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    Academic Journal

    Contributors: Настоящее исследование выполнено в рамках фундаментальной темы № 1021051402790-6 «Изучение иммунопатологии, диагностики и терапии на ранних стадиях системных ревматических заболеваний».

    Source: Rheumatology Science and Practice; Vol 61, No 1 (2023); 100-105 ; Научно-практическая ревматология; Vol 61, No 1 (2023); 100-105 ; 1995-4492 ; 1995-4484

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    Relation: https://rsp.mediar-press.net/rsp/article/view/3285/2263; Goldblatt F, O’Neill SG. Clinical aspects of autoimmune rheumatic diseases. Lancet. 2013;382(9894):797-808. doi:10.1016/S0140-6736(13)61499-3; Davidson A, Diamond B. Autoimmune diseases. N Engl J Med. 2001;345(5):340-350. doi:10.1056/NEJM200108023450506; Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997;40(9):1725. doi:10.1002/art.1780400928; Petri M, Orbai AM, Alarcón GS, Gordon C, Merrill JT, Fortin PR, et al. Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus. Arthritis Rheum. 2012;64(8):2677-2686. doi:10.1002/art.34473; Aringer M, Costenbader K, Daikh D, Brinks R, Mosca M, Ramsey-Goldman R, et al. 2019 European League Against Rheumatism/American College of Rheumatology classification criteria for systemic lupus erythematosus. Ann Rheum Dis. 2019;78(9): 1151-1159. doi:10.1136/annrheumdis-2018-214819; van den Hoogen F, Khanna D, Fransen J, Johnson SR, Baron M, Tyndall A, et al. 2013 classification criteria for systemic sclerosis: An American college of Rheumatology/European League Against Rheumatism collaborative initiative. Ann Rheum Dis. 2013;72(11):1747-1755. doi:10.1136/annrheumdis-2013-204424; Shiboski SC, Shiboski CH, Criswell L, Baer A, Challacombe S, Lanfranchi H, et al.; Sjögren’s International Collaborative Clinical Alliance (SICCA) Research Groups. American College of Rheumatology classification criteria for Sjögren’s syndrome: A datadriven, expert consensus approach in the Sjögren’s International Collaborative Clinical Alliance cohort. Arthritis Care Res (Hoboken). 2012;64(4):475-487. doi:10.1002/acr.21591; Arbuckle MR, McClain MT, Rubertone MV, Scofield RH, Dennis GJ, James JA, et al. Development of autoantibodies before the clinical onset of systemic lupus erythematosus. N Engl J Med. 2003;349(16):1526-1533. doi:10.1056/NEJMoa021933; Eriksson C, Kokkonen H, Johansson M, Hallmans G, Wadell G, Rantapää-Dahlqvist S. Autoantibodies predate the onset of systemic lupus erythematosus in northern Sweden. Arthritis Res Ther. 2011;13(1):R30. doi:10.1186/ar3258; Насонов ЕЛ, Соловьев СК, Арш инов АВ. Системная красная волчанка: история и современность. Научно-практическая ревматология. 2022;60(4):397-412. doi:10.47360/1995-4484-2022-397-412; Насонов ЕЛ, Попкова ТВ, Панафидина ТА. Проблемы ранней диагностики системной красной волчанки в период пандемии COVID-19. Научно-практическая ревматология. 2021;59(2):119-128. doi:10.47360/1995-4484-2021-119-128; Lambers WM, Westra J, Jonkman MF, Bootsma H, de Leeuw K. Incomplete systemic lupus erythematosus – what remains after application of ACR and SLICC criteria? Arthritis Care Res. 2020;72(5):607-614. doi:10.1002/acr.23894; Насонов ЕЛ (ред.). Ревматология. Российские клинические рекомендации. М.:ГЭОТАР-Медиа;2017.; Agmon-Levin N, Damoiseaux J, Kallenberg C, Sack U, Witte T, Herold M, et al. International recommendations for the assessment of autoantibodies to cellular antigens referred to as anti-nuclear antibodies. Ann Rheum Dis. 2014;73(1):17-23. doi:10.1136/annrheumdis-2013-203863; Solomon DH, Kavanaugh AJ, Schur PH. American College of Rheumatology Ad Hoc Committee on Immunologic Testing guidelines. Evidence-based guidelines for the use of immunologic tests: Antinuclear antibody testing. Arthritis Rheum. 2002;47(4):434-444. doi:10.1002/art.10561; Александрова ЕН, Верижникова ЗГ, Новиков АА, Лукина ГВ. Современный взгляд на проблемы исследования антинуклеарных антител при системной красной волчанке (обзор литературы). Клиническая лабораторная диагностика. 2018;63(6):340-348. doi:10.18821/0869-2084-2018-63-6-340-348; Kang SY, Lee WI, Kim MH, La Jeon Y. Clinical use of antiDFS70 autoantibodies. Rheumatol Int. 2019;39(8):1423-1429. doi:10.1007/s00296-019-04299-4; Насонов ЕЛ, Александрова ЕН, Новиков АА. Аутоиммунные ревматические болезни – проблемы иммунопатологии и персонифицированного лечения. Анналы Российской академии медицинских наук. 2015;70(2):169-182. doi:10.15690/vramn.v70i2.1310; Carter JB, Carter S, Saschenbrecker S, Goeckeritz BE. Recognition and relevance of Anti-DFS70 autoantibodies in routine antinuclear autoantibodies testing at a community hospital. Front Med (Lausanne). 2018;5:88. doi:10.3389/fmed.2018.00088; Basu A, Sanchez TW, Casiano CA. DFS70/LEDGFp75: An enigmatic autoantigen at the interface between autoimmunity, AIDS, and cancer. Front Immunol. 2015;6:116. doi:10.3389/fimmu.2015.00116; Pisetsky DS. Antinuclear antibody testing – misunderstood or misbegotten? Nat Rev Rheumatol. 2017;13(8):495-502. doi:10.1038/nrrheum.2017.74; Pascolini S, Vannini A, Deleonardi G, Ciordinik M, Sensoli A, Carletti I, et al. COVID-19 and immunological dysregulation: Can autoantibodies be useful? Clin Transl Sci. 2021;14(2):502-508. doi:10.1111/cts.12908; Gazzaruso C, Carlo Stella N, Mariani G, Nai C, Coppola A, Naldani D, et al. High prevalence of antinuclear antibodies and lupus anticoagulant in patients hospitalized for SARS-CoV2 pneumonia. Clin Rheumatol. 2020;39(7):2095-2097. doi:10.1007/s10067-020-05180-7; Vlachoyiannopoulos PG, Magira E, Alexopoulos H, Jahaj E, Theophilopoulou K, Kotanidou A, et al. Autoantibodies related to systemic autoimmune rheumatic diseases in severely ill patients with COVID-19. Ann Rheum Dis. 2020;79(12):1661-1663. doi:10.1136/annrheumdis-2020-218009; Sacchi MC, Tamiazzo S, Stobbione P, Agatea L, De Gaspari P, Stecca A, et al. SARS-CoV-2 infection as a trigger of autoimmune response. Clin Transl Sci. 2021;14(3):898-907. doi:10.1111/cts.12953; Насонов ЕЛ, Самсонов МЮ, Лила АМ. Коронавирусная болезнь 2019 (COVID-19) и аутоиммунитет. Вестник Российской академии наук. 2022;92(7):654-660. doi:10.31857/S086958732207012X; Mahler M, Fritzler MJ. The clinical significance of the dense fine speckled immunofluorescence pattern on HEp-2 cells for the diagnosis of systemic autoimmune diseases. Clin Dev Immunol. 2012;2012:494356. doi:10.1155/2012/494356; Conrad K, Röber N, Andrade LE, Mahler M. The clinical relevance of anti-DFS70 autoantibodies. Clin Rev Allergy Immunol. 2017;52(2):202-216. doi:10.1007/s12016-016-8564-5; Ochs RL, Stein TW Jr, Peebles CL, Gittes RF, Tan EM. Autoantibodies in interstitial cystitis. J Urol. 1994;151(3):587-592. doi:10.1016/s0022-5347(17)35023-1; Conrad K, Andrade LE, Chan EK, Mahler M, Meroni PL, Pruijn GJ, et al. From autoantibody research to standardized diagnostic assays in the management of human diseases – Report of the 12th Dresden Symposium on Autoantibodies. Lupus. 2016;25(8):787-796. doi:10.1177/0961203316644337; Damoiseaux J, Andrade LEC, Carballo OG, Conrad K, Francescantonio PLC, Fritzler MJ, et al. Clinical relevance of HEp-2 indirect immunofluorescent patterns: The International Consensus on ANA patterns (ICAP) perspective. Ann Rheum Dis. 2019;78(7):879-889. doi:10.1136/annrheumdis-2018-214436; Chan EK, Damoiseaux J, Carballo OG, Conrad K, de Melo Cruvinel W, Francescantonio PL, et al. Report of the First International Consensus on standardized nomenclature of antinuclear antibody HEp-2 cell patterns 2014–2015. Front Immunol. 2015;6:412. doi:10.3389/fimmu.2015.00412; Mahler M, Parker T, Peebles CL, Andrade LE, Swart A, Carbone Y, et al. Anti-DFS70/LEDGF antibodies are more prevalent in healthy individuals compared to patients with systemic autoimmune rheumatic diseases. J Rheumatol. 2012;39(11):2104-2110. doi:10.3899/jrheum.120598; Bizzaro N, Pesente F, Cucchiaro F, Infantino M, Tampoia M, Villalta D, et al. Anti-DFS70 antibodies detected by immunoblot methods: A reliable tool to confirm the dense fine speckles ANA pattern. J Immunol Methods. 2016;436:50-53. doi:10.1016/j.jim.2016.06.008; Malyavantham K, Suresh L. Analysis of DFS70 pattern and impact on ANA screening using a novel HEp-2 ELITE/DFS70 knockout substrate. Autoimmun Highlights. 2017;8(1):3. doi:10.1007/s13317-017-0091-8; Dellavance A, Viana VS, Leon EP, Bonfa ES, Andrade LE, Leser PG. The clinical spectrum of antinuclear antibodies associated with the nuclear dense fine speckled immunofluorescence pattern. J Rheumatol. 2005;32(11):2144-2149.; Ochs RL, Muro Y, Si Y, Ge H, Chan EK, Tan EM. Autoantibodies to DFS70kd/transcription coactivator p75 in atopic dermatitis and other conditions. J Allergy Clin Immunol. 2000;105(6 Pt 1):1211-1220. doi:10.1067/mai.2000.107039; Ochs RL, Mahler M, Basu A, Rios-Colon L, Sanchez TW, Andrade LE, et al. The significance of autoantibodies to DFS70/LEDGFp75 in health and disease: integrating basic science with clinical understanding. Clin Exp Med. 2016;16(3):273-293. doi:10.1007/s10238-015-0367-0; Okamoto M, Ogawa Y, Watanabe A, Sugiura K, Shimomura Y, Aoki N, et al. Autoantibodies to DFS70/LEDGF are increased in alopecia areata patients. J Autoimmun. 2004;23(3):257-266. doi:10.1016/j.jaut.2004.07.004; Daniels T, Zhang J, Gutierrez I, Elliot ML, Yamada B, Heeb MJ, et al. Antinuclear autoantibodies in prostate cancer: immunity to LEDGF/p75, a survival protein highly expressed in prostate tumors and cleaved during apoptosis. Prostate. 2005;62(1):14-26. doi:10.1002/pros.20112; Ortiz-Hernandez GL, Sanchez-Hernandez ES, Casiano CA. Twenty years of research on the DFS70/LEDGF autoantibody-autoantigen system: Many lessons learned but still many questions. Auto Immun Highlights. 2020;11(1):3. doi:10.1186/s13317-020-0126-4; Александрова ЕН, Верижникова ЖГ, Новиков АА, Панафидина ТА, Попкова ТВ. Антитела к DFS70 – новый биомаркер для исключения диагноза системной красной волчанки у АНФ-позитивных здоровых лиц. Научно-практическая ревматология. 2017;55(2 Прил 1):8.; Александрова ЕН, Новиков АА, Клюквина НГ, Васильев ВИ, Лукина ГВ. Диагностическое значение моноспецифических антител к DFS70 при системных аутоиммунных ревматических заболеваниях. Медицинский алфавит. 2021(33):38-41. doi:10.33667/2078-5631-2021-33-38-41; Ganapathy V, Casiano CA. Autoimmunity to the nuclear autoantigen DFS70 (LEDGF): What exactly are the autoantibodies trying to tell us? Arthritis Rheum. 2004;50(3):684-688. doi:10.1002/art.20095; Miyara M, Albesa R, Charuel JL, El Amri M, Fritzler MJ, Ghillani-Dalbin P, et al. Clinical phenotypes of patients with antiDFS70/LEDGF antibodies in a routine ANA referral cohort. Clin Dev Immunol. 2013;2013:703759. doi:10.1155/2013/703759; Mariz HA, Sato EI, Barbosa SH, Rodrigues SH, Dellavance A, Andrade LE. Pattern on the antinuclear antibody-HEp-2 test is a critical parameter for discriminating antinuclear antibody-positive healthy individuals and patients with autoimmune rheumatic diseases. Arthritis Rheum. 2011;63(1):191-200. doi:10.1002/art.30084; Watanabe A, Kodera M, Sugiura K, Usuda T, Tan EM, Takasaki Y, et al. Anti-DFS70 antibodies in 597 healthy hospital workers. Arthritis Rheum. 2004;50(3):892-900. doi:10.1002/art.20096; Schmeling H, Mahler M, Levy DM, Moore K, Stevens AM, Wick J, et al. Autoantibodies to dense fine speckles in pediatric diseases and controls. J Rheumatol. 2015;42(12):2419-2426. doi:10.3899/jrheum.150567; Peker BO, Şener AG, Tarhan EF, Kaya S. Investigation of antiDFS70 antibody in patients with systemic autoimmune rheumatic diseases. Clin Rheumatol. 2019;(38):3627-3633. doi:10.1007/s10067-019-04730-y; Choi MY, Clarke AE, St Pierre Y, Hanly JG, Urowitz MB, Romero-Diaz J, et al. The prevalence and determinants of anti-DFS70 autoantibodies in an international inception cohort of systemic lupus erythematosus patients. Lupus. 2017;26(10):1051-1059. doi:10.1177/0961203317692437; Muro Y, Sugiura K, Nakashima R, Mimori T, Akiyama M. Low prevalence of anti-DFS70/LEDGF antibodies in patients with dermatomyositis and other systemic autoimmune rheumatic diseases. J Rheumatol. 2013;40(1):92-93. doi:10.3899/jrheum.121168; Infantino M, Carbone T, Manfredi M, Grossi V, Benucci M, Blank M, et al. Are anti-DFS70 autoantibodies protective? Isr Med Assoc J. 2019;21(8):509-511.; Infantino M, Shovman O, Pérez D, Manfredi M, Grossi V, Benucci M, et al. Anti-DFS70 autoantibodies in undifferentiated connective tissue diseases subjects: What’s on the horizon? Rheumatology (Oxford). 2018;57(7):1293-1298. doi:10.1093/rheumatology/key012; Aljadeff G, Shemer A, Katz I, Andrade LEC, Gilburd B, Halpert G, et al. Infusion of anti-DFS70 antibodies prolonged survival of lupus-prone mice. Lupus. 2021;30(2):320-324. doi:10.1177/0961203320969976

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    Academic Journal

    Source: CHILDREN INFECTIONS; Том 16, № 4 (2017); 36-41 ; ДЕТСКИЕ ИНФЕКЦИИ; Том 16, № 4 (2017); 36-41 ; 2618-8139 ; 2072-8107 ; 10.22627/2072-8107-2017-16-4

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    Relation: https://detinf.elpub.ru/jour/article/view/324/313; Зверева Н.Н., Шакарян А.К., Сайфуллин Р.Ф., Россина А.Л., Ртищев А.Ю., Белялетдинова И.Х. Современное состояние проблемы иксодового клещевого боррелиоза (болезни Лайма) у детей. Детские инфекции. 2017;16(1):27—31. DOI:10.22627/2072-8107-2017-16-1-27-31 [Zvereva N.N., Shakaryan K., Sayfullin R.F., Rossina A.L., Rtishchev Y., Belyaletdinovа K. Сurrent status of the problem of ixodic tickborne borreliosis (Lyme disease) in children. Detskie Infektsii=Children's infections. 2017;16(1):27—31. (In Russ.) DOI:10.22627/2072-8107-2017-16-1-27-31]; Егорова Т. В., Малкова Л. В., Рябова Н. В. Клиническое значе- ние динамики титров антител к боррелиям у детей с болезнью Лайма. Детские Инфекции. 2007; 6(2): 69—73. [Egorova T. V., Malkova L. V., Ryabova N. V. Clinical significance of dynamics of antybody titers against borrelia in children from Lyme’s disease. Detskie Infektsii=Children's infections. 2007; 6(2): 69—73. (In Russ).]; Скрипченко Н. В. Балинова А. А. Современные представления о патогенезе иксодовых клещевых боррелиозов. Журнал Инфектологии. 2012; 4(2): 5—15. [Skripchenko N. V. Balinova A. A. Modern conception about ixodes tike-born borreliosis. Zhurnal Infektologii=Journal of Infectology 2012; 4(2): 5—15 (In Russ).]; Егорова Т. В., Стражникова Г.А., Вожегова Н.П. К вопросу об ассоциации болезни Лайма у детей с антигенами главного комплекса гистосовместимости. Сборник научных статей «Актуальные проблемы современной клинической медицины». Омск, 2006: 12—19. [Egorova T. V., Strazhnikova G.A., Vozhegova N.P. To the question about association of Lyme disease and HLA in children. Collection of scientific articles «Actual problems of modern clinical medicine». Omsk, 2006: 12—19. (In Russ).]; Скрипченко Н. В., Иванова Г. П., Трофимова Т. Н., Мурина Е. А. Роль инфекционного и возрастного фактора в развитии лейкоэнцефалитов у детей. Журнал Инфектологии. 2010; 2(2): 54—61. [Skripchenko N. V., Ivanova G. P., Trofimova T. N., Murina E. A. The role of the infectious and age factor in the development of leukoencephalitis in children. Zhurnal Infektologii=Journal of Infectology. 2010; 2(2): 54—61. (In Russ).]; Скрипченко Н.В., Старшинов Я.Ю., Трофимова Т. Н., В. В. Иванова и др. Диссеминированные энцефаломиелиты у детей: диагностика, клиника, лечение, диспансеризация: Методические рекомендации. СПб., 2004: 60. [Skripchenko N.V., Starshinov Ya.Yu., Trofimova T. N., Ivanova V. V. et al. Disseminated encephalomyelitis in children: diagnosis, clinical picture, treatment, prophylactic medical examination. SPb., 2004:60. (In Russ).]; https://detinf.elpub.ru/jour/article/view/324

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