يعرض 1 - 10 نتائج من 594 نتيجة بحث عن '"Interféron-α"', وقت الاستعلام: 0.91s تنقيح النتائج
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    دورية أكاديمية

    المساهمون: Harrer, Dc, Lüke, F, Pukrop, T, Ghibelli, L, Gerner, C, Reichle, A, Heudobler, D

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/38273846; info:eu-repo/semantics/altIdentifier/wos/WOS:001149028800001; volume:13; numberofpages:16; journal:FRONTIERS IN ONCOLOGY; https://hdl.handle.net/2108/353508Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85182976686

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    دورية أكاديمية
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    دورية أكاديمية
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    دورية أكاديمية

    العلاقة: García-Ortega, M.B.; Aparicio, E.; Griñán-Lisón, C.; Jiménez, G.; López-Ruiz, E.; Palacios, J.L.; Ruiz-Alcalá, G.; Alba, C.; Martínez, A.; Boulaiz, H.; et al. Interferon-Alpha Decreases Cancer Stem Cell Properties and Modulates Exosomes in Malignant Melanoma. Cancers 2023, 15, 3666. [https:// doi.org/10.3390/cancers15143666]; https://hdl.handle.net/10481/84587Test

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    دورية أكاديمية
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    دورية أكاديمية

    المساهمون: The article was prepared within the framework of the basic scientific topic FURS-2022-003 №122040400024-07., Статья подготовлена в рамках фундаментальной темы FURS-2022-003 №122040400024-07.

    المصدر: Modern Rheumatology Journal; Том 17, № 6 (2023); 14-21 ; Современная ревматология; Том 17, № 6 (2023); 14-21 ; 2310-158X ; 1996-7012

    وصف الملف: application/pdf

    العلاقة: https://mrj.ima-press.net/mrj/article/view/1497/1410Test; https://mrj.ima-press.net/mrj/article/view/1497/1412Test; Насонов ЕЛ, Соловьев СК, Аршинов АВ. Системная красная волчанка: история и современность. Научно-практическая ревматология. 2022;60(4):397-412.; Crow MK, Olferiev M, Kirou KA. Type I interferons in autoimmune disease. Annu Rev Pathol. 2019 Jan 24:14:369-393. doi:10.1146/annurev-pathol-020117-043952. Epub 2018 Oct 17.; Насонов ЕЛ, Авдеева АС. Иммуновоспалительные ревматические заболевания, связанные с интерфероном типа I: новые данные. Научно-практическая ревматология. 2019;57(4):452-461.; Rönnblom L, Leonard D. Interferon pathway in SLE: One key to unlocking the mystery of the disease. Lupus Sci Med. 2019 Aug 13;6(1):e000270. doi:10.1136/lupus-2018-000270. eCollection 2019.; Reshetnyak T, Nurbaeva K, Ptashnik I, et al. Markers of NETosis in Patients with Systemic Lupus Erythematosus and Antiphospholipid Syndrome. Int J Mol Sci. 2023; 24(11):9210. doi:10.3390/ijms24119210.; Sarkar MK, Hile GA, Tsoi LC, et al. Photosensitivity and type I IFN responses in cutaneous lupus are driven by epidermal-derived interferon kappa. Ann Rheum Dis. 2018 Nov; 77(11):1653-1664. doi:10.1136/annrheumdis-2018-213197. Epub 2018 Jul 18.; Braunstein I, Klein R, Okawa J, Werth VP. The interferon-regulated gene signature is elevated in subacute cutaneous lupus erythematosus and discoid lupus erythematosus and correlates with the cutaneous lupus area and severity index score. Br J Dermatol. 2012 May; 166(5):971-5. doi:10.1111/j.1365-2133.2012.10825.x.; Nzeusseu Toukap A, Galant C, Theate I, et al. Identification of distinct gene expression profiles in the synovium of patients with systemic lupus erythematosus. Arthritis Rheum. 2007 May;56(5):1579-88. doi:10.1002/art.22578.; Castellano G, Cafiero C, Divella C, et al. Local synthesis of interferon-alpha in lupus nephritis is associated with type I interferons signature and LMP7 induction in renal tubular epithelial cells. Arthritis Res Ther. 2015 Mar 22;17(1):72. doi:10.1186/s13075-015-0588-3.; Shiozawa S, Kuroki Y, Kim M, et al. Interferonalpha in lupus psychosis. Arthritis Rheum. 1992 Apr;35(4):417-22. doi:10.1002/art.1780350410.; Schneider WM, Chevillotte MD, Rice CM. Interferon-stimulated genes: a complex web of host defenses. Annu Rev Immunol. 2014:32: 513-45. doi:10.1146/annurev-immunol032713-120231. Epub 2014 Feb 6.; Ivashkiv LB, Donlin LT. Regulation of type I interferon responses. Nat Rev Immunol. 2014 Jan;14(1):36-49. doi:10.1038/nri3581.; Paredes JL, Niewold TB. Type I interferon antagonists in clinical development for lupus. Expert Opin Investig Drugs. 2020 Sep;29(9): 1025-1041. doi:10.1080/13543784.2020. 1797677. Epub 2020 Sep 1.; Chaichian Y, Strand V. Interferon-directed therapies for the treatment of systemic lupus erythematosus: a critical update. Clin Rheumatol. 2021 Aug;40(8):3027-3037. doi:10.1007/s10067-020-05526-1. Epub 2021 Jan 7.; Goulden B, Isenberg D. Anti-IFN R MAbs for the treatment of systemic lupus erythematosus. Expert Opin Biol Ther. 2021 Apr;21(4):519-528. doi:10.1080/14712598.2021.1841164. Epub 2020 Oct 30.; Peng L, Oganesyan V, Wu H, et al. Molecular basis for antagonistic activity of anifrolumab, an anti-interferon-α receptor 1 antibody. MAbs. 2015;7(2):428-39. doi:10.1080/19420862.2015.1007810.; Riggs JM, Hanna RN, Rajan B, et al. Characterisation of anifrolumab, a fully human anti-interferon receptor antagonist antibody for the treatment of systemic lupus erythematosus. Lupus Sci Med. 2018 Apr 5;5(1): e000261. doi:10.1136/lupus-2018-000261. eCollection 2018.; Инструкция по медицинскому применению лекарственного препарата САФНЕЛО®, 300 мг (концентрат для приготовления раствора для инфузий). Регистрационное удостоверение ЛП-№(001857)-(РГ-RU) от 27.02.2023 г.; Petri M, Orbai AM, Alarcуn GS, et al. Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus. Arthritis Rheum. 2012 Aug;64(8): 2677-86. doi:10.1002/art.34473.; Gladman DD, Ibanez D, Urowitz MB. Systemic lupus erythematosus disease activity index 2000. J Rheumatol. 2002 Feb;29(2): 288-91.; Albrecht J, Taylor L, Berlin JA, et al. The CLASI (Cutaneous Lupus Erythematosus Disease Area and Severity Index): an outcome instrument for cutaneous lupus erythematosus. J Invest Dermatol. 2005 Nov;125(5):889-94. doi:10.1111/j.0022-202X.2005.23889.x.; Klein R, Moghadam-Kia S, LoMonico J, et al. Development of the CLASI as a tool to measure disease severity and responsiveness to therapy in cutaneous lupus erythematosus. Arch Dermatol. 2011 Feb;147(2):203-8. doi:10.1001/archdermatol.2010.435; Gladman D, Ginzler E, Goldsmith C, et al. The development and initial validation of the Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index for systemic lupus erythematosus. Arthritis Rheum. 1996 Mar;39(3): 363-9. doi:10.1002/art.1780390303.; McElhone K, Abbott J, Shelmerdine J, et al. Development and validation of a disease-specific health-related quality of life measure, the LupusQol, for adults with systemic lupus erythematosus. Arthritis Rheum. 2007 Aug 15;57(6):972-9. doi:10.1002/art.22881; Yellen S. Measuring fatigue and other anemia-related symptoms with the Functional Assessment of Cancer Therapy (FACIT) measurement system. J Pain Symptom Manage. 1997 Feb;13(2):63-74. doi:10.1016/s0885-3924(96)00274-6.; Pilgaard T, Hagelund L, Stallknecht SE, et al. Severity of fatigue in people with rheumatoid arthritis, psoriatic arthritis and spondyloarthritis – Results of a cross-sectional study. PLoS One. 2019 Jun 28;14(6):e0218831. doi:10.1371/journal.pone.0218831.; Miyakis S, Lockshin MD, Atsumi T, et al. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thromb Haemost. 2006 Feb;4(2):295-306. doi:10.1111/j.1538-7836.2006.01753.x.; Насонов ЕЛ, редактор. Российские клинические рекомендации. Ревматология. Москва: ГЭОТАР-Медиа; 2017. 464 с.; Kalunian KC, Furie R, Morand EF, et al. A Randomized, Placebo-Controlled Phase III Extension Trial of the Long-Term Safety and Tolerability of Anifrolumab in Active Systemic Lupus Erythematosus. Arthritis Rheumatol. 2023 Feb;75(2):253-265. doi:10.1002/art.42392. Epub 2022 Nov 11.; Morand EF, Trasieva T, Berglind A, et al. Lupus Low Disease Activity State (LLDAS) attainment discriminates responders in a systemic lupus erythematosus trial: post-hoc analysis of the Phase IIb MUSE trial of anifrolumab. Ann Rheum Dis. 2018 May;77(5):706-713. doi:10.1136/annrheumdis-2017-212504. Epub 2018 Feb 2.; Асеева ЕА, Воробьева ЛД, Соловьев СК и др. Психометрические свойства русскоязычной версии специфического опросника LupusQol для оценки качества жизни, связанного со здоровьем, у пациентов с системной красной волчанкой. Научнопрактическая ревматология. 2018;56(2): 164-172.; Furie RA, Morand EF, Bruce IN, et al. Type I interferon inhibitor anifrolumab in active systemic lupus erythematosus (TULIP-1): a randomised, controlled, phase 3 trial. Lancet Rheumatol. 2019;(1):e208-19.; Morand EF, Furie R, Tanaka Y, et al; TULIP-2 Trial Investigators. Trial of anifrolumab in active systemic lupus erythematosus. N Engl J Med. 2020 Jan 16;382(3):211-221. doi:10.1056/NEJMoa1912196. Epub 2019 Dec 18.; Bruce IN, Golam S, Steenkamp J, et al. Indirect treatment comparison of anifrolumab efficacy versus belimumab in adults with systemic lupus erythematosus. J Comp Eff Res. 2022 Jul;11(10):765-777. doi:10.2217/cer-2022-0040. Epub 2022 May 12.; Neupane B, Shukla P, Slim M, et al. Belimumab versus anifrolumab in adults with systemic lupus erythematosus: an indirect comparison of clinical response at 52 weeks. Lupus Sci Med. 2023 May;10(1):e000907. doi:10.1136/lupus-2023-000907.; https://mrj.ima-press.net/mrj/article/view/1497Test

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    دورية أكاديمية

    المساهمون: The study was performed without external funding

    المصدر: Biological Products. Prevention, Diagnosis, Treatment; Том 23, № 3 (2023); 290-299 ; БИОпрепараты. Профилактика, диагностика, лечение; Том 23, № 3 (2023); 290-299 ; 2619-1156 ; 2221-996X

    وصف الملف: application/pdf

    العلاقة: https://www.biopreparations.ru/jour/article/view/453/742Test; https://www.biopreparations.ru/jour/article/downloadSuppFile/453/507Test; https://www.biopreparations.ru/jour/article/downloadSuppFile/453/750Test; Cucinotta D, Vanelli M. WHO declares COVID-19 a pandemic. Acta Biomed. 2020;91(1):157–60. https://doi.org/10.23750/abm.v91i1.9397Test; Seyedpour S, Khodaei B, Loghman AH, Seyedpour N, Kisomi MF, Balibegloo M, et al. Targeted therapy strategies against SARS‐CoV‐2, cell entry mechanisms: A systematic review of in vitro and in vivo studies. J Cell Physiol. 2020;236(4):2364–92. https://doi.org/10.1002/jcp.30032Test; Болевич CБ, Болевич СС. Комплексный механизм развития СOVID-19. Сеченовский вестник. 2020;11(2):50–61 https://doi.org/10.47093/2218-7332.2020.11.2.50-61Test; Andreev-Andrievskiy AA, Zinovkin RA, Mashkin MA, Frolova OY, Kazaishvili YG, Scherbakova VS, et al. Gene expression pattern of Peyer’s patch lymphocytes exposed to kagocel suggests pattern-recognition receptors mediate its action. Front Pharmacol. 2021;12:679511. https://doi.org/10.3389/fphar.2021.679511Test; Gu W, Gan H, Ma Y, Xu L, Cheng J, Li B, et al. The molecular mechanism of SARS-CoV-2 evading host antiviral innate immunity. Virol J. 2022;19(1):49. https://doi.org/10.1186/s12985-022-01783-5Test; Костинов МП, Маркелова ЕВ, Свитич ОА, Полищук ВБ. Иммунные механизмы SARS-СoV-2 и потенциальные препараты для профилактики и лечения COVID-19. Пульмонология. 2020;30(5):700–8. https://doi.org/10.18093/0869-0189-2020-30-5-700-708Test; Barnard DL, Day CW, Bailey K, Heiner M, Montgomery R, Lauridsen L, et al. Evaluation of immunomodulators, interferons and known in vitro SARS-CoV inhibitors for inhibition of SARS-CoV replication in BALB/c mice. Antivir Chem Chemother. 2006;17(5):275–84. https://doi.org/10.1177/095632020601700505Test; Day CW, Baric R, Cai SX, Frieman M, Kumaki Y, Morrey JD, et al. A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo. Virology. 2009;395(2):210–22. https://doi.org/10.1016/j.virol.2009.09.023Test; Overton ET, Goepfert PA, Cunningham P, Carter WA, Horvath J, Young D, Strayer DR. Intranasal seasonal influenza vaccine and a TLR-3 agonist, rintatolimod, induced cross-reactive IgA antibody formation against avian H5N1 and H7N9 influenza HA in humans. Vaccine. 2014;32(42):5490–5. https://doi.org/10.1016/j.vaccine.2014.07.078Test; Kozlowski A, Charles SA, Harris JM. Development of pegylated interferons for the treatment of chronic hepatitis C. BioDrugs. 2001;15(7):419–29. https://doi.org/10.2165/00063030-200115070-00001Test; Nicodemus CF, Berek JS. TLR3 agonists as immunotherapeutic agents. Immunotherapy. 2010;2(2):137–40. https://doi.org/10.2217/imt.10.8Test; Mustafa DAM, Saida L, Latifi D, Wismans LV, de Koning W, Zeneyedpour L. Rintatolimod induces antiviral activities in human pancreatic cancer cells: opening for an Anti-COVID-19 opportunity in cancer patients. Cancers (Basel). 2021;13(2):2896. https://doi.org/10.3390/cancers13122896Test; Ершов ФИ, Киселев ОИ. Интерфероны и их индукторы (от молекул до лекарств). М.: ГЭОТАР-Медиа; 2005.; Kozlovskaya L, Piniaeva A, Ignatyev G, Selivanov A, Shishova A, Kovpak A, et al. Isolation and phylogenetic analysis of SARS-CoV-2 variants collected in Russia during the COVID-19 outbreak. Int J Infect Dis. 2020;99:40–6. https://doi.org/10.1016/j.ijid.2020.07.024Test; Ianevski A, Yao R, Zusinaite E, Lello LS, Wang S, Jo E, et al. Synergistic interferon-alpha-based combinations for treatment of SARS-CoV-2 and other viral infections. Viruses. 2021;13(12):2489. https://doi.org/10.3390/v13122489Test; Sallard E, Lescure FX, Yazdanpanah Y, Mentre F, Peiffer-Smadja N. Type 1 interferons as a potential treatment against COVID-19. Antiviral Res. 2020;178:104791. https://doi.org/10.1016/j.antiviral.2020.104791Test; Ribero MS, Jouvenet N, Dreux M, Nisole S. Interplay between SARS-CoV-2 and the type I interferon response. PLoS Pathog. 2020;16(7):e1008737. https://doi.org/10.1371/journal.ppat.1008737Test; Todorović-Raković N, Whitfield JR. Between immunomodulation and immunotolerance: The role of IFNγ in SARS-CoV-2 disease. Cytokine. 2021;146:155637. https://doi.org/10.1016/j.cyto.2021.155637Test; Karber G. Beitragzurkollecktiven behandlungpharmakologischer reihenversuche. Arch Exptl Pathol Pharmakol. 1931;162:480–3.; Villinger F, Brar SS, Mayne A, Chikkala N, Ansari AA. Comparative sequence analysis of cytokine genes from human and nonhuman primates. J Immunol. 1995;155:3946–54. https://doi.org/10.4049/jimmunol.155.8.3946Test; Felger JS, Alagbe O, Hu F, Mook D, Freeman AA, Sanchez MM, et al. Effects of interferon-alpha on rhesus monkeys: a non-human primate model of cytokine-induced depression. Biol Psychiatry. 2007;62(11):1324–33. https://doi.org/10.1016%2Fj.biopsych.2007.05.026Test; Willette AA, Lubach GR, Coe CL. Environmental context differentially affects behavioral, leukocyte, cortisol, and interleukin-6 responses to low doses of endotoxin in the rhesus monkey. Brain Behav Immun. 2007;21(6):807–15. https://doi.org/10.1016/j.bbi.2007.01.007Test; https://www.biopreparations.ru/jour/article/view/453Test

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