<?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">helmholtzeyeinstitute</journal-id><journal-title-group><journal-title xml:lang="ru">Российский офтальмологический журнал</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Ophthalmological Journal</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2072-0076</issn><issn pub-type="epub">2587-5760</issn><publisher><publisher-name>Real time Publishers</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21516/2072-0076-2023-16-4-152-158</article-id><article-id custom-type="elpub" pub-id-type="custom">helmholtzeyeinstitute-1370</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Иммунная привилегия в субретинальном пространстве и перспективы трансплантации ретинального пигментного эпителия при дегенеративных заболеваниях сетчатки</article-title><trans-title-group xml:lang="en"><trans-title>Immune privilege in the subretinal space and prospects of retinal pigment epithelium transplantation in degenerative diseases of the retina</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>Нероева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Neroeva</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Наталия Владимировна Нероева — канд. мед. наук, врач-офтальмолог отдела патологии сетчатки и зрительного нерва</p><p>ул. Садовая-Черногрязская, д. 14/19, Москва, 105062, Россия</p></bio><bio xml:lang="en"><p>Natalia V. Neroeva — Cand. of Med. Sci., ophthalmologist, department of retinal and optic nerve pathology</p><p>14/19, Sadovaya-Chernogryazskaya St., Moscow, 105062, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Балацкая</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Balatskaya</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Наталья Владимировна Балацкая — канд. биол. наук, начальник отдела иммунологии и вирусологии</p><p>ул. Садовая-Черногрязская, д. 14/19, Москва, 105062, Россия</p></bio><bio xml:lang="en"><p>Natalya V. Balatskaya — Cand. of Biol. Sci., head of the department of the immunology and virology</p><p>14/19, Sadovaya-Chernogryazskaya St., Moscow, 105062, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Катаргина</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Katargina</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Людмила Анатольевна Катаргина — д-р мед. наук, профессор, заместитель директора по науке</p><p>ул. Садовая-Черногрязская, д. 14/19, Москва, 105062, Россия</p></bio><bio xml:lang="en"><p>Ludmila A. Katargina — Dr. of Med. Sci., professor, deputy director</p><p>14/19, Sadovaya-Chernogryazskaya St., Moscow, 105062, Russia</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бриллиантова</surname><given-names>А. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Brilliantova</surname><given-names>A. G.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Ангелина Грантовна Бриллиантова — аспирант отдела патологии сетчатки и зрительного нерва</p><p>ул. Садовая-Черногрязская, д. 14/19, Москва, 105062, Россия</p></bio><bio xml:lang="en"><p>Angelina G. Brilliantova — PhD student, department of retinal and optic nerve pathology</p><p>14/19, Sadovaya-Chernogryazskaya St., Moscow, 105062, Russia</p></bio><email xlink:type="simple">angelinabrilliantova@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «НМИЦ глазных болезней им. Гельмгольца» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Helmholtz National Medical Research Center of Eye Diseases</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>29</day><month>12</month><year>2023</year></pub-date><volume>16</volume><issue>4</issue><fpage>152</fpage><lpage>158</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Нероева Н.В., Балацкая Н.В., Катаргина Л.А., Бриллиантова А.Г., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Нероева Н.В., Балацкая Н.В., Катаргина Л.А., Бриллиантова А.Г.</copyright-holder><copyright-holder xml:lang="en">Neroeva N.V., Balatskaya N.V., Katargina L.A., Brilliantova A.G.</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://roj.igb.ru/jour/article/view/1370">https://roj.igb.ru/jour/article/view/1370</self-uri><abstract><p>Поражение ретинального пигментного эпителия (РПЭ) лежит в основе патогенеза дегенеративно-дистрофических заболеваний сетчатки, в частности возрастной макулярной дегенерации (ВМД) — одной из ведущих причин необратимого снижения центрального зрения, слепоты и инвалидизации среди пожилого населения. Варианты терапии поздних стадий ВМД ограниченны и представлены ингибиторами ангиогенеза при влажной форме заболевания; эффективного лечения географической атрофии не существует, так как клетки РПЭ не способны к регенерации. Развитие биомедицинских наук, прогресс витреоретинальной хирургии инициировали поиск новых, высокотехнологичных способов лечения дегенеративных заболеваний сетчатки, направленных на восстановление РПЭ. Заместительная трансплантация индуцированными плюрипотентными стволовыми клетками (ИПСК), дифференцированными в РПЭ, представляется наиболее перспективным подходом для замены поврежденных элементов сетчатки и улучшения остроты зрения, а особенности глаза как иммунопривилегированного органа создают, по мнению ряда исследователей, относительно безопасные условия для субретинального введения ИПСК РПЭ. В обзоре систематизированы данные литературы, посвященной изучению иммунной привилегии в заднем отрезке глаза, а также результаты исследований в области субретинальной трансплантации СК; обсуждаются условия и возможные механизмы, запускающие отторжение трансплантата, методы, направленные на предотвращение реакции тканевой несовместимости.</p></abstract><trans-abstract xml:lang="en"><p>Damage of the retinal pigment epithelium (RPE) underlies the pathogenesis of degenerative-dystrophic diseases of the retina, in particular, age-related macular degeneration (AMD) — one of the leading causes of irreversible loss of central vision, blindness and elderly population disability. Advanced AMD treatment options are limited to angiogenesis inhibitors in the wet form of the disease; there is no effective treatment for geographic atrophy, since RPE cells are unable to regenerate. The advances of biomedicine and the progress of vitreoretinal surgery gave rise to searching new high-technology methods of degenerative retinal disease treatment, aimed at restoring RPE. Replacement transplantation with induced pluripotent stem cells (iPSCs) specifically oriented at RPE seems to be the most promising approach for replacing damaged retinal elements and improving visual acuity, while, as some researchers believe, the fact that the eye is an immune-privileged organ ensures relatively safe conditions for subretinal administration of iPSC-RPE. The review systematizes the literature data on immune privilege in the posterior eye segment, as well as the results of studies in the field of subretinal stem cells transplantation. The conditions and possible mechanisms that trigger graft rejection, methods aimed at preventing tissue incompatibility reactions are also discussed.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>дегенеративные заболевания сетчатки</kwd><kwd>ретинальный пигментный эпителий</kwd><kwd>иммунная привилегия субретинального пространства</kwd><kwd>трансплантация</kwd><kwd>иммуносупрессия</kwd></kwd-group><kwd-group xml:lang="en"><kwd>degenerative diseases of the retina</kwd><kwd>retinal pigment epithelium</kwd><kwd>ocular immune privilege of subretinal space</kwd><kwd>transplantation immunosuppression</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">Нolan V, Palacka K, Hermankova B. Mesenchymal stem cell-based therapy for retinal degenerative diseases: Experimental models and clinical trials. Cells. 2021; 10 (3): 588. https://doi.org/10.3390/cells10030588</mixed-citation><mixed-citation xml:lang="en">Нolan V, Palacka K, Hermankova B. Mesenchymal stem cell-based therapy for retinal degenerative diseases: Experimental models and clinical trials. Cells. 2021; 10 (3): 588. https://doi.org/10.3390/cells10030588</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Ugarte M, Hussain AA, Marshall J. An experimental study of the elastic properties of the human Bruch's membrane-choroid complex: relevance to ageing. Br J Ophthalmol. 2006; 90 (5): 621–6. doi: 10.1136/bjo.2005.086579</mixed-citation><mixed-citation xml:lang="en">Ugarte M, Hussain AA, Marshall J. An experimental study of the elastic properties of the human Bruch's membrane-choroid complex: relevance to ageing. Br J Ophthalmol. 2006; 90 (5): 621–6. doi: 10.1136/bjo.2005.086579</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Lim LS, Mitchell P, Seddon JM, Holz FG, Wong TY. Age-related macular degeneration. Lancet. 2012; 379 (9827): 1728–38. doi: 10.1016/S0140-6736(12)60282-7</mixed-citation><mixed-citation xml:lang="en">Lim LS, Mitchell P, Seddon JM, Holz FG, Wong TY. Age-related macular degeneration. Lancet. 2012; 379 (9827): 1728–38. doi: 10.1016/S0140-6736(12)60282-7</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Mitchell P, Liew G, Gopinath B, Wong T.Y. Age-related macular degeneration. Lancet. 2018; 392: 1147–59. doi: 10.1016/S0140-6736(18)31550-2</mixed-citation><mixed-citation xml:lang="en">Mitchell P, Liew G, Gopinath B, Wong T.Y. Age-related macular degeneration. Lancet. 2018; 392: 1147–59. doi: 10.1016/S0140-6736(18)31550-2</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Medawar P. Immunity to homologous grafted skin. III. The fate of skin homografts transplanted to the brain to subcutaneous tissue, and to the anterior chamber of the eye. Br J Exp Pathol. 1948; 29: 58–69.</mixed-citation><mixed-citation xml:lang="en">Medawar P. Immunity to homologous grafted skin. III. The fate of skin homografts transplanted to the brain to subcutaneous tissue, and to the anterior chamber of the eye. Br J Exp Pathol. 1948; 29: 58–69.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Cunha-Vaz J, Bernardes R, Lobo C. Blood-retinal barrier. Eur J Ophthalmol. 2011: 21 Suppl 6: S3-9. doi: 10.5301/EJO.2010.6049</mixed-citation><mixed-citation xml:lang="en">Cunha-Vaz J, Bernardes R, Lobo C. Blood-retinal barrier. Eur J Ophthalmol. 2011: 21 Suppl 6: S3-9. doi: 10.5301/EJO.2010.6049</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Dartt AD, Dana R, D'Amore P, Niederkorn J, eds. Immunology, inflammation and diseases of the eye. Academic Press. 2011: 50–57, 38–42.</mixed-citation><mixed-citation xml:lang="en">Dartt AD, Dana R, D'Amore P, Niederkorn J, eds. Immunology, inflammation and diseases of the eye. Academic Press. 2011: 50–57, 38–42.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor AW. Review of the activation of TGF-Beta in immunity. J Leukoc Biol. 2009; 85 (1): 29–33. doi:10.1189/jlb.0708415</mixed-citation><mixed-citation xml:lang="en">Taylor AW. Review of the activation of TGF-Beta in immunity. J Leukoc Biol. 2009; 85 (1): 29–33. doi:10.1189/jlb.0708415</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ferguson TA, Griffith TS. The role of Fas ligand and TNF-related apoptosisinducing ligand (TRAIL) in the ocular immune response. Chem Immunol Allergy. 2007; 92: 140–54. doi: 10.1159/000099265</mixed-citation><mixed-citation xml:lang="en">Ferguson TA, Griffith TS. The role of Fas ligand and TNF-related apoptosisinducing ligand (TRAIL) in the ocular immune response. Chem Immunol Allergy. 2007; 92: 140–54. doi: 10.1159/000099265</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Sugita S, Usui Y, Horie S, et al. T-cell suppression by programmed cell death 1 ligand 1 on retinal pigment epithelium during inflammatory conditions. Invest Ophthalmol Vis Sci. 2009; Jun; 50 (6): 2862–70. doi: 10.1167/iovs.08-2846</mixed-citation><mixed-citation xml:lang="en">Sugita S, Usui Y, Horie S, et al. T-cell suppression by programmed cell death 1 ligand 1 on retinal pigment epithelium during inflammatory conditions. Invest Ophthalmol Vis Sci. 2009; Jun; 50 (6): 2862–70. doi: 10.1167/iovs.08-2846</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Wenkel H, Streilein JW. Evidence that retinal pigment epithelium functions as an immune-privileged tissue. Invest Ophthalmol Vis Sci. 2000; 41 (11): 3467–73.</mixed-citation><mixed-citation xml:lang="en">Wenkel H, Streilein JW. Evidence that retinal pigment epithelium functions as an immune-privileged tissue. Invest Ophthalmol Vis Sci. 2000; 41 (11): 3467–73.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Jiang LQ, Jorquera M, Streilein JW. Subretinal space and vitreous cavity as immunologically privileged sites for retinal allografts. Invest OphthalmolVis Sci. November. 1993; 34: 3347–54.</mixed-citation><mixed-citation xml:lang="en">Jiang LQ, Jorquera M, Streilein JW. Subretinal space and vitreous cavity as immunologically privileged sites for retinal allografts. Invest OphthalmolVis Sci. November. 1993; 34: 3347–54.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Weisz JM, Humayun MS, De Juan EJ, et al. Allogenic fetal retinal pigment epithelial cell transplant in a patient with geographic atrophy. Retina. 1999; 19 (6): 540–5. doi:10.1097/00006982-199911000-00011</mixed-citation><mixed-citation xml:lang="en">Weisz JM, Humayun MS, De Juan EJ, et al. Allogenic fetal retinal pigment epithelial cell transplant in a patient with geographic atrophy. Retina. 1999; 19 (6): 540–5. doi:10.1097/00006982-199911000-00011</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Anderson DH, Radeke MJ, Gallo NB, et al. The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis revisited. Prog Retin Eye Res. 2010; 29: 95–112. doi: 10.1016/j.preteyeres.2009.11.003</mixed-citation><mixed-citation xml:lang="en">Anderson DH, Radeke MJ, Gallo NB, et al. The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis revisited. Prog Retin Eye Res. 2010; 29: 95–112. doi: 10.1016/j.preteyeres.2009.11.003</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Балацкая Н.В., Петров С.Ю., Котелин В.И. Факторы врожденного иммунитета в патогенезе глаукомы и оптической нейропатии. Иммунопатология, аллергология, инфектология. 2021; 1: 29–38.</mixed-citation><mixed-citation xml:lang="en">Balatskaya N.V., Petrov S.Yu., Kotelin V.I. Factors of innate immunity in the pathogenesis of glaucoma and optic neuropathy. Immunopatologija, allergologija, infektologija. 2021; 1: 29–38 (In Russ.). doi: 10.14427/jipai.2021.1.29</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Raoul W, Keller N, Rodero M, et al. Role of the chemokine receptor CX3CR1 in the mobilization of phagocytic retinal microglial cells. J Neuroimmunol. 2008; 198: 56–61. doi: 10.1016/j.jneuroim.2008.04.014</mixed-citation><mixed-citation xml:lang="en">Raoul W, Keller N, Rodero M, et al. Role of the chemokine receptor CX3CR1 in the mobilization of phagocytic retinal microglial cells. J Neuroimmunol. 2008; 198: 56–61. doi: 10.1016/j.jneuroim.2008.04.014</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Paglinawan R, Malipiero U, Schlapbach R, et al. TGF beta directs gene expression of activated microglia to an anti-inflammatory phenotype strongly focusing on chemokine genes and cell migratory genes. Glia. 2003; 44: 219–31. doi: 10.1002/glia.10286</mixed-citation><mixed-citation xml:lang="en">Paglinawan R, Malipiero U, Schlapbach R, et al. TGF beta directs gene expression of activated microglia to an anti-inflammatory phenotype strongly focusing on chemokine genes and cell migratory genes. Glia. 2003; 44: 219–31. doi: 10.1002/glia.10286</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mecha M, Carrillo-Salinas FJ, Feliu A, Mestre L, Guaza C. Microglia activation states and cannabinoid system: Therapeutic implications. Pharmacol Ther. 2016; 166: 40–55. doi: 10.1016/j.pharmthera.2016.06.011</mixed-citation><mixed-citation xml:lang="en">Mecha M, Carrillo-Salinas FJ, Feliu A, Mestre L, Guaza C. Microglia activation states and cannabinoid system: Therapeutic implications. Pharmacol Ther. 2016; 166: 40–55. doi: 10.1016/j.pharmthera.2016.06.011</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">De Simone R, Ambrosini E, Carnevale D, Ajmone-Cat MA, Minghetti L. NGF promotes microglial migration through the activation of its high affinity receptor: modulation by TGF-beta. J Neuroimmunol. 2007; 190: 53–60. doi:10.1016/j.jneuroim.2007.07.020</mixed-citation><mixed-citation xml:lang="en">De Simone R, Ambrosini E, Carnevale D, Ajmone-Cat MA, Minghetti L. NGF promotes microglial migration through the activation of its high affinity receptor: modulation by TGF-beta. J Neuroimmunol. 2007; 190: 53–60. doi:10.1016/j.jneuroim.2007.07.020</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Ng TF, Turpie B, Masli S. Thrombospondin-1-mediated regulation of microglia activation after retinal injury. Invest Ophthalmol Vis Sci. 2009; 50: 5472–8. doi:10.1167/iovs.08-2877</mixed-citation><mixed-citation xml:lang="en">Ng TF, Turpie B, Masli S. Thrombospondin-1-mediated regulation of microglia activation after retinal injury. Invest Ophthalmol Vis Sci. 2009; 50: 5472–8. doi:10.1167/iovs.08-2877</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Rashid K, Akhtar-Schaefer I, Langmann T. Microglia in retinal degeneration. Front Immunol. 2019; 10: 1975. doi: 10.3389/fimmu.2019.01975</mixed-citation><mixed-citation xml:lang="en">Rashid K, Akhtar-Schaefer I, Langmann T. Microglia in retinal degeneration. Front Immunol. 2019; 10: 1975. doi: 10.3389/fimmu.2019.01975</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor AW, Ng TF. Negative regulators that mediate ocular immune privilege. Journal of Leukocyte Biology. 2018 June; 103 (6): 1179–87. https://doi.org/10.1002/JLB.3MIR0817-337R</mixed-citation><mixed-citation xml:lang="en">Taylor AW, Ng TF. Negative regulators that mediate ocular immune privilege. Journal of Leukocyte Biology. 2018 June; 103 (6): 1179–87. https://doi.org/10.1002/JLB.3MIR0817-337R</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Zamiri P, Masli S, Kitaichi N, Taylor AW, Streilein JW. Thrombospondin plays a vital role in the immune privilege of the eye. Invest Ophthalmol Vis Sci. 2005; 46: 908–19. doi:10.1167/iovs.04-0362</mixed-citation><mixed-citation xml:lang="en">Zamiri P, Masli S, Kitaichi N, Taylor AW, Streilein JW. Thrombospondin plays a vital role in the immune privilege of the eye. Invest Ophthalmol Vis Sci. 2005; 46: 908–19. doi:10.1167/iovs.04-0362</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Nishida T, Miyata S, Itoh Y, et al. Anti-inflammatory effects of alphamelanocytestimulating hormone against rat endotoxin-induced uveitis and the time course of inflammatory agents in aqueous humor. Int Immunopharmacol. 2004; 4: 1059–66. doi: 10.1016/j.intimp.2004.04.011</mixed-citation><mixed-citation xml:lang="en">Nishida T, Miyata S, Itoh Y, et al. Anti-inflammatory effects of alphamelanocytestimulating hormone against rat endotoxin-induced uveitis and the time course of inflammatory agents in aqueous humor. Int Immunopharmacol. 2004; 4: 1059–66. doi: 10.1016/j.intimp.2004.04.011</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Kawazoe Y, Sugita S, Keino H, et al. Retinoic acid from retinal pigment epithelium induces T regulatory cells. Exp Eye Res. 2012; 94: 32–40. doi: 10.1016/j.exer.2011.11.002</mixed-citation><mixed-citation xml:lang="en">Kawazoe Y, Sugita S, Keino H, et al. Retinoic acid from retinal pigment epithelium induces T regulatory cells. Exp Eye Res. 2012; 94: 32–40. doi: 10.1016/j.exer.2011.11.002</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Sugita S, Horie S, Nakamura O, et al. Retinal pigment epithelium derived CTLA-2 alpha induces TGF beta-producing T regulatory cells. Immunol. 2008; 181: 7525–36. doi: 10.4049/jimmunol.181.11.7525</mixed-citation><mixed-citation xml:lang="en">Sugita S, Horie S, Nakamura O, et al. Retinal pigment epithelium derived CTLA-2 alpha induces TGF beta-producing T regulatory cells. Immunol. 2008; 181: 7525–36. doi: 10.4049/jimmunol.181.11.7525</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Hirsch L, Nazari H, Sreekumar PG, et al. TGF- 2 secretion from RPE decreases with polarization and becomes apically oriented. Cytokine. 2015; 71 (2): 394–6. doi: 10.1016/j.cyto.2014.11.014</mixed-citation><mixed-citation xml:lang="en">Hirsch L, Nazari H, Sreekumar PG, et al. TGF- 2 secretion from RPE decreases with polarization and becomes apically oriented. Cytokine. 2015; 71 (2): 394–6. doi: 10.1016/j.cyto.2014.11.014</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Getting SJ, Lam CW, Chen AS, Grieco P, Perretti M. Melanocortin 3 receptors control crystal-induced inflammation. FASEB J. 2006; 20: 2234–41. doi: 10.1096/fj.06-6339com</mixed-citation><mixed-citation xml:lang="en">Getting SJ, Lam CW, Chen AS, Grieco P, Perretti M. Melanocortin 3 receptors control crystal-induced inflammation. FASEB J. 2006; 20: 2234–41. doi: 10.1096/fj.06-6339com</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor AW, Streilein JW, Cousins SW. Identification of alphamelanocyte stimulating hormone as a potential immunosuppressive factor in aqueous-humor. Curr Eye Res. 1992; 11: 1199–206. 21. doi: 10.3109/02713689208999545</mixed-citation><mixed-citation xml:lang="en">Taylor AW, Streilein JW, Cousins SW. Identification of alphamelanocyte stimulating hormone as a potential immunosuppressive factor in aqueous-humor. Curr Eye Res. 1992; 11: 1199–206. 21. doi: 10.3109/02713689208999545</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Taylor AW, Lee DJ. The alpha-melanocyte stimulating hormone induces conversion of effector Tcells into treg cells. J Transplant. 2011; 246856. doi: 10.1155/2011/246856</mixed-citation><mixed-citation xml:lang="en">Taylor AW, Lee DJ. The alpha-melanocyte stimulating hormone induces conversion of effector Tcells into treg cells. J Transplant. 2011; 246856. doi: 10.1155/2011/246856</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Keino H, Horie S, Sugita S. Immune privilege and eye-derived T-regulatory cells. J Immunol Res. 2018; 1679197. doi: 10.1155/2018/1679197</mixed-citation><mixed-citation xml:lang="en">Keino H, Horie S, Sugita S. Immune privilege and eye-derived T-regulatory cells. J Immunol Res. 2018; 1679197. doi: 10.1155/2018/1679197</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Wilbanks GA, Streilein JW. Studies on the Induction of Anterior Chamber- Associated Immune Deviation (ACAID). 1. Evidence that an antigen-specific, ACAID-inducing, Cell-Associated Signal exists in the peripheral blood. J Immunol. 1991; 146 (8): 2610–7.</mixed-citation><mixed-citation xml:lang="en">Wilbanks GA, Streilein JW. Studies on the Induction of Anterior Chamber- Associated Immune Deviation (ACAID). 1. Evidence that an antigen-specific, ACAID-inducing, Cell-Associated Signal exists in the peripheral blood. J Immunol. 1991; 146 (8): 2610–7.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Faunce DE, Stein-Streilein J. NKT Cell-Derived RANTES recruits APCs and CD8+ T Cells to the spleen during the generation of regulatory T cells in tolerance. J Immunol. 2002; 169 (1): 31–8. doi: 10.4049/jimmunol.169.1.31</mixed-citation><mixed-citation xml:lang="en">Faunce DE, Stein-Streilein J. NKT Cell-Derived RANTES recruits APCs and CD8+ T Cells to the spleen during the generation of regulatory T cells in tolerance. J Immunol. 2002; 169 (1): 31–8. doi: 10.4049/jimmunol.169.1.31</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Нероев В.В., Балацкая Н.В., Ченцова Е.В., Шамхалова Х.М. Механизмы иммунорегуляции и трансплантационный иммунитет при пересадках роговицы. Медицинская иммунология. 2020; 22 (1): 61–76.</mixed-citation><mixed-citation xml:lang="en">Neroev V.V., Balatskaya N.V., Chentsova E.V., Shamkhalova Kh.M. Mechanisms of immunoregulation and transplantation immunity during corneal transplantation. Мedicinskaja immunologija. 2020; 22 (1): 61–76 (In Russ.). https://doi.org/10.15789/1563-0625-MOI-1768</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou R, Caspi RR. Ocular immune privilege. F1000 Biol Rep. 2010 Jan 18; 2: 3. doi:10.3410/B2-3</mixed-citation><mixed-citation xml:lang="en">Zhou R, Caspi RR. Ocular immune privilege. F1000 Biol Rep. 2010 Jan 18; 2: 3. doi:10.3410/B2-3</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Petrash CC, Palestine AG, Canto-Soler MV. Immunologic rejection of transplanted retinal Pigmented epithelium: mechanisms and strategies for prevention. Front Immunol. 2021; 12: 621007. doi: 10.3389/fimmu.2021.621007</mixed-citation><mixed-citation xml:lang="en">Petrash CC, Palestine AG, Canto-Soler MV. Immunologic rejection of transplanted retinal Pigmented epithelium: mechanisms and strategies for prevention. Front Immunol. 2021; 12: 621007. doi: 10.3389/fimmu.2021.621007</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Canto-Soler V, Flores-Bellver M, Vergara MN. Stem cell sources and their potential for the treatment of retinal degenerations. Invest Ophthalmol Vis Sci. 57. 2016; 2016 Apr 1; 57 (5): ORSFd1-9. doi: 10.1167/iovs.16-19127</mixed-citation><mixed-citation xml:lang="en">Canto-Soler V, Flores-Bellver M, Vergara MN. Stem cell sources and their potential for the treatment of retinal degenerations. Invest Ophthalmol Vis Sci. 57. 2016; 2016 Apr 1; 57 (5): ORSFd1-9. doi: 10.1167/iovs.16-19127</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Marei HE, Althani A, Lashen S, Cenciarelli C, Hasan A. Genetically unmatched human iPSC and ESC exhibit equivalent gene expression and neuronal differentiation potential. Sci Rep. 2017; 7 (1): 17504. doi: 10.1038/s41598-017-17882-1</mixed-citation><mixed-citation xml:lang="en">Marei HE, Althani A, Lashen S, Cenciarelli C, Hasan A. Genetically unmatched human iPSC and ESC exhibit equivalent gene expression and neuronal differentiation potential. Sci Rep. 2017; 7 (1): 17504. doi: 10.1038/s41598-017-17882-1</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Li Y, Tsai YT, Hsu CW, et al. Long-term safety and efficacy of human-induced pluripotent stem cell (iPS) grafts in a preclinical model of retinitis pigmentosa. Molec Med. 2012; 18 (1): 1312–9. doi: 10.2119/molmed.2012.00242</mixed-citation><mixed-citation xml:lang="en">Li Y, Tsai YT, Hsu CW, et al. Long-term safety and efficacy of human-induced pluripotent stem cell (iPS) grafts in a preclinical model of retinitis pigmentosa. Molec Med. 2012; 18 (1): 1312–9. doi: 10.2119/molmed.2012.00242</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Sugita S, Makabe K, Fujii S, et al. Detection of retinal pigment epithelium-specific antibody in Ipsc-derived retinal pigment epithelium transplantation models. Stem Cell Rep. 2017; 9 (5): 1501–15. doi: 10.1016/j.stemcr.2017.10.003</mixed-citation><mixed-citation xml:lang="en">Sugita S, Makabe K, Fujii S, et al. Detection of retinal pigment epithelium-specific antibody in Ipsc-derived retinal pigment epithelium transplantation models. Stem Cell Rep. 2017; 9 (5): 1501–15. doi: 10.1016/j.stemcr.2017.10.003</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Davis RJ, Alam NM, Zhao C, et al. The developmental stage of adult human stem cell-derived retinal pigment epithelium cells influences transplant efficacy for vision rescue. Stem Cell Reports. 2017; 9: 42–9. doi: 10.1016/j.stemcr.2017.05.016</mixed-citation><mixed-citation xml:lang="en">Davis RJ, Alam NM, Zhao C, et al. The developmental stage of adult human stem cell-derived retinal pigment epithelium cells influences transplant efficacy for vision rescue. Stem Cell Reports. 2017; 9: 42–9. doi: 10.1016/j.stemcr.2017.05.016</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Stanzel B, Ader M, Liu Z, et al. Surgical approaches for cell therapeutics delivery to the retinal pigment epithelium and retina. Adv Exp Med Biol. 2019; 1186: 141–70. doi:10.1007/978-3-030-28471-8_6</mixed-citation><mixed-citation xml:lang="en">Stanzel B, Ader M, Liu Z, et al. Surgical approaches for cell therapeutics delivery to the retinal pigment epithelium and retina. Adv Exp Med Biol. 2019; 1186: 141–70. doi:10.1007/978-3-030-28471-8_6</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Z, Parikh BH, Tan QSW, et al. Surgical transplantation of human RPE stem cell-derived RPE monolayers into non-human primates with immunosuppression. Stem cell Reports. 2021; 16 (2): 237–51. doi: 10.1016/j.stemcr.2020.12.007</mixed-citation><mixed-citation xml:lang="en">Liu Z, Parikh BH, Tan QSW, et al. Surgical transplantation of human RPE stem cell-derived RPE monolayers into non-human primates with immunosuppression. Stem cell Reports. 2021; 16 (2): 237–51. doi: 10.1016/j.stemcr.2020.12.007</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">McGill TJ, Stoddard J, Renner LM, et al. Allogeneic Ipsc-Derived RPE cell graft failure following transplantation into the subretinal space in nonhuman primates. Invest Ophthalmol Vis Sci. 2018; 59: 1374–83. doi:10.1167/iovs.17-22467</mixed-citation><mixed-citation xml:lang="en">McGill TJ, Stoddard J, Renner LM, et al. Allogeneic Ipsc-Derived RPE cell graft failure following transplantation into the subretinal space in nonhuman primates. Invest Ophthalmol Vis Sci. 2018; 59: 1374–83. doi:10.1167/iovs.17-22467</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Rezai KA, Farrokh-Siar L, Godowski K, Patel SC, Ernest JT. A model for xenogenic immune response. Graefes Arch Clin Exp Ophthalmol. 2000; 238: 352–8. doi: 10.1007/s004170050364</mixed-citation><mixed-citation xml:lang="en">Rezai KA, Farrokh-Siar L, Godowski K, Patel SC, Ernest JT. A model for xenogenic immune response. Graefes Arch Clin Exp Ophthalmol. 2000; 238: 352–8. doi: 10.1007/s004170050364</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Ilmarinen T, Hiidenmaa H, K bi P, et al. Ultrathin polyimide membrane as cell carrier for subretinal transplantation of human embryonic stem cell derived retinal pigment epithelium. PLoS One. 2015; 10 (11): e0143669. doi: 10.1371/journal.pone.0143669</mixed-citation><mixed-citation xml:lang="en">Ilmarinen T, Hiidenmaa H, K bi P, et al. Ultrathin polyimide membrane as cell carrier for subretinal transplantation of human embryonic stem cell derived retinal pigment epithelium. PLoS One. 2015; 10 (11): e0143669. doi: 10.1371/journal.pone.0143669</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Gosset C, Lefaucheur C, Glotz D. New insights in antibody-mediated rejection. Curr Opin Nephrol Hypertens. 2014; 23: 597–604. doi:10.1097/MNH.0000000000000069</mixed-citation><mixed-citation xml:lang="en">Gosset C, Lefaucheur C, Glotz D. New insights in antibody-mediated rejection. Curr Opin Nephrol Hypertens. 2014; 23: 597–604. doi:10.1097/MNH.0000000000000069</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Kennelly KP, Holmes TM, Wallace DM, O’Farrelly C, Keegan DJ. Early subretinal allograft rejection is characterized by innate immune activity. Cell Transplant. 2017; 26: 983–1000. doi: 10.3727/096368917X694697</mixed-citation><mixed-citation xml:lang="en">Kennelly KP, Holmes TM, Wallace DM, O’Farrelly C, Keegan DJ. Early subretinal allograft rejection is characterized by innate immune activity. Cell Transplant. 2017; 26: 983–1000. doi: 10.3727/096368917X694697</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Takeuchi O, Akira S. Pattern recognition receptors and inflammation. Cell. 2010; 140: 805–20. doi: 10.1016/j.cell.2010.01.022</mixed-citation><mixed-citation xml:lang="en">Takeuchi O, Akira S. Pattern recognition receptors and inflammation. Cell. 2010; 140: 805–20. doi: 10.1016/j.cell.2010.01.022</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Tinckam KJ, Djurdjev O, Magil AB. Glomerular monocytes predict worse outcomes after acute renal allograft rejection independent of C4d status. Kidney Int. 2005; 68: 1866–74. doi: 10.1111/j.1523-1755.2005.00606</mixed-citation><mixed-citation xml:lang="en">Tinckam KJ, Djurdjev O, Magil AB. Glomerular monocytes predict worse outcomes after acute renal allograft rejection independent of C4d status. Kidney Int. 2005; 68: 1866–74. doi: 10.1111/j.1523-1755.2005.00606</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Ma FY, Woodman N, Mulley WR, Kanellis J, Nikolic-Paterson DJ. Macrophages сontribute to сellular but not humoral mechanisms of acute rejection in rat renal allografts. Transplantation. 2013; 96: 949–57. doi:10.1097/TP.0b013e3182a4befa</mixed-citation><mixed-citation xml:lang="en">Ma FY, Woodman N, Mulley WR, Kanellis J, Nikolic-Paterson DJ. Macrophages сontribute to сellular but not humoral mechanisms of acute rejection in rat renal allografts. Transplantation. 2013; 96: 949–57. doi:10.1097/TP.0b013e3182a4befa</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Kramer J, Chirco KR, Lamba DA. Immunological сonsiderations for retinal stem cell therapy. Adv Exp Med Biol. 2019; 1186: 99–119. doi:10.1007/978-3-030-28471-8_4</mixed-citation><mixed-citation xml:lang="en">Kramer J, Chirco KR, Lamba DA. Immunological сonsiderations for retinal stem cell therapy. Adv Exp Med Biol. 2019; 1186: 99–119. doi:10.1007/978-3-030-28471-8_4</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Yu C, Roubeix C, Sennlaub F, Saban DR. Microglia versus monocytes: distinct roles in degenerative diseases of the retina. Trends Neurosci. 2020; 43: 433–49. doi: 10.1016/j.tins.2020.03.012</mixed-citation><mixed-citation xml:lang="en">Yu C, Roubeix C, Sennlaub F, Saban DR. Microglia versus monocytes: distinct roles in degenerative diseases of the retina. Trends Neurosci. 2020; 43: 433–49. doi: 10.1016/j.tins.2020.03.012</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Martinez FO, Helming L, Gordon S. Alternative activation of macrophages: an immunologic functional perspective. Annu Rev Immunol. 2009; 27: 451–83. doi: 10.1146/annurev.immunol.021908.132532</mixed-citation><mixed-citation xml:lang="en">Martinez FO, Helming L, Gordon S. Alternative activation of macrophages: an immunologic functional perspective. Annu Rev Immunol. 2009; 27: 451–83. doi: 10.1146/annurev.immunol.021908.132532</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Noell WK, Walker VS, Kang BS, Berman S. Retinal damage by light in rats. Invest Ophthalmol. 1966; 5: 450–73.</mixed-citation><mixed-citation xml:lang="en">Noell WK, Walker VS, Kang BS, Berman S. Retinal damage by light in rats. Invest Ophthalmol. 1966; 5: 450–73.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Karlstetter M, Scholz R, Rutar M, et al. Retinal microglia: just bystander or target for therapy? Prog Retin Eye Res. 2015; 45: 30–57. doi: c10.1016/j.preteyeres.2014.11.004</mixed-citation><mixed-citation xml:lang="en">Karlstetter M, Scholz R, Rutar M, et al. Retinal microglia: just bystander or target for therapy? Prog Retin Eye Res. 2015; 45: 30–57. doi: c10.1016/j.preteyeres.2014.11.004</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Cuenca N, Fernandez-Sanchez L, Campello L, et al. Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases. Prog Retin Eye Res. 2014; 43: 17–75. doi: 10.1016/j.preteyeres.2014.07.001</mixed-citation><mixed-citation xml:lang="en">Cuenca N, Fernandez-Sanchez L, Campello L, et al. Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases. Prog Retin Eye Res. 2014; 43: 17–75. doi: 10.1016/j.preteyeres.2014.07.001</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Gordon S, Martinez FO. Alternative activation of macrophages: mechanism and functions. Immunity. 2010; 32: 593–604. doi: 10.1016/j.immuni.2010.05.007</mixed-citation><mixed-citation xml:lang="en">Gordon S, Martinez FO. Alternative activation of macrophages: mechanism and functions. Immunity. 2010; 32: 593–604. doi: 10.1016/j.immuni.2010.05.007</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Martinez FO, Gordon S. The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000 Prime Rep. 2014; 6: 13. doi: c10.12703/P6-13</mixed-citation><mixed-citation xml:lang="en">Martinez FO, Gordon S. The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000 Prime Rep. 2014; 6: 13. doi: c10.12703/P6-13</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Yin Y, Henzl MT, Lorber B, et al. Oncomodulin is a macrophage-derived signal for axon regeneration in retinal ganglion cells. Nat Neurosci. 2006; 9: 843–52. doi: 10.1038/nn1701</mixed-citation><mixed-citation xml:lang="en">Yin Y, Henzl MT, Lorber B, et al. Oncomodulin is a macrophage-derived signal for axon regeneration in retinal ganglion cells. Nat Neurosci. 2006; 9: 843–52. doi: 10.1038/nn1701</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Suh HS, Zhao ML, Derico L, Choi N, Lee SC. Insulin-like growth factor 1 and 2 (IGF1, IGF2) expression in human microglia: differential regulation by inflammatory mediators. J Neuroinflamm. 2013; 10: 37. doi: 10.1186/1742-2094-10-37</mixed-citation><mixed-citation xml:lang="en">Suh HS, Zhao ML, Derico L, Choi N, Lee SC. Insulin-like growth factor 1 and 2 (IGF1, IGF2) expression in human microglia: differential regulation by inflammatory mediators. J Neuroinflamm. 2013; 10: 37. doi: 10.1186/1742-2094-10-37</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Sugita S, Mandai M, Kamao H, Takahashi M. Immunological aspects of RPE cell transplantation. Prog Retin Eye Res. 2021; 84: 100950. doi: 10.1016/j.preteyeres.2021.100950</mixed-citation><mixed-citation xml:lang="en">Sugita S, Mandai M, Kamao H, Takahashi M. Immunological aspects of RPE cell transplantation. Prog Retin Eye Res. 2021; 84: 100950. doi: 10.1016/j.preteyeres.2021.100950</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Нероев В.В., Балацкая Н.В., Светлова Е.В. и др. Особенности локальной экспрессии мРНК, IL-1 , IL-18, CCL2/MCP-1 при моделировании атрофии пигментного эпителия и дегенерации сетчатки в эксперименте на кроликах. Молекулярная медицина. 2021; 2: 54–9.</mixed-citation><mixed-citation xml:lang="en">Neroev V.V., Balatskaya N.V., Svetlova E.V., et al. Features of local expression of mRNA, IL-1 , IL-18, CCL2/MCP-1 in the modeling of pigment epithelium atrophy and retinal degeneration in an experiment on rabbits. Molecular medicine. 2021; 2: 54–9 (In Russ.). doi: https://doi.org/10.29296/24999490-2021-02-08</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Нероев В.В., Балацкая Н.В., Светлова Е.В. и др. Изучение локальной экспрессии мРНК генов медиаторов воспаления в модели атрофии ретинального пигментного эпителия и дегенерации сетчатки, индуцированной субретинальным введением физиологического раствора в эксперименте у кроликов. Медицинская иммунология. 2021; 23 (4): 813–8.</mixed-citation><mixed-citation xml:lang="en">Neroev V.V., Balatskaya N.V., Svetlova E.V., et al. Examining locally expressed mrna of inflammatory mediator genes in a model of retinal pigment epithelium atrophy and retinal degeneration induced by subretinal saline injection in rabbits. Medical immunology (Russia). 2021; 23 (4): 813–8 (In Russ.). https://doi.org/10.15789/1563-0625-ELE-2255</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Нероева Н.В., Балацкая Н.В., Нероев В.В. и др. Особенности локальной экспрессии генов цитокинов иммунного ответа, трофических и вазорегулирующих факторов при моделировании атрофии ретинального пигментного эпителия. Бюллетень экспериментальной биологии и медицины. 2021; 172 (10): 466–73.</mixed-citation><mixed-citation xml:lang="en">Neroeva N.V., Balatskaya N.V., Neroev V.V., et al. Features of local expression of genes of immune response cytokines, trophic and vasoregulatory factors in the modeling of atrophy of the retinal pigment epithelium. Bulletin of experimental biology and medicine. 2021; 172 (10): 466–73 (In Russ.). https://doi.org/10.29296/24999490-2021-02-08</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Fujii S, Sugita S, Futatsugi Y, et al. Strategy for personalized treatment of iPSRetinal immune rejections assessed in cynomolgus monkey models. Int J Mol Sci. 2020; 21 (9): 3077. doi: 10.3390/ijms21093077</mixed-citation><mixed-citation xml:lang="en">Fujii S, Sugita S, Futatsugi Y, et al. Strategy for personalized treatment of iPSRetinal immune rejections assessed in cynomolgus monkey models. Int J Mol Sci. 2020; 21 (9): 3077. doi: 10.3390/ijms21093077</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Bali S, Filek R, Si F, Hodge W. Systemic immunosuppression in high-risk penetrating keratoplasty: A Systematic Review. J ClinMed Res. 2016; 8 (4): 269–76. doi: 10.14740/jocmr2326w</mixed-citation><mixed-citation xml:lang="en">Bali S, Filek R, Si F, Hodge W. Systemic immunosuppression in high-risk penetrating keratoplasty: A Systematic Review. J ClinMed Res. 2016; 8 (4): 269–76. doi: 10.14740/jocmr2326w</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Xian B, Huang B. The immune response of stem cells in subretinal transplantation. Stem Cell Res Ther. 2015; 6: 161. https://doi.org/10.1186/s13287-015-0167-1</mixed-citation><mixed-citation xml:lang="en">Xian B, Huang B. The immune response of stem cells in subretinal transplantation. Stem Cell Res Ther. 2015; 6: 161. https://doi.org/10.1186/s13287-015-0167-1</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Crafoord S, Algvere PV, Kopp ED, Seregard S. Cyclosporine treatment of RPE allografts in the rabbit subretinal space. Acta Ophthalmol Scand. 2000; 78 (2): 122–9. doi: 10.1034/j.1600-0420.2000.078002122.x</mixed-citation><mixed-citation xml:lang="en">Crafoord S, Algvere PV, Kopp ED, Seregard S. Cyclosporine treatment of RPE allografts in the rabbit subretinal space. Acta Ophthalmol Scand. 2000; 78 (2): 122–9. doi: 10.1034/j.1600-0420.2000.078002122.x</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Schwartz SD, Regillo CD, Lam BL, et al. Human embryonic stem cellderived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies. Lancet. 2015; 385 (9967): 509–16. doi: 10.1016/S0140-6736(14)61376-3</mixed-citation><mixed-citation xml:lang="en">Schwartz SD, Regillo CD, Lam BL, et al. Human embryonic stem cellderived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies. Lancet. 2015; 385 (9967): 509–16. doi: 10.1016/S0140-6736(14)61376-3</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>
