev. 2014;28(6):235-41.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Marschner S, Goodrich R. Pathogen reduction technology treatment of platelets, plasma and whole blood using riboflavin and UV light. Transfus Med Hemother. 2011;38(1):8-18.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lin L, Dikeman R, Molini B, Lukehart SA, Lane R, Dupuis K, et al. Photochemical treatment of platelet concentrates with amotosalen and long-wavelength ultraviolet light inactivates a broad spectrum of pathogenic bacteria. Transfusion. 2004;44(10):1496-504.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Seghatchian J, Tolksdorf F. Characteristics of the THERAFLEX UV-Platelets pathogen inactivation system - an update. Transfus Apher Sci. 2012;46(2):221-9.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>van Rhenen DJ, Vermeij J, Mayaudon V, Hind C, Lin L, Corash L. Functional characteristics of S-59 photochemically treated platelet concentrates derived from buffy coats. Vox Sang. 2000;79(4):206-14.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Picker SM, Speer R, Gathof BS. Functional characteristics of buffy-coat PLTs photochemically treated with amotosalen-HCl for pathogen inactivation. Transfusion. 2004;44(3):320-9.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>AuBuchon JP, Herschel L, Roger J, Taylor H, Whitley P, Li J, et al. Efficacy of apheresis platelets treated with riboflavin and ultraviolet light for pathogen reduction. Transfusion. 2005;45(8):1335-41.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Johnson L, Loh YS, Kwok M, Marks DC. In vitro assessment of buffy-coat derived platelet components suspended in SSP+ treated with the INTERCEPT Blood system. Transfusion Med. 2013;23(2):121-9.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Carvalho H, Alguero C, Santos M, de Sousa G, Trindade H, Seghatchian J. The combined effect of platelet storage media and intercept pathogen reduction technology on platelet activation/activability and cellular apoptosis/necrosis: Lisbon-RBS experience. Transfus Apher Sci. 2006;34(2):187-92.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Apelseth T0, Bruserud 0, Wentzel-Larsen T, Bakken AM, Bj0rsvik S, Hervig T. In vitro evaluation of metabolic changes and residual platelet responsiveness in photochemical treated and gamma-irradiated single-donor platelet concentrates during long-term storage. Transfusion. 2007;47(4):653-65.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Middelburg RA, Roest M, Ham J, Coccoris M, Zwaginga JJ, van der Meer PF. Flow cytometric assessment of agonist-induced P-selectin expression as a measure of platelet quality in stored platelet concentrates. Transfusion. 2013;53(8):1780-7.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Galan AM, Lozano M, Molina P, Navalon F, Marschner S, Goodrich R, et al. Impact of pathogen reduction technology and storage in platelet additive solutions on platelet function. Transfusion. 2011;51(4):808-15.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Johnson L, Winter KM, Reid S, Hartkopf-Theis T, Marschner S, Goodrich RP, et al. The effect of pathogen reduction technology (Mirasol) on platelet quality when treated in additive solution with low plasma carryover. Vox Sang. 2011; 101(3):208-14.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Reid S, Johnson L, Woodland N, Marks DC. Pathogen reduction treatment of buffy coat platelet concentrates in additive solution induces proapoptotic signaling. Transfusion. 2012;52(10):2094-103.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Castrillo A, Cardoso M, Rouse L. Treatment of buffy coat platelets in platelet additive solution with mirasol(®) pathogen reduction technology system. Transfus Med Hemother. 2013;40(1):44-8.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Ostrowski SR, Bochsen L, Salado-Jimena JA, Ullum H, Reynaerts I, Goodrich RP, et al. In vitro cell quality of buffy coat platelets in additive solution treated with pathogen reduction technology. Transfusion. 2010;50(10):2210-9.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Cookson P, Thomas S, Marschner S, Goodrich R, Cardigan R. In vitro quality of single-donor platelets treated with riboflavin and ultraviolet light and stored in platelet storage medium for up to 8 days. Transfusion. 2012;52(5):983-94.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Picker SM, Tauszig ME, Gathof BS. Cell quality of apheresis-derived platelets treated with riboflavin-ultraviolet light after resuspension in platelet additive solution. Transfusion. 2012;52(3):510-6.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Abonnenc M, Sonego G, Crettaz D, Aliotta A, Prudent M, Tissot JD, et al. In vitro study of platelet function confirms the contribution of the ultraviolet B (UVB) radiation in the lesions observed in riboflavin/UVB treated platelet concentrates. Transfusion. 2015;55(9):2219-30.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Zeddies S, De Cuyper IM, van der Meer PF, Daal BB, de Korte D, Gutiérrez L, et al. Pathogen reduction treatment using riboflavin and ultraviolet light impairs platelet reactivity toward specific agonists in vitro. Transfusion. 2014;54(9): 2292-300.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Osman A, Hitzler WE, Meyer CU, Landry P, Corduan A, Laffont B, et al. Effects of pathogen reduction systems on platelet microRNAs, mRNAs, activation, and function. Platelets. 2015;26(2):154-63.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Van Aelst B, Feys HB, Devloo R, Vanhoorelbeke K, Vandekerckhove P, Compernolle V. Riboflavin and amotosalen photochemicaltreatments of plateletconcentrates reduce thrombus formationkinetics in vitro. Vox Sang. 2015;108(4):328-39.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Ignatova AA, Karpova OV, Trakhtman PE, Rumiantsev SA, Panteleev MA. Functional characteristics and clinical effectiveness of platelet concentrates treated with riboflavin and ultraviolet light in plasma and in platelet additive solution. Vox Sang. 2016;110(3):244-52.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Perez-Pujol S, Tonda R, Lozano M, Fuste B, Lopez-Vilchez I, Galan AM, et al. Effects of a new pathogen-reductiontechnology (Mirasol PRT) on functional aspects of platelet concentrates. Transfusion. 2005;45(6):911-9.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Prudent M, D'Alessandro A, Cazenave JP, Devine DV, Gachet C, Greinacher A,et al. Proteome changes in platelets after pathogen inactivation - an interlaboratory consensus. Transfus Med Rev. 2014;28(2):72-83.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Rinder HM, Smith BR. In vitro evaluation of stored platelets: is there hope for predicting posttransfusion platelet survival and function? Transfusion. 2003;43(1):2-6.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Butler C, Doree C, Estcourt LJ, Trivella M, Hopewell S, Brunskill SJ, et al. Pathogen-reduced platelets for the prevention of bleeding. Cochrane Database Syst Rev. 2013;(3):CD009072.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Kerkhoffs JL, van Putten WL, Novotny VM, TeBoekhorst PA, Schipperus MR, Zwaginga JJ, et al. Clinical effectiveness of leucoreduced, pooled donor platelet concentrates, stored in plasma or additive solution with and without pathogen reduction. Br J Haematol. 2010;150(2):209-17.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Goodrich RP, Edrich RA, Li J, Seghatchian J. The Mirasol PRT system for pathogen reduction of platelets and plasma: an overview of current status and future trends. Transfus Apher Sci. 2006;35(1):5-17.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>AuBuchon JP, Herschel L, Roger J, Taylor H, Whitley P, Li J, et al. Efficacy of apheresis platelets treated with riboflavin and ultraviolet light for pathogen reduction. Transfusion. 2005;45(8):1335-41.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>A randomized controlled clinical trial evaluating the performance and safety of platelets treated with MIRASOL pathogen reduction technology. Transfusion. 2010;50(11):2362-75.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Stanojkovic Z, Balint B, Antic A, Todorovic M, Ostojic G, Pavlovic M. Clinical efficacy of riboflavin and ultraviolet light inactivated fresh frozen plasma evaluated with INR-quantification. Transfus Apher Sci. 2012;47(1):33-7.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Johansson PI, Simonsen AC, Brown PN, Ostrowski SR, Deberdt L, Van Hoydonck P, et al. A pilot study to assess the hemostatic function of pathogen-reduced platelets in patients with thrombocytopenia. Transfusion. 2013;53(9):2043-52.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Ypma PF, van der Meer PF, Heddle NM, van Hilten JA, Stijnen T, Middelburg RA, et al. A study protocol for a randomised controlled trial evaluating clinical effects of platelet transfusion products: the Pathogen Reduction Evaluation and Predictive Analytical Rating Score (PREPAReS) trial. BMJ Open. 2016;6(1):e010156.</mixed-citation></ref></ref-list></back></article>
