المؤلفون: S. S. Benevolenskaya, I. V. Kudriavtsev, M. K. Serebriakova, I. N. Grigor’yeva, E. S. Kuvardin, A. I. Budkova, S. V. Koniakhin, D. B. Zammoeva, D. B. Motorin, A. Yu. Zaritskey, I. Z. Gaydukova, E. K. Gaydukova, S. V. Lapin, A. L. Maslyanskiy, С. С. Беневоленская, И. В. Кудрявцев, М. К. Серебрякова, И. Н. Григорьева, Е. С. Кувардин, А. И. Будкова, С. В. Коняхин, Д. Б. Заммоева, Д. Б. Моторин, А. Ю. Зарицкий, И. З. Гайдукова, Е. К. Гайдукова, С. В. Лапин, А. Л. Маслянский

المساهمون: Исследование выполнено при финансовой поддержке Министерства науки и высшего образования Российской Федерации (соглашение № 075-15-2022-301 от 20.04.2022)

المصدر: Rheumatology Science and Practice; Vol 62, No 5 (2024); 501-512 ; Научно-практическая ревматология; Vol 62, No 5 (2024); 501-512 ; 1995-4492 ; 1995-4484

مصطلحات موضوعية: проточная цитометрия, B cells, systemic lupus erythematosus, primary Sjogren’s syndrome, flow cytometry, В-лимфоциты, системная красная волчанка, болезнь Шегрена

وصف الملف: application/pdf

Relation: https://rsp.mediar-press.net/rsp/article/view/3636/2404; Насонов ЕЛ (ред.). Ревматология. Российские клинические рекомендации. М.:ГЭОТАР-Медиа;2017.; Pasoto SG, Adriano de Oliveira Martins V, Bonfa E. Sjögren’s syndrome and systemic lupus erythematosus: Links and risks. Open Access Rheumatol. 2019;11:33-45. doi:10.2147/OARRR.S167783; Ambrus JL, Suresh L, Peck A. Multiple roles for B-lymphocytes in Sjogren’s syndrome. J Clin Med. 2016;5(10):87. doi:10.3390/jcm5100087; Groom J, Kalled SL, Cutler AH, Olson C, Woodcock SA, Schneider P, et al. Association of BAFF/BLyS overexpression and altered B cell differentiation with Sjögren’s syndrome. J Clin Invest. 2002;109(1):59-68. doi:10.1172/JCI14121; Nocturne G, Seror R, Fogel O, Belkhir R, Boudaoud S, Saraux A, et al. CXCL13 and CCL11 serum levels and lymphoma and disease activity in primary Sjögren’s syndrome. Arthritis Rheumatol. 2015;67(12):3226-3233. doi:10.1002/art.39315; Carvajal Alegria G, Gazeau P, Hillion S, Daïen CI, Cornec DYK. Could lymphocyte profiling be useful to diagnose systemic autoimmune diseases? Clin Rev Allergy Immunol. 2017;53(2):219-236. doi:10.1007/s12016-017-8608-5; Aringer M, Costenbader K, Daikh D, Brinks R, Mosca M, Ramsey-Goldman R, Smolen JS, et al. 2019 European League Against Rheumatism/American College of Rheumatology classification criteria for systemic lupus erythematosus. Arthritis Rheumatol. 2019;71(9):1400-1412. doi:10.1002/art.40930; Shiboski CH, Shiboski SC, Seror R, Criswell LA, Labetoulle M, Lietman TM, et al.; International Sjögren’s Syndrome Criteria Working Group. 2016 American College of Rheumatology/European League Against Rheumatism classification criteria for primary Sjögren’s syndrome: A consensus and data-driven methodology involving three international patient cohorts. Arthritis Rheumatol. 2017;69(1):35-45. doi:10.1002/art.39859; Petri M, Kim MY, Kalunian KC, Grossman J, Hahn BH, Sammaritano LR, et al.; OC-SELENA Trial. Combined oral contraceptives in women with systemic lupus erythematosus. N Engl J Med. 2005;353(24):2550-2558. doi:10.1056/NEJMoa051135; Seror R, Bowman SJ, Brito-Zeron P, Theander E, Bootsma H, Tzioufas A, et al. EULAR Sjögren’s syndrome disease activity index (ESSDAI): A user guide. RMD Open. 2015;1(1):e000022. doi:10.1136/rmdopen-2014-000022; Seror R, Ravaud P, Mariette X, Bootsma H, Theander E, Hansen A, et al.; EULAR Sjögren’s Task Force. EULAR Sjogren’s syndrome patient reported index (ESSPRI): Development of a consensus patient index for primary Sjogren’s syndrome. Ann Rheum Dis. 2011;70(6):968-972. doi:10.1136/ard.2010.143743; Зурочка АВ, Хайдуков СВ, Кудрявцев ИВ, Чернышев ВА. Проточная цитометрия в биомедицинских исследованиях. Екатеринбург:УрО РАН;2018.; Будкова АИ, Лапин СВ, Серебрякова МК, Кудрявцев ИВ, Тришина ИН, Маслянский АЛ, и др. Субпопуляционный состав В-клеток периферической крови у больных системной красной волчанкой. Медицинская иммунология. 2017;19(2):175-184.; Меснянкина АА, Соловьев СК, Александрова ЕН, Алексанкин АП, Супоницкая ЕВ, Елонаков АВ, и др. Динамика субпопуляции В-лимфоцитов у больных системной красной волчанкой на фоне терапии генно-инженерными биологическими препаратами. Научно-практическая ревматология. 2017;55(3):252-260.; Cornec D, Saraux A, Pers JO, Jousse-Joulin S, Marhadour T, Roguedas-Contios AM, et al. Diagnostic accuracy of blood B-cell subset profiling and autoimmunity markers in Sjögren’s syndrome. Arthritis Res Ther. 2014;16(1):R15. doi:10.1186/ar4442; Barcelos F, Martins C, Papoila A, Geraldes C, Cardigos J, Nunes G, et al. Association between memory B-cells and clinical and immunological features of primary Sjögren’s syndrome and Sicca patients. Rheumatol Int. 2018;38(6):1063-1073. doi:10.1007/s00296-018-4018-0; Ishioka-Takei E, Yoshimoto K, Suzuki K, Nishikawa A, Yasuoka H, Yamaoka K, et al. Increased proportion of a CD38highIgD+ B cell subset in peripheral blood is associated with clinical and immunological features in patients with primary Sjögren’s syndrome. Clin Immunol. 2018;187:85-91. doi:10.1016/j.clim.2017.10.008; Roberts ME, Kaminski D, Jenks SA, Maguire C, Ching K, Burbelo PD, et al. Primary Sjögren’s syndrome is characterized by distinct phenotypic and transcriptional profiles of IgD+ unswitched memory B cells. Arthritis Rheumatol. 2014;66(9):2558-2569. doi:10.1002/art.38734; Odendahl M, Jacobi A, Hansen A, Feist E, Hiepe F, Burmester GR, et al. Disturbed peripheral B lymphocyte homeostasis in systemic lupus erythematosus. J Immunol. 2000;165(10):5970-5979. doi:10.4049/jimmunol.165.10.5970; Hansen A, Odendahl M, Reiter K, Jacobi AM, Feist E, Scholze J, et al. Diminished peripheral blood memory B cells and accumulation of memory B cells in the salivary glands of patients with Sjögren’s syndrome. Arthritis Rheum. 2002;46(8):2160-2171. doi:10.1002/art.10445; Aqrawi LA, Brokstad KA, Jakobsen K, Jonsson R, Skarstein K. Low number of memory B cells in the salivary glands of patients with primary Sjögren’s syndrome. Autoimmunity. 2012;45(7):547-555. doi:10.3109/08916934.2012.712170; Mingueneau M, Boudaoud S, Haskett S, Reynolds TL, Nocturne G, Norton E, et al. Cytometry by time-of-flight immunophenotyping identifies a blood Sjögren’s signature correlating with disease activity and glandular inflammation. J Allergy Clin Immunol. 2016;137(6):1809-1821.e12. doi:10.1016/j.jaci.2016.01.024; Wardowska A, Komorniczak M, Skoniecka A, Bułło-Piontecka B, Lisowska KA, Dębska-Ślizień MA, et al. Alterations in peripheral blood B cells in systemic lupus erythematosus patients with renal insufficiency. Int Immunopharmacol. 2020;83:106451. doi:10.1016/j.intimp.2020.106451; Супоницкая ЕВ, Алексанкин АП, Меснянкина АА, Александрова ЕН, Панафидина ТА, Соловьев СК. Характеристика субпопуляций В-лимфоцитов периферической крови у больных активной системной красной волчанкой. Клиническая лабораторная диагностика. 2017;62(7):418-422.; Enocsson H, Karlsson J, Li HY, Wu Y, Kushner I, Wetterö J, et al. The complex role of C-reactive protein in systemic lupus erythematosus. J Clin Med. 2021;10(24):5837. doi:10.3390/jcm10245837

الاتاحة: https://rsp.mediar-press.net/rsp/article/view/3636
https://doi.org/10.47360/1995-4484-2024-501-512

المؤلفون: S. S. Benevolenskaya, I. V. Kudriavtsev, M. K. Serebriakova, A. A. Rubinstein, E. S. Kuvardin, I. N. Grigor’yeva, D. B. Aliev, D. B. Zammoeva, D. B. Motorin, A. S. Golovkin, O. V. Kalinina, S. V. Lapin, I. Z. Gaydukova, A. L. Maslyanskiy, E. K. Gaydukova, С. С. Беневоленская, И. В. Кудрявцев, М. К. Серебрякова, А. А. Рубинштейн, Е. С. Кувардин, И. Н. Григорьева, Д. Б. Алиев, Д. Б. Заммоева, Д. В. Моторин, А. С. Головкин, О. В. Калинина, С. В. Лапин, И. З. Гайдукова, А. Л. Маслянский, Е. К. Гайдукова

المساهمون: Исследование выполнено при финансовой поддержке Министерства науки и высшего образования Российской Федерации (соглашение № 075-15-2022-301 от 20.04.2022).

المصدر: Rheumatology Science and Practice; Vol 62, No 1 (2024); 90-97 ; Научно-практическая ревматология; Vol 62, No 1 (2024); 90-97 ; 1995-4492 ; 1995-4484

مصطلحات موضوعية: проточная цитометрия, СD8 + T cells, systemic lupus erythematosus, flow cytometry, CD8 + Т-клетки, системная красная волчанка

وصف الملف: application/pdf

Relation: https://rsp.mediar-press.net/rsp/article/view/3517/2352; Насонов ЕЛ (ред.). Ревматология. Российские клинические рекомендации. М.:ГЭОТАР-Медиа;2017.; Насонов ЕЛ. Перспективы анти-В-клеточной терапии в ревматологии. Научно-практическая ревматология. 2018;56(5):539-548. doi:10.14412/1995-4484-2018-539-548; Шадуро ДВ, Белоглазов ВА, Гордиенко АИ. Уровни основных субпопуляций лимфоцитов и их связь с клеточным и гуморальным звеном антиэндотоксинового иммунитета у больных системной красной волчанкой. Медицинская иммунология. 2015;17(4):359-366. doi:10.15789/1563-0625-2015-4-359-366; Blanco P, Pitard V, Viallard JF, Taupin JL, Pellegrin JL, Moreau JF. Increase in activated CD8+ T lymphocytes expressing perforin and granzyme B correlates with disease activity in patients with systemic lupus erythematosus. Arthritis Rheum. 2005;52:201-211. doi:10.1002/art.20745; Couzi L, Merville P, Deminière C, Moreau JF, Combe C, Pellegrin JL, et al. Predominance of CD8+ T lymphocytes among periglomerular infiltrating cells and link to the prognosis of class III and class IV lupus nephritis. Arthritis Rheum. 2007;56(7):2362-2370. doi:10.1002/art.22654; Dolff S, Abdulahad WH, Arends S, van Dijk MC, Limburg PC, Kallenberg CG, et al. Urinary CD8+ T-cell counts discriminate between active and inactive lupus nephritis. Arthritis Res Ther. 2013;15(1):R36. doi:10.1186/ar4189; Klocke J, Kopetschke K, Grießbach AS, Langhans V, Humrich JY, Biesen R, et al. Mapping urinary chemokines in human lupus nephritis: Potentially redundant pathways recruit CD4+ and CD8+ T cells and macrophages. Eur J Immunol. 2017;47(1):180-192. doi:10.1002/eji.201646387; Yuan S, Zeng Y, Li J, Wang C, Li W, He Z, et al. Phenotypical changes and clinical significance of CD4+/CD8+ T cells in SLE. Lupus Sci Med. 2022;9(1):e000660. doi:10.1136/lupus-2022-000660; St Paul M, Ohashi PS. The roles of CD8+ T cell subsets in antitumor immunity. Trends Cell Biol. 2020;30(9):695-704. doi:10.1016/j.tcb.2020.06.003; Fousteri G, Kuka M. The elusive identity of CXCR5+ CD8 T cells in viral infection and autoimmunity: Cytotoxic, regulatory, or helper cells? Mol Immunol. 2020;119:101-105. doi:10.1016/j.molimm.2020.01.007; 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. Arthritis Rheumatol. 2019;71(9):1400-1412. doi:10.1002/art.40930; Кудрявцев ИВ, Борисов АГ, Кробинец ИИ, Савченко АА, Серебрякова МК, Тотолян АА. Хемокиновые рецепторы на Т-хелперах различного уровня дифференцировки: основные субпопуляции. Медицинская иммунология. 2016;18(3):239-250. doi:10.15789/1563-0625-2016-3-239-250; Loyal L, Warth S, Jürchott K, Mölder F, Nikolaou C, Babel N, et al. SLAMF7 and IL-6R define distinct cytotoxic versus helper memory CD8+ T cells. Nat Commun. 2020;11(1):6357. doi:10.1038/s41467-020-19002-6; Kudryavtsev IV, Arsentieva NA, Korobova ZR, Isakov DV, Rubinstein AA, Batsunov OK, et al. Heterogenous CD8+ T cell maturation and ‘polarization’ in acute and convalescent COVID19 patients. Viruses. 2022;14(9):1906. doi:10.3390/v14091906; Chen J, Ding L, Meng W, Yang J, Yan C, Xie J, et al. Vincristinecyclophosphamide combination therapy positively affects T-cell subset distribution in systemic lupus erythematosus patients. Med Sci Monit. 2015;21:505-510. doi:10.12659/MSM.893271; Chen PM, Tsokos GC. The role of CD8+ T-cell systemic lupus erythematosus pathogenesis: An update. Curr Opin Rheumatol. 2021;33(6):586-591. doi:10.1097/BOR.0000000000000815; Postal M, Appenzeller S. The role of tumor necrosis factor-alpha (TNF-α) in the pathogenesis of systemic lupus erythematosus. Cytokine. 2011;56(3):537-543. doi:10.1016/j.cyto.2011.08.026; Jacob CO, McDevitt HO. Tumor necrosis factor-alpha in murine autoimmune ‘lupus’ nephritis. Nature. 1988;331:356-358. doi:10.1038/331356a0; López P, Gutiérrez C, Suárez A. IL-10 and TNFα genotypes in SLE. J Biomed Biotechnol. 2010;2010:838390. doi:10.1155/2010/838390; Bridgewood C, Wittmann M, Macleod T, Watad A, Newton D, Bhan K, et al. T helper 2 IL-4/IL-13 dual blockade with dupilumab is linked to some emergent T helper 17-type diseases, including seronegative arthritis and enthesitis/enthesopathy, but not to humoral autoimmune diseases. J Invest Dermatol. 2022;142(10):2660-2667. doi:10.1016/j.jid.2022.03.013; https://rsp.mediar-press.net/rsp/article/view/3517

الاتاحة: https://rsp.mediar-press.net/rsp/article/view/3517
https://doi.org/10.47360/1995-4484-2024-90-97

المؤلفون: E. S. Kuvardin, I. V. Kholopova, E. A. Belyakova, I. N. Grigoryeva, A. V. Masing, O. Yu. Tkachenko, I. A. Bekhtereva, A. L. Maslyansky, Yu. A. Krivolapov, S. V. Lapin, Е. С. Кувардин, И. В. Холопова, Е. А. Белякова, И. Н. Григорьева, А. В. Мазинг, О. Ю. Ткаченко, И. А. Бехтерева, А. Л. Маслянский, Ю. А. Криволапов, С. В. Лапин

المصدر: Modern Rheumatology Journal; Том 17, № 1 (2023); 24–30 ; Современная ревматология; Том 17, № 1 (2023); 24–30 ; 2310-158X ; 1996-7012

مصطلحات موضوعية: плазматические клетки, immunoglobulin free light chains, saliva, plasma cells, свободные легкие цепи иммуноглобулинов, слюна

وصف الملف: application/pdf

Relation: https://mrj.ima-press.net/mrj/article/view/1384/1322; Shiboski CH, Shiboski SC, Seror R, et al. 2016 American College of Rheumatology/European League Against Rheumatism Classification Criteria for Primary Sjцgren's Syndrome: A Consensus and Data-Driven Methodology Involving Three International Patient Cohorts. Arthritis Rheumatol. 2017 Jan;69(1): 35-45. doi:10.1002/art.39859. Epub 2016 Oct 26.; Qin B, Wang J, Yang Z, et al. Epidemiology of primary Sjцgren's syndrome: a systematic review and meta-analysis. Ann Rheum Dis. 2015 Nov;74(11):1983-9. doi:10.1136/annrheumdis-2014-2053. Epub 2014 Jun 17.; Caporali R, Bonacci E, Epis O, et al. Safety and usefulness of minor salivary gland biopsy: retrospective analysis of 502 procedures performed at a single center. Arthritis Rheum. 2008 May 15;59(5):714-20. doi:10.1002/art.23579.; Thorlacius GE, Hultin-Rosenberg L, Sandling JK, et al. Genetic and clinical basis for two distinct subtypes of primary Sjоgren's syndrome. Rheumatology (Oxford). 2021 Feb 1; 60(2):837-48. doi:10.1093/rheumatology/keaa367.; Carubbi F, Alunno A, Cipriani P, et al. Different operators and histologic techniques in the assessment of germinal center-like structures in primary Sjцgren's syndrome minor salivary glands. PLoS One. 2019 Jan 25;14(1):e0211142. doi:10.1371/journal.pone.0211142. eCollection 2019.; Shoenfeld Y, Meroni PL, Gershwin ME. Autoantibodies. Waltham: Elsevier; 2014. P. 233-8.; Brito-Zerуn P, Acar-Denizli N, Zeher M, et al. How does primary Sjögren syndrome present in biopsy-proven patients without circulating rola autoantibodies? Characteristics at diagnosis of 2073 patients from the Sjögren big data project. https://acrabstracts.org/abstract/sjogren-big-data-project-influence-ofgeolocation-on-the-phenotypic-expressionat-diagnosis-in-8310-patients-north-tosouth-gradient/; Aqrawi LA, Galtung HK, Guerreiro EM, et al. Proteomic and histopathological characterisation of sicca subjects and primary Sjögren's syndrome patients reveals promising tear, saliva and extracellular vesicle disease biomarkers. Arthritis Res Ther. 2019 Jul 31; 21(1):181. doi:10.1186/s13075-019-1961-4.; Christodoulou MI, Kapsogeorgou EK, Moutsopoulos HM. Characteristics of the minor salivary gland infiltrates in Sjögren's syndrome. J Autoimmun. 2010 Jun;34(4):400-7. doi:10.1016/j.jaut.2009.10.004. Epub 2009 Nov 3.; Nocturne G, Mariette X. B cells in the pathogenesis of primary Sjögren syndrome. Nat Rev Rheumatol. 2018 Mar;14(3):133-45. doi:10.1038/nrrheum.2018.1. Epub 2018 Feb 8.; Sandhya P, Christudoss P, Kabeerdoss J, et al. Diagnostic accuracy of salivary and serum-free light chain assays in primary Sjögren's syndrome: a pilot study. Int J Rheum Dis. 2017 Jun;20(6):760-766. doi:10.1111/1756-185X.12965. Epub 2016 Dec 30.; Verstappen GM, Moerman RV, van Nimwegen JF, et al. Serum immunoglobulin free light chains are sensitive biomarkers for monitoring disease activity and treatment response in primary Sjögren's syndrome. Rheumatology (Oxford). 2018 Oct 1;57(10):1812-21. doi:10.1093/rheumatology/key180.; Navazesh M, Kumar SK. Measuring salivary flow: challenges and opportunities. J Am Dent Assoc. 2008 May;139 Suppl:35S-40S. doi:10.14219/jada.archive.2008.; Тотолян АА. Современные подходы к диагностике иммунопатологических состояний. Медицинская иммунология. 1999;1(1-2):75-108.; Teppo H, Revonta M. A follow-up study of minimally invasive lip biopsy in the diagnosis of Sjögren's syndrome. Clin Rheumatol. 2007 Jul;26(7):1099-103. doi:10.1007/s10067-006-0457-1. Epub 2006 Nov 25.; Katsiougiannis S, Wong DTW. The Proteomics of Saliva in Sjögren's Syndrome. Rheum Dis Clin North Am. 2016;42(3):449-56. doi:10.1016/j.rdc.2016.03.004. Epub 2016 Jun 21.; Szyszko EA, Brokstad KA, Oijordsbakken G, et al. Salivary glands of primary Sjögren's syndrome patients express factors vital for plasma cell survival. Arthritis Res Ther. 2011 Jan 7;13(1):R2. doi:10.1186/ar3220.; Mingueneau M, Boudaoud S, Haskett S, et al. Cytometry by time-of-flight immunophenotyping identifies a blood Sjögren's signature correlating with disease activity and glandular inflammation. J Allergy Clin Immunol. 2016 Jun;137(6):1809-21.e12. doi:10.1016/j.jaci.2016.01.024. Epub 2016 Apr 1.; Будкова АИ, Лапин СВ, Серебрякова МК и др. Субпопуляционный состав В-клеток периферической крови у больных системной красной волчанкой. Медицинская иммунология. 2017;19(2):175-84.; Hamza N, Bootsma H, Yuvaraj S, et al. Persistence of immunoglobulin-producing cells in parotid salivary glands of patients with primary Sjögren's syndrome after B cell depletion therapy. Ann Rheum Dis. 2012 Nov;71(11): 1881-7. doi:10.1136/annrheumdis-2011-201189. Epub 2012 May 21.; Takeshita M, Suzuki K, Kaneda Y, et al. Antigen-driven selection of antibodies against SSA, SSB and the centromere 'complex', including a novel antigen, MIS12 complex, in human salivary glands. Ann Rheum Dis. 2020 Jan;79(1):150-8. doi:10.1136/annrheumdis-2019-215862. Epub 2019 Oct 14.; Bookman AA, Shen H, Cook RJ, et al. Whole stimulated salivary flow: correlation with the pathology of inflammation and damage in minor salivary gland biopsy specimens from patients with primary Sjögren's syndrome but not patients with sicca. Arthritis Rheum. 2011 Jul;63(7):2014-20. doi:10.1002/art.30295.; Tarn JR, Howard-Tripp N, Lendrem DW, et al. Symptom-based stratification of patients with primary Sjögren's syndrome: multi-dimensional characterisation of international observational cohorts and reanalyses of randomised clinical trials. Lancet Rheumatol. 2019 Sep 25;1(2):e85-94. doi:10.1016/S2665-9913(19)30042-6.; Sandhya P, Kabeerdoss J, Christudoss P, et al. Salivary free light chains and salivary immunoglobulins as potential non-invasive biomarkers in primary Sjögren's syndrome. Int J Rheum Dis. 2022;25(1):61-9. doi:10.1111/1756-185X.14242. Epub 2021 Nov 17.; Fox PC, Datiles M, Atkinson JC, et al. Prednisone and piroxicam for treatment of primary Sjögren's syndrome. Clin Exp Rheumatol. 1993 Mar-Apr;11(2):149-56.; https://mrj.ima-press.net/mrj/article/view/1384

الاتاحة: https://mrj.ima-press.net/mrj/article/view/1384
https://doi.org/10.14412/1996-7012-2023-1-24-30

المؤلفون: P. V. Berezhansky, N. S. Tataurschikova, T. G. Fedoskova, O. I. Letyaeva, A. S. Rusanova, I. N. Grigorieva, A. A. Kameleva, A. E. Dobrenkaya, A. I. Vasilkova, П. В. Бережанский, Н. С. Татаурщикова, Т. Г. Федоскова, О. И. Летяева, А. С. Русанова, И. Н. Григорьева, А. А. Камелева, А. Е. Добренькая, А. И. Василькова

المصدر: Medical Immunology (Russia); Том 24, № 3 (2022); 519-526 ; Медицинская иммунология; Том 24, № 3 (2022); 519-526 ; 2313-741X ; 1563-0625

مصطلحات موضوعية: обострение астмы, adhesion molecules, virus, allergic inflammation, asthma exacerbation, молекулы адгезии, вирус, аллергическое воспаление

وصف الملف: application/pdf

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الاتاحة: https://www.mimmun.ru/mimmun/article/view/2478
https://doi.org/10.15789/1563-0625-ROL-2478

المؤلفون: E. S. Kuvardin, I. N. Grigor’yeva, I. A. Bekhtereva, A. L. Maslyansky, Yu. A. Krivolapov, E. A. Belyakova, Е. С. Кувардин, И. Н. Григорьева, И. А. Бехтерева, А. Л. Маслянский, Ю. А. Криволапов, Е. А. Белякова

المصدر: Rheumatology Science and Practice; Vol 59, No 4 (2021); 434–441 ; Научно-практическая ревматология; Vol 59, No 4 (2021); 434–441 ; 1995-4492 ; 1995-4484

مصطلحات موضوعية: плазматические клетки, biopsy, immunohistochemistry, small salivary gland, T cells, B cells, macrophages, follicular dendritic cells, plasmacytes, биопсия, иммуногистохимическое исследование, малая слюнная железа, Т-клетки, В-клетки, макрофаги, фолликулярные дендритные клетки

وصف الملف: application/pdf

Relation: https://rsp.mediar-press.net/rsp/article/view/3061/2113; Насонов ЕЛ (ред.). Ревматология. Российские клинические рекомендации. М.:ГЭОТАР-Медиа;2017:464.; Qin B, Wang J, Yang Z, Yang M, Ma N, Huang F, et al. Epidemiology of primary Sjögren’s syndrome: A systematic review and meta-analysis. Ann Rheum Dis. 2015;74:1983-1989. doi:10.1136/annrheumdis-2014-205375; Shiboski CH, Shiboski SC, Seror R, Criswell LA, Labetoulle M, Lietman TM, et al. 2016 American College of Rheumatology/ European League Against Rheumatism classification criteria for primary Sjögren’s syndrome: A consensus and data-driven methodology involving three international patient cohorts. Arthritis Rheumatol. 2017;69:35-45. doi:10.1002/art.39859; Guellec D, Cornec D, Jousse-Joulin S, Marhadour T, Marcorelles P, Pers JO, et al. Diagnostic value of labial minor salivary gland biopsy for Sjögren’s syndrome: A systematic review. Autoimmun Rev. 2013;12:416-420. doi:10.1016/j.autrev.2012.08.001; Bodeutsch C, de Wilde PC, Kater L, van Houwelingen JC, van den Hoogen FH, Kruize AA, et al. Quantitative immunohistologic criteria are superior to the lymphocytic focus score criterion for the diagnosis of Sjögren’s syndrome. Arthritis Rheum. 1992;35:1075-1087. doi:10.1002/art.1780350913; van Woerkom JM, Kruize AA, Barendregt PJ, Kater L, Hené R, Bootsma H, et al. Clinical significance of quantitative immunohistology in labial salivary glands for diagnosing Sjogren’s syndrome. Rheumatology (Oxford). 2006;45:470-477. doi:10.1093/rheumatology/kei191; Fisher BA, Jonsson R, Daniels T, Bombardieri M, Brown RM, Morgan P, et al. Standardisation of labial salivary gland histopathology in clinical trials in primary Sjogren’s syndrome. Ann Rheum Dis. 2017;76:1161-1168. doi:10.1136/annrheumdis-2016-210448; Navazesh M, Kumar SKS. Measuring salivary flow. Dent Assist J. 2008;139:35S-40S. doi:10.14219/jada.archive.2008.0353; Teppo H, Revonta M. A follow-up study of minimally invasive lip biopsy in the diagnosis of Sjögren’s syndrome. Clin Rheumatol. 2007;26:1099-1103. doi:10.1007/s10067-006-0457-1; Quartuccio L, Baldini C, Bartoloni E, Priori R, Carubbi F, Corazza L, et al. Anti-SSA/SSB-negative Sjögren’s syndrome shows a lower prevalence of lymphoproliferative manifestations, and a lower risk of lymphoma evolution. Autoimmun Rev. 2015;14:1019-1022. doi:10.1016/j.autrev.2015.07.002; Christodoulou MI, Kapsogeorgou EK, Moutsopoulos HM. Characteristics of the minor salivary gland infiltrates in Sjögren’s syndrome. J Autoimmun. 2010;34:400–407. doi:10.1016/j.jaut.2009.10.004; Jonsson MV, Skarstein K. Follicular dendritic cells confirm lymphoid organization in the minor salivary glands of primary Sjögren’s syndrome. J Oral Pathol Med. 2008;37:515-521. doi:10.1111/j.1600-0714.2008.00674.x; Braun M, Melchers I, Peter HH, Illges H. Human B and T lymphocytes have similar amounts of CD21 mRNA, but differ in surface expression of the CD21 glycoprotein. Int Immunol. 1998;10(8):1197-1202.; Daridon C, Pers JO, Devauchelle V, Martins-Carvalho C, Hutin P, Pennec YL, et al. Identification of transitional type II B cells in the salivary glands of patients with Sjögren’s syndrome. Arthritis Rheum. 2006;54:2280-2288. doi:10.1002/art.21936; Le Pottier L, Devauchelle V, Fautrel A, Daridon C, Saraux A, Youinou P, et al. Ectopic germinal centers are rare in Sjogren’s syndrome salivary glands and do not exclude autoreactive B cells. J Immunol. 2009;182:3540-3547. doi:10.4049/jimmunol.0803588; Ushio A, Arakaki R, Yamada A, Saito M, Tsunematsu T, Kudo Y, et al. Crucial roles of macrophages in the pathogenesis of autoimmune disease. World J Immunol. 2017;7(1):1-8. doi:10.5411/wji.v7.i1.1; Ushio A, Arakaki R, Otsuka K, Yamada A, Tsunematsu T, Kudo Y, et al. CCL22-producing resident macrophages enhance T cell response in Sjögren’s syndrome. Front Immunol. 2018;9:2594. doi:10.3389/fimmu.2018.02594; https://rsp.mediar-press.net/rsp/article/view/3061

الاتاحة: https://rsp.mediar-press.net/rsp/article/view/3061
https://doi.org/10.47360/1995-4484-2021-434-441