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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">rsp</journal-id><journal-title-group><journal-title xml:lang="ru">Научно-практическая ревматология</journal-title><trans-title-group xml:lang="en"><trans-title>Rheumatology Science and Practice</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1995-4484</issn><issn pub-type="epub">1995-4492</issn><publisher><publisher-name>IMA-PRESS, LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/1995-4484-2002-741</article-id><article-id custom-type="elpub" pub-id-type="custom">rsp-878</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>Статьи</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>Articles</subject></subj-group></article-categories><title-group><article-title>КЛИНИЧЕСКОЕ ЗНАЧЕНИЕ ИНТЕРЛЕЙКИНА-4 ПРИ СИСТЕМНОЙ СКЛЕРОДЕРМИИ</article-title><trans-title-group xml:lang="en"><trans-title>CLINICAL IMPORTANCE OF INTERLEUKIN-4 IN SYSTEMIC SCLERODERMA</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>Невская</surname><given-names>Т. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Nevskaya</surname><given-names>T A</given-names></name></name-alternatives><email xlink:type="simple">-</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Ryazanlzeva</surname><given-names>T A</given-names></name><name name-style="western" xml:lang="en"><surname>Ryazanlzeva</surname><given-names>T A</given-names></name></name-alternatives><email xlink:type="simple">-</email></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гусева</surname><given-names>Н. Г.</given-names></name><name name-style="western" xml:lang="en"><surname>Guseva</surname><given-names>N G</given-names></name></name-alternatives><email xlink:type="simple">-</email></contrib></contrib-group><pub-date pub-type="collection"><year>2002</year></pub-date><pub-date pub-type="epub"><day>15</day><month>02</month><year>2002</year></pub-date><volume>40</volume><issue>1</issue><issue-title>№1 (2002)</issue-title><fpage>9</fpage><lpage>13</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Невская Т.А., Ryazanlzeva T.A., Гусева Н.Г., 2002</copyright-statement><copyright-year>2002</copyright-year><copyright-holder xml:lang="ru">Невская Т.А., Ryazanlzeva T.A., Гусева Н.Г.</copyright-holder><copyright-holder xml:lang="en">Nevskaya T.A., Ryazanlzeva T.A., Guseva N.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://rsp.mediar-press.net/rsp/article/view/878">https://rsp.mediar-press.net/rsp/article/view/878</self-uri><abstract><p>Цель. Изучить взаимосвязь сывороточного уровня интерлейкина-4 (ИЛ-4) с висцеральной патологией, характером течения и клиническими формами ССД. Материалы и методы. ИЛ-4 определялся в сыворотках 40 больных ССД непрямым твердофазным имму- нофермеитным методом (ELISA). Результаты. Уровень ИЛ-4 в пределах Ю-ЮООпг/мл выявлен у 12 из 40 больных ССД (30%). Отличительными особенностями этой группы больных были меньшая длительность заболевания, прогрессирование кожного фиброза и висцеральной патологии к моменту обследования и тенденция к большей частоте легочного фиброза. Существенных различий в поражении других внутренних органов, как и зависимости содержания ИЛ-4 от клинических форм и течения заболевания, выявлено не было. У больных с повышением ИЛ-4 в крови отмечены более высокие уровни ЦИК, у-глобулинов, в то время как содержание острофазовых реактантов было ниже, чем в остальной группе. Вывод. Установленная связь сывороточного уровня ИЛ-4 с активностью фиброзного процесса при ССД требует подтверждения в проспективных исследованиях.</p></abstract><trans-abstract xml:lang="en"><p>The aim of the study was to investigate whether serum levels of interleukin-4 ( IL-4) reflects the clinical disease status and laboratory features of systemic sclerosis (SSc). IL-4 was measured by ELISA in forty patients wilh SSc. We revealed IL-4 (Ю-lOOOpg/ml) in sera from 12 of 40 pts (30%). These pts had significantly less duration of disease, the progression of skin and visceral involvement by the time of investigation and a trend lo the greater frequency of lung fibrosis. There was no correlation of IL-4 level with type of SSc. The pts with increased scrum levels of IL-4 had higher levels of circulated immune complexes, y-globulins, but the levels of acute phase reactants (CRP, fibrinogen) were lower compared with the of others. We suggest that serum IL-4 may serve a biologic marker for the progression of skin and lung fibrosis, but the results require confirmation in longitudinal study.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>интерлейкин-4</kwd><kwd>системная склеродермия</kwd><kwd>Т лимфоциты</kwd><kwd>фиброз</kwd><kwd>активность</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">&lt;div&gt;&lt;p&gt;Atamas S.P., Yurovsky V.V., Wise R. Production of type 2 cytokines by CD8’ lung cclls is associated with greater decline in pulmonary function in patients with systemic sclcrosis. Arihr, Rheum., 1999, 42(6), 1168-78.&lt;/p&gt;&lt;p&gt;Ihn H„ Sato S., Fujimoto M. Demonstration of interleukin-2. interleukin-4 and interleukin-6 in sera from patients with localized scleroderma. Arch. Dermatol. Res., 1995, 287(2), 193-7,&lt;/p&gt;&lt;p&gt;Fertin C., Nicolas J.F., Gillcry P. Interleukin-4 stimulates collagen synthesis by normal and scleroderma fibroblasts in dermal equivalents. Cell. Mol. Biol., 1991, 37(8), 823-829.&lt;/p&gt;&lt;p&gt;Korn J.H. Systemic sclcrosis: current pathogenetic concepts and I'uture prospects for targeted therapy. Lancet., 1996, 347, 1455.&lt;/p&gt;&lt;p&gt;Kuroda K„ Shinkai H, Downregulatcd of decorin expression in dermal fibroblasts by interleukin-4. Arch. Dermatol. Res. 1997, 289, 476-480.&lt;/p&gt;&lt;p&gt;Lee K.S., Ro Y.J., Ryoo Y.W,, Kwon H.S. Regulation of intcr- leukin-4 on collagen gene expression in systemic sclerosis fibroblast culture.I. Dermatol. Sci„ 1996, 12(2), 110-117.&lt;/p&gt;&lt;p&gt;Needleman B.W., Fredrick M.W., Stair R.W. Interleukin-!, interleukin-2, interleukin-4, interleukin-6, tumor necrosis fac- lor a, and interferon-7 levels in sera from patients with scleroderma. Arthr. Rheum., 1992, 35(1), 67-72.&lt;/p&gt;&lt;p&gt;Ong C., Wong C., Roberts C.R., Teh H.S. Anti-IL-4 treatment prevents dermal collagen deposition in the light-skin mouse model of scleroderma. Eur. J. Immunol., 1998, 28(9). 26192629.&lt;/p&gt;&lt;p&gt;Picla-Stnilh Т.Н. Broketa G., Hand A., Korn J.H. Regulation of ICAM-I expression and function in human dermal fibroblasts by 1L-4. J. оГ Immunol., 1996, 145(5), 1375-1381.&lt;/p&gt;&lt;p&gt;Postlethwaits A.E. Role of T cells and cytokines in effecting fibrosis. Int. Rev. Immunol., 1995, 12(2-4), 247-258.&lt;/p&gt;&lt;p&gt;Salmon-Ehr V., Serpier H„ Nawrocki B. Expression of 1L-4 in scleroderma skin speciemeius and scleroderma fibroblast cultures. Potential role in fibrosis. Arch. Dermatol., 1996, 132(7), 802-806.&lt;/p&gt;&lt;p&gt;Sakkas L.I., Touriellolle Ch., Berney.1, Increased levels of alternatively spliced interleukin 4 (IL-4) transcripts in peripheral blood mononuclear cells from palients with systemic sclerosis. Clin, and Diagn. Lab. Immunology., 1999, 6(5), 660-664.&lt;/p&gt;&lt;p&gt;Serpier H., Gillery P., Salmon-Ehr V. Antagonistic effects of inlerferon-gamma and interleukin-4 on fibroblast cultures. J of Invest. Dermatology, 1997, 109, 158-162.&lt;/p&gt;&lt;p&gt;Szegedi A., Czirjak L., Unkeless J.C. Serum cytokine and nnti-FC gamma R autoantibody measurements in patients wilh systemic sclerosis. Acta. Derm. Venerol,, 1996, 76(1), 21-23.&lt;/p&gt;&lt;p&gt;Trojanowska M„ Le Roy E.C., Kekes B. and Kreig Th.Patho genesis of fibrosis: type I collagen and the skin. J. Mol. Med.,1998, 76, 266-274.&lt;/p&gt;&lt;p&gt;Y oshikaw a H., N akajim a Y., T asak a K. G lucocorticoid supress autocrine survival of mast cells by inhibiting IL-4 produc tion and ICAM-1 expression. J.Immunol., 1999, 162(10), 6162-6170.&lt;/p&gt;&lt;/div&gt;&lt;br /&gt;</mixed-citation><mixed-citation xml:lang="en">&lt;div&gt;&lt;p&gt;Atamas S.P., Yurovsky V.V., Wise R. Production of type 2 cytokines by CD8’ lung cclls is associated with greater decline in pulmonary function in patients with systemic sclcrosis. Arihr, Rheum., 1999, 42(6), 1168-78.&lt;/p&gt;&lt;p&gt;Ihn H„ Sato S., Fujimoto M. Demonstration of interleukin-2. interleukin-4 and interleukin-6 in sera from patients with localized scleroderma. Arch. Dermatol. Res., 1995, 287(2), 193-7,&lt;/p&gt;&lt;p&gt;Fertin C., Nicolas J.F., Gillcry P. Interleukin-4 stimulates collagen synthesis by normal and scleroderma fibroblasts in dermal equivalents. Cell. Mol. Biol., 1991, 37(8), 823-829.&lt;/p&gt;&lt;p&gt;Korn J.H. Systemic sclcrosis: current pathogenetic concepts and I'uture prospects for targeted therapy. Lancet., 1996, 347, 1455.&lt;/p&gt;&lt;p&gt;Kuroda K„ Shinkai H, Downregulatcd of decorin expression in dermal fibroblasts by interleukin-4. Arch. Dermatol. Res. 1997, 289, 476-480.&lt;/p&gt;&lt;p&gt;Lee K.S., Ro Y.J., Ryoo Y.W,, Kwon H.S. Regulation of intcr- leukin-4 on collagen gene expression in systemic sclerosis fibroblast culture.I. Dermatol. Sci„ 1996, 12(2), 110-117.&lt;/p&gt;&lt;p&gt;Needleman B.W., Fredrick M.W., Stair R.W. Interleukin-!, interleukin-2, interleukin-4, interleukin-6, tumor necrosis fac- lor a, and interferon-7 levels in sera from patients with scleroderma. Arthr. Rheum., 1992, 35(1), 67-72.&lt;/p&gt;&lt;p&gt;Ong C., Wong C., Roberts C.R., Teh H.S. Anti-IL-4 treatment prevents dermal collagen deposition in the light-skin mouse model of scleroderma. Eur. J. Immunol., 1998, 28(9). 26192629.&lt;/p&gt;&lt;p&gt;Picla-Stnilh Т.Н. Broketa G., Hand A., Korn J.H. Regulation of ICAM-I expression and function in human dermal fibroblasts by 1L-4. J. оГ Immunol., 1996, 145(5), 1375-1381.&lt;/p&gt;&lt;p&gt;Postlethwaits A.E. Role of T cells and cytokines in effecting fibrosis. Int. Rev. Immunol., 1995, 12(2-4), 247-258.&lt;/p&gt;&lt;p&gt;Salmon-Ehr V., Serpier H„ Nawrocki B. Expression of 1L-4 in scleroderma skin speciemeius and scleroderma fibroblast cultures. Potential role in fibrosis. Arch. Dermatol., 1996, 132(7), 802-806.&lt;/p&gt;&lt;p&gt;Sakkas L.I., Touriellolle Ch., Berney.1, Increased levels of alternatively spliced interleukin 4 (IL-4) transcripts in peripheral blood mononuclear cells from palients with systemic sclerosis. Clin, and Diagn. Lab. Immunology., 1999, 6(5), 660-664.&lt;/p&gt;&lt;p&gt;Serpier H., Gillery P., Salmon-Ehr V. Antagonistic effects of inlerferon-gamma and interleukin-4 on fibroblast cultures. J of Invest. Dermatology, 1997, 109, 158-162.&lt;/p&gt;&lt;p&gt;Szegedi A., Czirjak L., Unkeless J.C. Serum cytokine and nnti-FC gamma R autoantibody measurements in patients wilh systemic sclerosis. Acta. Derm. Venerol,, 1996, 76(1), 21-23.&lt;/p&gt;&lt;p&gt;Trojanowska M„ Le Roy E.C., Kekes B. and Kreig Th.Patho genesis of fibrosis: type I collagen and the skin. J. Mol. Med.,1998, 76, 266-274.&lt;/p&gt;&lt;p&gt;Y oshikaw a H., N akajim a Y., T asak a K. G lucocorticoid supress autocrine survival of mast cells by inhibiting IL-4 produc tion and ICAM-1 expression. J.Immunol., 1999, 162(10), 6162-6170.&lt;/p&gt;&lt;/div&gt;&lt;br /&gt;</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>
