Название | Клеточные и молекулярные механизмы патогенеза иммуновоспалительных ревматических заболеваний |
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Автор произведения | Марат Зиявдинович Саидов |
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Год выпуска | 2023 |
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79. Khandpur R., Carmona-Rivera C., Vivekanandan-Giri A., Gizinski A., Yalavarthi S., Knight J. S. NETs are a source of citrullinated autoantigens and stimulate inflammatory responses in rheumatoid arthritis. Sci. Transl. Med., 2013; 5(178):178ra40. doi: 10.1126/scitranslmed.3005580.
80. Kiselyov A. et al. VEGF/VEGFR signaling as a target for inhibiting angiogenesis. Expert Opin. Investig. Drugs, 2007, Vol. 16, pp. 83–107.
81. Klemperer P. The concept of collagen diseases. The American Journal of Pathology, 1950; Vol. XXVI, no. 4, pp. 505–519.
82. Knecht, H., Saremaslani, P., Hedinger, C. Immunohistological findings in Hashimoto’s thyroiditis, focal lymphocytic thyroiditis and thyroiditis de Quervain. Virchows Arch., 1981; A 393, pp. 215–231. https://sci-hub.do/10.1007/bf00431078.
83. Knight J. S., Carmona-Rivera C., Kaplan M. J. Proteins derived from neutrophil extracellular traps may serve as self-antigens and mediate organ damage in autoimmune diseases. Front Immunol., 2012, Vol. 3, pp.380. doi: 10.3389/fimmu.2012.00380. eCollection 2012.
84. Kobayashi K., Kaneda K., Kasama T. Immunopathogenesis of Delayed-Type Hypersensitivity. Microscopy Research and Technique, 2001, Vol. 53, no.4, pp. 241–245. doi: 10.1002/jemt.1090.
85. Koch A. E. Angiogenesis: implications for rheumatoid arthritis. Arthritis Rheum., 1998, Vol. 41, no.6, pp.951–962. doi:10.1002/1529–0131(199806)41:6<951::AID-ART2>3.0.CO;2-D.
86. Koelink P. J., Overbeek. S. A., Braber S., Henricks P. A., Roda M.A….Kraneveld A. D.. Collagen degradation and neutrophilic infiltration: a vicious circle in inflammatory bowel disease. Gut. 2014, Vol. 63, no.4, pp.578–587. doi:10.1136/gutjnl-2012–303252.
87. Kraan M. C., Haringman J. J., Post W. J., Versendaal J., Breedveld F. C., Tak P. P. Immunohistological analysis of synovial tissue for differential diagnosis in early arthritis. Rheumatology, 1999, Vol. 38, no.11, pp.1074–1080. doi: 10.1093/rheumatology/38.11.1074.
88. Krenn V., Souto-Carneiro M. M., Kim H. J., Berek C., Starostik P., Konig A. Histopathology and molecular pathology of synovial B-lymphocytes in rheumatoid arthritis. Histol. Histopathol., 2000, Vol. 15, pp. 791–798. doi: 10.14670/HH-15.791.
89. Kroenke M. A., Eto D., Locci M., Cho M., Davidson T., Haddad E. K., Crotty S. Bcl6 and Maf cooperate to instruct human follicular helper CD4T cell differentiation. J Immunol., 2012, Vol. 188, no.8, pp.3734–3744. doi: 10.4049/jimmunol. 1103246.
90. Kuivaniemi H., Tromp G. Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases. Gene, 2019. Vol 707, pp. 151–171 https://doi.org/10.1016/j.gene.2019.05.003.
91. Kunnumakkara A. B., Sailo B. L., Banik K., Harsha C., Prasad S…Aggarwal B. B. Chronic diseases, inflammation, and spices: how are they linked? J. Transl. Med., 2018; 16:14. doi: 10.1186/s12967–018–1381–2.
92. Lande R., Gregorio J., Facchinetti V., Chatterjee B., Wang Y. H., Homey B…. Gillet M. Plasmacytoid dendritic cells sense self-DNA coupled with antimicrobial peptide. Nature, 2007, Vol. 449, pp. 564–569. doi: 10.1038/nature06116.
93. Lau C. M., Broughton C., Tabor A. S., Akira S., Flavell R. A., Mamula M…Marshak-Rothstein A. RNA-associated autoantigens activate B cells by combined B cell antigen receptor/Toll-like receptor 7 engagement. J. Exp. Med., 2005, Vol. 202, no.9, pp.1171–1177. doi: 10.1084/jem.20050630.
94. Leadbetter E. A., Rifkin I. R., Hohlbaum A. M., Beaudette B. C., Shlomchik M. J., Marshak-Rothstein A. Chromatin-IgG complexes activate B cells by dual engagement of IgM and Toll-like receptors. Nature, 2002, Vol. 416, pp.603–607.
95. Liao A. P., Salajegheh M., Nazareno R., Kagan J. C., Jubin R. G. Greenberg S. A.. Interferon β is associated with type 1 interferon-inducible gene expression in dermatomyositis. Ann Rheum Dis., 2011, Vol. 70, no.5, pp.831–836. doi: 10.1136/ard.2010.139949.
96. Loo J., Spittle D. A., Newnham M. COVID-19, immunothrombosis and venous thromboembolism: biological mechanisms. Thorax Published Online First: 06 January 2021. doi: 10.1136/thoraxjnl-2020–216243.
97. Ma W-T., Gao F., Gu K., Chen D-K. The Role of Monocytes and Macrophages in Autoimmune Diseases: A Comprehensive Review. Front. Immunol., 2019; 10:1140. doi: 10.3389/fimmu.2019.01140.
98. Malmstrom V., Venalis P., Albrecht I. T cells in myositis. Arthritis Res. Ther., 2012; 14(6), 230. doi.org/10.1186/ar4116.
99. Mantovani A., Sozzani S., Locati M., Allavena P., Sica A. Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol., 2002, Vol. 23, no.11, pp.549–555. doi: 10.1016/s1471–4906(02)02302–5.
100. Manzo A., Bombardieri M., Humby F., Pitzalis C. Secondary and ectopic lymphoid tissue responses in rheumatoid arthritis: from inflammation to autoimmunity and tissue damage/remodeling. Immunol Rev., 2010, Vol. 233, pp.267–285. doi: 10.1111/j.0105–2896.2009.00861.x.
101. Masters S. L., Simon A., Aksentijevich I., Kastner D. L. Horror Autoinflammaticus: The Molecular Pathophysiology of Autoinflammatory Disease. Annu. Rev. Immunol., 2009, Vol. 27, pp.621–668. doi: 10.1146/annurev.immunol.25.022106.141627.
102. McNally A. K., Anderson J. M. Interleukin-4 induces foreign body giant cells from human monocytes/macrophages. Differential lymphokine regulation of macrophage fusion leads to morphological variants of multinucleated giant cells. Am. J. of Pathology, 1995, Vol. 147, no.5, pp. 1487–1499.
103. McNally A. K., Jones J. A., Macewan S. R., Colton E., Anderson J. M. Vitronectin is a critical protein adhesion substrate for IL-4-induced foreign body giant cell formation. Journal of Biomedical Materials Research, 2008, Vol. 86, no. 2, pp. 535–543. doi: 10.1002/jbm.a.31658.
104. Means T. K., Latz E., Hayashi F., Murali M. R., Golenbock D. T., Luster A. D. Human lupus autoantibody-DNA complexes activate DCs through cooperation of CD32 and TLR9. J. Clin. Investig., 2005, Vol. 115, no. 2, pp. 407–417. doi: 10.1172/JCI23025.
105. Miga A., Masters S., Gonzalez M., Noelle R. J. The role of CD40-CD154 interactions in the regulation of cell mediated immunity. Immunological Investigations, 2000, Vol.29, no 2, pp. 111–114. doi: 10.3109/08820130009062292.
106. Miyabe Y., Lian, J., Miyabe, C., Luster, A. D. Chemokines in rheumatic diseases: pathogenic role and therapeutic implications. Nature Reviews Rheumatology, 2019, 15:731–46. doi:10.1038/s41584–019–0323–6.
107. Moghaddas F., Masters S. L. Monogenic autoinflammatory diseases: cytokinopathies. Cytokine, 2015, Vol. 74, no.2, pp.237–246. doi: 10.1016/j.cyto.2015.02.012.
108. Moore B. B., Keane M. P.,