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<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">ssmu</journal-id><journal-title-group><journal-title xml:lang="ru">Бюллетень сибирской медицины</journal-title><trans-title-group xml:lang="en"><trans-title>Bulletin of Siberian Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1682-0363</issn><issn pub-type="epub">1819-3684</issn><publisher><publisher-name>Siberian State Medical University, the Ministry of Healthcare of the Russian Federation</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.20538/1682-0363-2006-3-98-104</article-id><article-id custom-type="elpub" pub-id-type="custom">ssmu-3098</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>ОТ НАУКИ К ПРАКТИКЕ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>FROM SCIENCE TO PRACTICE</subject></subj-group></article-categories><title-group><article-title>Полиморфизм гена хемокинового рецептора CCR5 у больных рассеянным склерозом в Сибирском регионе</article-title><trans-title-group xml:lang="en"><trans-title>Polymorphism of chemokine receptor gene CCR5 in multiple sclerosis patients and in healthy subjects in the Siberian region</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>Орлова</surname><given-names>Ю. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Orlova</surname><given-names>Yu. Yu.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Алифирова</surname><given-names>В. М.</given-names></name><name name-style="western" xml:lang="en"><surname>Alifirova</surname><given-names>V. M.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Чердынцева</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Cherdyntseva</surname><given-names>N. V.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гервас</surname><given-names>П. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Gervas</surname><given-names>P. A.</given-names></name></name-alternatives><email xlink:type="simple">noemail@neicon.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>Сибирский государственный медицинский университет</institution><country>Russian Federation</country></aff><aff xml:lang="ru" id="aff-2"><institution>НИИ онкологии ТНЦ СО РАМН</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2006</year></pub-date><pub-date pub-type="epub"><day>30</day><month>09</month><year>2006</year></pub-date><volume>5</volume><issue>3</issue><fpage>98</fpage><lpage>104</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Орлова Ю.Ю., Алифирова В.М., Чердынцева Н.В., Гервас П.А., 2006</copyright-statement><copyright-year>2006</copyright-year><copyright-holder xml:lang="ru">Орлова Ю.Ю., Алифирова В.М., Чердынцева Н.В., Гервас П.А.</copyright-holder><copyright-holder xml:lang="en">Orlova Y.Y., Alifirova V.M., Cherdyntseva N.V., Gervas P.A.</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://bulletin.ssmu.ru/jour/article/view/3098">https://bulletin.ssmu.ru/jour/article/view/3098</self-uri><abstract><p>Рассеянный склероз (РС) — хроническое воспалительное заболевание центральной нервный системы, в развитии которого ведущее значение имеют Тх1 типа. Хемокины и их рецепторы участвуют в развитии РС вследствие привлечения иммунных клеток в центральную нервную систему. Мутация CCR5 delta32 уменьшает функциональную активность соответствующего рецептора на клеточной поверхности и тем самым может редуцировать миграцию лейкоцитов в очаги поражения. С целью изучения роли мутации при РС сравнилась частота генотипа CCR5 в периферических мононуклеарах 102 больных РС и 136 здоровых лиц. Полученные результаты позволяют заключить, что полиморфизм гена хемокинового рецептора CCR5del32 не является ведущим фактором в восприимчивости к рассеянному склерозу в изученной популяции.</p></abstract><trans-abstract xml:lang="en"><p>Multiple sclerosis is chronic inflammatory disease of the central nervous system in the development of which chemokines of the type Tx1 play the leading role. Chemokines and their receptors participate in the development of multiple sclerosis as a result of drawing immune cells into central nervous system. Mutation of CCR5 delta32 decreases functional activity of the appropriate receptor on cellular surface and thus can reduce migration of leucocytes into foci of injury. Aimed at studying the role of mutation in multiple sclerosis, we compared frequency of gene type CCR5 in peripheral mononuclears of 102 multiple sclerosis patients and in 136 healthy subjects. The results obtained allow to conclude that polymorphism of chemokine receptor gene CCR5del32 is not a leading factor in the susceptibility to multiple sclerosis in the studied population.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>рассеянный склероз</kwd><kwd>хемокиновый рецептор</kwd><kwd>полиморфизм</kwd><kwd>multiple sclerosis</kwd><kwd>chemokine receptor</kwd><kwd>polymorphism</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">Галеева А.Р., Хаснутдинова Э.К., Сломинский П.А., Лимборская С.А. Распространенность делеции 32 п.н. в гене рецептора хемокинов CCR5 в популяциях Волго-Уральского региона // Генетика. 1998. Т. 34. № 8. С. 1160—1162.</mixed-citation><mixed-citation xml:lang="en">Галеева А.Р., Хаснутдинова Э.К., Сломинский П.А., Лимборская С.А. Распространенность делеции 32 п.н. в гене рецептора хемокинов CCR5 в популяциях Волго-Уральского региона // Генетика. 1998. Т. 34. № 8. С. 1160—1162.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Гусев Е.И., Бойко А.Н. Рассеянный склероз: от изучения иммунопатогенеза к новым методам лечения. М., 2001. 128 с.</mixed-citation><mixed-citation xml:lang="en">Гусев Е.И., Бойко А.Н. Рассеянный склероз: от изучения иммунопатогенеза к новым методам лечения. М., 2001. 128 с.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Завалишин И.А., Захарова М.Н. Рассеянный склероз: основные аспекты патогенеза // Рассеянный склероз и другие демиелинизирующие заболевания / Под ред. Е.И. Гусева, И.А. Завалишина, А.Н. Бойко. М.: Миклош, 2004. С. 60—74.</mixed-citation><mixed-citation xml:lang="en">Завалишин И.А., Захарова М.Н. Рассеянный склероз: основные аспекты патогенеза // Рассеянный склероз и другие демиелинизирующие заболевания / Под ред. Е.И. Гусева, И.А. Завалишина, А.Н. Бойко. М.: Миклош, 2004. С. 60—74.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Иерусалимский А.П., Малкова Н.А. Эпидемиологические исследования и их роль в изучении рассеяного склероза // Рассеянный склероз. Избранные вопросы теории и практики / Под ред. И.А. Завалишина, В.И. Головкина. М., 2000. С. 510—536.</mixed-citation><mixed-citation xml:lang="en">Иерусалимский А.П., Малкова Н.А. Эпидемиологические исследования и их роль в изучении рассеяного склероза // Рассеянный склероз. Избранные вопросы теории и практики / Под ред. И.А. Завалишина, В.И. Головкина. М., 2000. С. 510—536.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Посвалюк Н.Э., Козлова Т.А., Цеферман А.Г. Клинико-эпидемиологическая характеристика рассеянного склероза в Хабаровском крае // Рассеянный склероз (эпидемиология, новые методы диагностики). Новосибирск, 1985. С. 10—12.</mixed-citation><mixed-citation xml:lang="en">Посвалюк Н.Э., Козлова Т.А., Цеферман А.Г. Клинико-эпидемиологическая характеристика рассеянного склероза в Хабаровском крае // Рассеянный склероз (эпидемиология, новые методы диагностики). Новосибирск, 1985. С. 10—12.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Сломинский П.А., Шадрина М.И., Спицын В.А. и др. Простой и быстрый метод определения делеции 32 п.н. в гене рецептора хемокинов CCR5 // Генетика. 1997. Т. 33. № 11. С. 1596—1598.</mixed-citation><mixed-citation xml:lang="en">Сломинский П.А., Шадрина М.И., Спицын В.А. и др. Простой и быстрый метод определения делеции 32 п.н. в гене рецептора хемокинов CCR5 // Генетика. 1997. Т. 33. № 11. С. 1596—1598.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Ходос Х.Г., Кожова И.И. Рассеяный склероз. Иркутск: Восточ.-Сиб. кн. изд-во, 1980. 176 с.</mixed-citation><mixed-citation xml:lang="en">Ходос Х.Г., Кожова И.И. Рассеяный склероз. Иркутск: Восточ.-Сиб. кн. изд-во, 1980. 176 с.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Ebers G.C., Kukay K., Bulman D.E. et al. A full genome search in multiple sclerosis // Nat. Genet 1996. № 13. P. 472—476.</mixed-citation><mixed-citation xml:lang="en">Ebers G.C., Kukay K., Bulman D.E. et al. A full genome search in multiple sclerosis // Nat. Genet 1996. № 13. P. 472—476.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Sawcer S., Jones H.B., Feakes R. et al. A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 // Nat. Genet. 1996. № 13. P.464—468.</mixed-citation><mixed-citation xml:lang="en">Sawcer S., Jones H.B., Feakes R. et al. A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 // Nat. Genet. 1996. № 13. P.464—468.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Garred P., Madsen H., Petersen J. et al. CC chemokine receptor 5 polymorphism in rheumatoid arthritis // J. Rheumatol. 1998. № 25. P. 1462—1465.</mixed-citation><mixed-citation xml:lang="en">Garred P., Madsen H., Petersen J. et al. CC chemokine receptor 5 polymorphism in rheumatoid arthritis // J. Rheumatol. 1998. № 25. P. 1462—1465.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Barcellos L.F., Schito A.M., Rimmler J.B. et al. CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis // Immunogenetics. 2000. № 51. P. 281—288.</mixed-citation><mixed-citation xml:lang="en">Barcellos L.F., Schito A.M., Rimmler J.B. et al. CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis // Immunogenetics. 2000. № 51. P. 281—288.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Sellebjerg F., Madsen H.O., Jensen C.V. et al. CCR5 delta32, matrix metalloproteinase-9 and disease activity in multiple sclerosis // J. Neuroimmunol. 2000. № 102 (1). P. 98—106.</mixed-citation><mixed-citation xml:lang="en">Sellebjerg F., Madsen H.O., Jensen C.V. et al. CCR5 delta32, matrix metalloproteinase-9 and disease activity in multiple sclerosis // J. Neuroimmunol. 2000. № 102 (1). P. 98—106.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Balashov K.E., Rottman J.B., Weiner H.L., Hancock W.W. CCR5(+) and CXCR3(+) T cells are increased in multiple sclerosis and their ligands MIP-1alpha and IP-10 are expressed in demyelinating brain lesions // Proc. Natl. Acad. Sci. USA. 1999. № 96 (12). P. 6873—6878.</mixed-citation><mixed-citation xml:lang="en">Balashov K.E., Rottman J.B., Weiner H.L., Hancock W.W. CCR5(+) and CXCR3(+) T cells are increased in multiple sclerosis and their ligands MIP-1alpha and IP-10 are expressed in demyelinating brain lesions // Proc. Natl. Acad. Sci. USA. 1999. № 96 (12). P. 6873—6878.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Trebst C., Staugaitis S.M., Tucky B. et al. Chemokine receptors on infiltrating leucocytes in inflammatory pathologies of the central nervous system (CNS) // Neuropathol. Appl. Neurobiol. 2003. № 29 (6). P. 584—595.</mixed-citation><mixed-citation xml:lang="en">Trebst C., Staugaitis S.M., Tucky B. et al. Chemokine receptors on infiltrating leucocytes in inflammatory pathologies of the central nervous system (CNS) // Neuropathol. Appl. Neurobiol. 2003. № 29 (6). P. 584—595.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Karni A., Balashov K., Hancock W.W. et al. Cyclophosphamide modulates CD4+ T cells into a T helper type 2 phenotype and reverses increased IFN-gamma production of CD8+ T cells in secondary progressive multiple sclerosis // J. Neuroimmunol. 2004. № 146 (1—2). P. 189—198.</mixed-citation><mixed-citation xml:lang="en">Karni A., Balashov K., Hancock W.W. et al. Cyclophosphamide modulates CD4+ T cells into a T helper type 2 phenotype and reverses increased IFN-gamma production of CD8+ T cells in secondary progressive multiple sclerosis // J. Neuroimmunol. 2004. № 146 (1—2). P. 189—198.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Brühl H., Cihak J., Stangassinger M. et al. Depletion of CCR5-expressing cells with bispecific antibodies and chemokine toxins: a new strategy in the treatment of chronic inflammatory diseases and HIV // The Journal of Immunology. 2001. № 166. P. 2420—2426.</mixed-citation><mixed-citation xml:lang="en">Brühl H., Cihak J., Stangassinger M. et al. Depletion of CCR5-expressing cells with bispecific antibodies and chemokine toxins: a new strategy in the treatment of chronic inflammatory diseases and HIV // The Journal of Immunology. 2001. № 166. P. 2420—2426.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Jalonen T.O., Pulkkinen K., Ukkonen M. et al. Differential intracellular expression of CCR5 and chemokines in multiple sclerosis subtypes // J. Neurol. 2002. № 249 (5). P. 576—583.</mixed-citation><mixed-citation xml:lang="en">Jalonen T.O., Pulkkinen K., Ukkonen M. et al. Differential intracellular expression of CCR5 and chemokines in multiple sclerosis subtypes // J. Neurol. 2002. № 249 (5). P. 576—583.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Schreiber K., Otura A.B., Ryder L.P. et al. Disease severity in Danish multiple sclerosis patients evaluated by MRI and three genetic markers (HLA-DRB1*1501, CCR5 deletion mutation, apolipoprotein E) // Mult. Scler. 2002. № 8 (4). P. 295—298.</mixed-citation><mixed-citation xml:lang="en">Schreiber K., Otura A.B., Ryder L.P. et al. Disease severity in Danish multiple sclerosis patients evaluated by MRI and three genetic markers (HLA-DRB1*1501, CCR5 deletion mutation, apolipoprotein E) // Mult. Scler. 2002. № 8 (4). P. 295—298.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Yudin N.S., Vinogradov S.V., Potapova T.A. et al. Distribution of CCR5-delta 32 gene deletion across the Russian part of Eurasia // Hum. Genet. 1998. № 102. P. 695—698.</mixed-citation><mixed-citation xml:lang="en">Yudin N.S., Vinogradov S.V., Potapova T.A. et al. Distribution of CCR5-delta 32 gene deletion across the Russian part of Eurasia // Hum. Genet. 1998. № 102. P. 695—698.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Jagodzinski P.P., Lecybyl R., Ignacak M. et al. Distribution of Δ32 alelle of the CCR5 gene in population of Poland // J. Med. Genet. 2000. № 45. P. 271—274.</mixed-citation><mixed-citation xml:lang="en">Jagodzinski P.P., Lecybyl R., Ignacak M. et al. Distribution of Δ32 alelle of the CCR5 gene in population of Poland // J. Med. Genet. 2000. № 45. P. 271—274.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Ebers G.C., Bulman D. The geography of MS reflects genetic susceptibility // Neurology. 1986. № 36. P. 108.</mixed-citation><mixed-citation xml:lang="en">Ebers G.C., Bulman D. The geography of MS reflects genetic susceptibility // Neurology. 1986. № 36. P. 108.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Sorensen T.L., Tani M., Jensen J. et al. Expression of specific chemokines and chemokine receptors in the central nervous system of multiple sclerosis patients // J. Clin. Invest. 1999. № 103 (6). P. 807—815.</mixed-citation><mixed-citation xml:lang="en">Sorensen T.L., Tani M., Jensen J. et al. Expression of specific chemokines and chemokine receptors in the central nervous system of multiple sclerosis patients // J. Clin. Invest. 1999. № 103 (6). P. 807—815.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Martinson J.J., Chapman N.H., Rees D.C. et al. Global distribution of the CCR5 gene 32-basepair deletion // Nature genetics. 1997. № 16. P. 100—103.</mixed-citation><mixed-citation xml:lang="en">Martinson J.J., Chapman N.H., Rees D.C. et al. Global distribution of the CCR5 gene 32-basepair deletion // Nature genetics. 1997. № 16. P. 100—103.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Haase C.G., Schmidt S., Faustman P.M. Frequencies of the G-protein beta 3 subunit C825T polymorphism and the D32 mutation of the chemokine receptor-5 in patients with multiple sclerosis // Neurosci. Lett. 2002. V. 27. № 330 (3). P. 293—295.</mixed-citation><mixed-citation xml:lang="en">Haase C.G., Schmidt S., Faustman P.M. Frequencies of the G-protein beta 3 subunit C825T polymorphism and the D32 mutation of the chemokine receptor-5 in patients with multiple sclerosis // Neurosci. Lett. 2002. V. 27. № 330 (3). P. 293—295.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Pulkkinen K., Luomala M., Kuusisto H. et al. Increase in CCR5 D32/D32 genotype in multiple sclerosis // Acta Neurol. Scand. 2004. № 109 (5). P. 342—347.</mixed-citation><mixed-citation xml:lang="en">Pulkkinen K., Luomala M., Kuusisto H. et al. Increase in CCR5 D32/D32 genotype in multiple sclerosis // Acta Neurol. Scand. 2004. № 109 (5). P. 342—347.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Silversides J.A., Heggarty S.V., McDonnell G.V. et al. Influence of CCR5 delta32 polymorphism on multiple sclerosis susceptibility and disease course // Multiple Sclerosis. 2004. № 10 (2). P. 149—152.</mixed-citation><mixed-citation xml:lang="en">Silversides J.A., Heggarty S.V., McDonnell G.V. et al. Influence of CCR5 delta32 polymorphism on multiple sclerosis susceptibility and disease course // Multiple Sclerosis. 2004. № 10 (2). P. 149—152.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Balanovsky O., Pocheshkhova E., Pshenichnov A. et al. Is spatial distribution of the HIV-1-Resistant CCR5Δ32 allele formed by ecological factors? // J. of Physiological anthropology and applied human science. 2005. № 24. P. 375—382.</mixed-citation><mixed-citation xml:lang="en">Balanovsky O., Pocheshkhova E., Pshenichnov A. et al. Is spatial distribution of the HIV-1-Resistant CCR5Δ32 allele formed by ecological factors? // J. of Physiological anthropology and applied human science. 2005. № 24. P. 375—382.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kantor R., Bakhanashvili M., Achiron A. A mutated CCR5 gene may have favorable prognostic implications in MS // Neurology. 2003. V. 22. № 61 (2). P. 238—240.</mixed-citation><mixed-citation xml:lang="en">Kantor R., Bakhanashvili M., Achiron A. A mutated CCR5 gene may have favorable prognostic implications in MS // Neurology. 2003. V. 22. № 61 (2). P. 238—240.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Kurtzke J.F., Beebe J.W., Norman J.E. Epidemiology of multiple sclerosis in US veterans. Part I. Race, sex and geographic distribution // Neurology. 1979. № 29. P. 1228—1235.</mixed-citation><mixed-citation xml:lang="en">Kurtzke J.F., Beebe J.W., Norman J.E. Epidemiology of multiple sclerosis in US veterans. Part I. Race, sex and geographic distribution // Neurology. 1979. № 29. P. 1228—1235.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Murphy P.M., Baggiolini M., Charo I.F. et al. Nomenclature for chemokine receptors // Pharmacological reviews. 2001. № 52 (1). P. 1245—1273.</mixed-citation><mixed-citation xml:lang="en">Murphy P.M., Baggiolini M., Charo I.F. et al. Nomenclature for chemokine receptors // Pharmacological reviews. 2001. № 52 (1). P. 1245—1273.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Hvas J., McLean C., Justesen J. Perivascular T cells express the proinflammatory chemokine RANTES mRNA in multiple sclerosis lesions // Scand. J. Immunol. 1997. № 46. P. 195—203.</mixed-citation><mixed-citation xml:lang="en">Hvas J., McLean C., Justesen J. Perivascular T cells express the proinflammatory chemokine RANTES mRNA in multiple sclerosis lesions // Scand. J. Immunol. 1997. № 46. P. 195—203.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Sadovnick A.D., Ebers G.C. Epidemiology of multiple sclerosis: a critical overview // Can. J. Neurol. Sci. 1993. № 20 (1). P. 17—29.</mixed-citation><mixed-citation xml:lang="en">Sadovnick A.D., Ebers G.C. Epidemiology of multiple sclerosis: a critical overview // Can. J. Neurol. Sci. 1993. № 20 (1). P. 17—29.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Sallusto F., Lanzavecchia A., Mackay C.R. Chemokines and chemokine receptors in T-cell priming and Th1/Th2-mediated responses // Immunol. Today. 1998. № 19. P. 568—574.</mixed-citation><mixed-citation xml:lang="en">Sallusto F., Lanzavecchia A., Mackay C.R. Chemokines and chemokine receptors in T-cell priming and Th1/Th2-mediated responses // Immunol. Today. 1998. № 19. P. 568—574.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Bennetts B.H., Teutsch S.M., Buhler M.M. et al. The CCR deletion mutation fails to protect against multiple sclerosis // Hum Immunology. 1997. № 58 (1). P. 52—59.</mixed-citation><mixed-citation xml:lang="en">Bennetts B.H., Teutsch S.M., Buhler M.M. et al. The CCR deletion mutation fails to protect against multiple sclerosis // Hum Immunology. 1997. № 58 (1). P. 52—59.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Favorova O.O., Andreewski T.V., Boiko A.N. et al. The chemokine receptor CCR5 deletion mutation is associated with MS in HLA-DR4-positive Russians // Neurology. 2002. № 59. P. 1652—1655.</mixed-citation><mixed-citation xml:lang="en">Favorova O.O., Andreewski T.V., Boiko A.N. et al. The chemokine receptor CCR5 deletion mutation is associated with MS in HLA-DR4-positive Russians // Neurology. 2002. № 59. P. 1652—1655.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Trebst C., Ransohoff R.M. Investigating chemokines and chemokine receptors in patients with multiple sclerosis: opportunities and challenges // Arch. Neurol. 2001. № 58. P. 1975—1980.</mixed-citation><mixed-citation xml:lang="en">Trebst C., Ransohoff R.M. Investigating chemokines and chemokine receptors in patients with multiple sclerosis: opportunities and challenges // Arch. Neurol. 2001. № 58. P. 1975—1980.</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>
