Скачать книгу

no.4, pp.624–632. doi: 10.1038/cdd.2009.197.

      45. De Paepe B., Creus K. K., De Bleecker J. L. Chemokines in idiopathic inflammatory myopathies. Front. Biosci., 2008, Vol. 13, pp. 2548–2577. DOI: 10.2741/2866.

      46. De Paepe B., Creus K. K., De Bleecker J. L. Role of cytokines and chemokines in idiopathic inflammatory myopathies. Curr. Opin. Rheumatol., 2009, Vol. 21, no.6, pp.610–616. DOI: 10.1097/bor.0b013e3283317b31.

      47. Decker P., Kotter I., Klein R., Berner B., Rammensee H. G. Monocyte-derived dendritic cells over-express CD86 in patients with systemic lupus erythematosus. Rheumatology, 2006, Vol. 45, no.9, pp.1087–1095. doi: 10.1093/rheumatology/kel061.

      48. Dennis G. Jr., Holweg C. T., Kummerfeld S. K., Choy D. F., Setiadi A. F., Hackney J.A…Townsend M.. Synovial phenotypes in rheumatoid arthritis correlate with response to biologic therapeutics. Arthr. Res. Ther., 2014, Vol.16, no.2, R90. doi: 10.1186/ar4555.

      49. Dieguez-Gonzalez R., Calaza M., Perez-Pampin E. Association of interferon regulatory factor 5 haplotypes, similar to that found in systemic lupus erythematosus, in a large subgroup of patients with rheumatoid arthritis. Arthritis Rheum., 2008, Vol. 58, no.5, pp.1264–1274. doi: 10.1002/art.2342.

      50. Doster R. S., Rogers L. M., Gaddy J. A., Aronoff D. M. Macrophage Extracellular Traps: A Scoping Review. J. Innate Immun., 2017, Vol.10, no.1, pp.3–13. doi: 10.1159/000480373.

      51. Ek M., Popovic K., Harris H. E., Naucler C. S., Wahren-Herlenius M. Increased extracellular levels of the novel proinflammatory cytokine high mobility group box chromosomal protein 1 in minor salivary glands of patients with Sjogren’s syndrome. Arthritis Rheum., 2006, Vol. 54, no. 7, pp.2289–2294. doi: 10.1002/art.21969.

      52. Eming S. A., Wynn T. A., Martin P. Inflammation and metabolism in tissue repair and regeneration. Science, 2017, Vol.356, pp.1026–1030. doi: 10.1126/science.aam7928.

      53. Fang C., Luo T., Lin, L. The correlational research among serum CXCL13 levels, circulating plasmablasts and memory B cells in patients with systemic lupus erythematosus: a STROBE-compliant article. Medicine, 2017, 96(48), e8675. doi: 10.1097/MD.0000000000008675.

      54. Feng D., Sangster-Guity N., Stone R., Korczeniewska J… Mancl M. E., Fitzgerald-Bocarsly P., Barnes B. J. Differential requirement of histone acetylase and deacetylase activities for IRF5-mediated proinflammatory cytokine expression. J. Immunol., 2010, Vol. 185, no.10, pp.6003–6012. doi: 10.4049/jimmunol.1000482.

      55. Fernando M. A., Stevens C. R., Walsh E. C., Jager F., Goyette P., Plenge R., Vyse T., Rioux J.. Defining the Role of the MHC in Autoimmunity: A Review and Pooled Analysis. PLoS Genet 4(4): e1000024. doi:10.1371/journal.pgen.1000024.

      56. Firestein G. S. Invasive fibroblast-like synoviocytes in rheumatoid arthritis. Passive responders or transformed aggressors? Arthritis Rheum., 1996, Vol. 39, no.11, pp. 1781–1790. doi: 10.1002/art.1780391103.

      57. Garcia-Romo G. S., Caielli S., Vega B., Connolly J., Allantaz F….Pascual V. Netting neutrophils are major inducers of type I IFN production in pediatric systemic lupus erythematosus. Sci. Transl. Med., 2011, Vol. 3, issue73, 73ra20. doi: 10.1126/scitranslmed.3001201.

      58. Gregersen P. K., Silver J., Winchester R. J. The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis. Arthritis Rheumatol., 1987, Vol. 30, no.11, pp.1205–1213. doi: 10.1002/art.1780301102.

      59. Griffith, J. W., Sokol C. L., Luster A. D. Chemokines and chemokine receptors: positioning cells for host defense and immunity. Annu. Rev. Immunol., 2014, Vol. 32, pp. 659–702. doi: 10.1146/annurev-immunol-032713–120145.

      60. Gross H., Hennard C., Masouris I., Cassel C., Barth S. Binding of the heterogeneous ribonucleoprotein K (hnRNP K) to the Epstein-Barr virus nuclear antigen 2 (EBNA2) enhances viral LMP2A expression. 2012; PLOS ONE 7:e42106.

      61. Gupta A. K., Joshi M. B., Philippova M., Erne P., Hasler P., Hahn S., Resink T. J. Activated endothelial cells induce neutrophil extracellular traps and are susceptible to NETosis-mediated cell death. FEBS Lett., 2010; 584, pp.3193–3197. doi: 10.1016/j.febslet.2010.06.006.

      62. Hase K., Tani K., Shimizu T, Ohmoto Y., Matsushima K., Sone S. Increased CCR4 expression in active systemic Lupus erythematosus. J. Leukocyte Biol., 2001, Vol. 70, pp. 749.

      63. Helming L., Gordon S. Molecular mediators of macrophage fusion. Trends Cell Biol., 2009, Vol. 19, no.5, pp.514–522. doi: 10.1016/j.tcb.2009.07.005.

      64. Hernandez-Molina G., Michel-Peregrina M., Hernandez-Ramirez D. F., Sanchez-Guerrero J., Llorente L. Chemokine saliva levels in patients with primary Sjogren’s syndrome, associated Sjogren’s syndrome, pre-clinical Sjogren’s syndrome and systemic autoimmune diseases. Rheumatology, 2011, Vol. 50, no.7, pp.1288–1292. doi: 10.1093/rheumatology/ker019.

      65. Herrmann M., Voll R. E., Zoller O. M., Hagenhofer M., Ponner B. B., Kalden J. R. Impaired phagocytosis of apoptotic cell material by monocyte-derived macrophages from patients with systemic lupus erythematosus. Arthritis Rheum.,1998, Vol.41, no.7, pp.:1241–1250. doi: 10.1002/1529- 0131(199807)41:7<1241::AID-ART15>3.0.CO;2-H.

      66. Higashi-Kuwata N., Makino T., Inoue Y., Takeya M., Ihn H. Alternatively activated macrophages (M2 macrophages) in the skin of patient with localized scleroderma. Exp Dermatol., 2009, Vol. 18, no.8, pp.727–729. doi: 10.1111/j.1600–0625.2008.00828.x.

      67. Higgs B. W., Liu Z., White B., Zhu W., White W., Morehouse C….Yao Y.. Patients with systemic lupus erythematosus, myositis, rheumatoid arthritis and scleroderma share activation of a common type I interferon pathway. Ann. Rheum. Dis., 2011, Vol.70, no. 11, pp. 2029–2036. doi: 10.1136/ard.2011.150326.

      68. HjelmstroÈm P. Lymphoid neogenesis – de novo formation of lymphoid tissue in chronic inflammation through expression of homing chemokines. J. Leuk. Biol., 2001, Vol.69, pp.331–339. doi: 10.1097/BOR.0b013e32835fd8eb.

      69. HjelmstroÈm P., Fjell J., Nakagawa T., Sacca R., Cuff C. A., Ruddle N. H. Lymphoid tissue homing chemokines are expressed in chronic inflammation. Am. J. Pathol., 2000, Vol.156, no.4, pp.1133–1138. doi: 10.1016/S0002–9440(10)64981–4.

      70. Horikawa S., Ishii Y., Hamashima T., Yamamoto S., Mori H., Fujimori T….Sasahara M.. PDGFRα plays a crucial role in connective tissue remodeling. Scientific RepoRts., 2015; 5:17948. doi: 10.1038/srep17948.

      71. Humby F., Bombardieri M., Manzo A., Kelly S., Blades M. C., Kirkham B. Ectopic lymphoid structures support ongoing production of class- switched autoantibodies in rheumatoid synovium. PLoS Med. 2009; 6:e1. doi: 10.1371/journal.pmed.0060001.

      72. Jara L. J., Medina. G., Saavedra M. A. Autoimmune manifestations of infections. Curr Opin. Rheumatol. 2018, Vol. 30, no.46, pp.373–379. DOI:10.1097/BOR.0000000000000505.

      73. Jego G., Palucka A. K., Blanck J. P., Chalouni C., Pascual V., Banchereau J. Plasmacytoid dendritic cells induce plasma cell differentiation through type I interferon and interleukin 6. Immunity, 2003, Vol. 19, no.2, pp.225–234. doi: 10.1016/s1074–7613(03)00208–5.

      74. Jenkins M. K., Khoruts A., Ingulli E., Mueller D. L., McSorley S. J., Reinhardt R., Itano A., Pape A. In vivo activation of antigen- specific CD4 T cells. Annu. Rev. Immunol., 2001, Vol.19, pp. 23–45. doi: 10.1146/annurev.immunol.19.1.23.

      75. Jesus A. A., Goldbach-Mansky R. IL-1 blockade in autoinflammatory syndromes. Annu. Rev. Med., 2014, Vol. 65, pp.223–244. doi: 10.1146/annurev-med-061512–150641.

      76. Jorch S., Kubes P. An emerging role for neutrophil extracellular traps in noninfectious disease. NATURE MEDICINE, 2017, Vol. 23, no.3, pp. 279–287. doi:10.1038/nm.4294.

      77. Jurewicz М. М., Stern. L. G. Class II MHC antigen processing in immune tolerance and inflammation. Immunogenetics, 2019,

Скачать книгу