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Critical Reviews™ in Immunology

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ISSN Imprimir: 1040-8401

ISSN On-line: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

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Metabolic Factors that Contribute to Lupus Pathogenesis

Volume 36, Edição 1, 2016, pp. 75-98
DOI: 10.1615/CritRevImmunol.2016017164
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Wei Li
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610; Department of Biochemistry and Molecular Biology, Gene Engineering and Biotechnology, Beijing Key Laboratory, Beijing Normal University, Beijing 100875, People's Republic of China
Ramya Sivakumar
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610
Anton A. Titov
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610
Seung-Chul Choi
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610
Laurence Morel
Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL 32610

RESUMO

Systemic lupus erythematosus (SLE) is an autoimmune disease in which organ damage is mediated by pathogenic autoantibodies directed against nucleic acids and protein complexes. Studies in SLE patients and in mouse models of lupus have implicated virtually every cell type in the immune system in the induction or amplification of the autoimmune response as well as the promotion of an inflammatory environment that aggravates tissue injury. Here, we review the contribution of CD4+ T cells, B cells, and myeloid cells to lupus pathogenesis and then discuss alterations in the metabolism of these cells that may contribute to disease, given the recent advances in the field of immunometabolism.

Palavras-chave: lupus, autoimmunity, T cells, B cells, myeloid cells, immunometabolism
CITADO POR

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  5. Zhou Zhou, Tian Zhiqiang, Zhang Mengjie, Zhang Yuxun, Ni Bing, Hao Fei, Upregulated IL-1 Receptor-associated Kinase 1 (IRAK1) in Systemic Lupus Erythematosus: IRAK1 Inhibition Represses Th17 Differentiation with Therapeutic Potential, Immunological Investigations, 47, 5, 2018. Crossref

  6. Sivakumar Ramya, Abboud Georges, Mathews Clayton E., Atkinson Mark A., Morel Laurence, Protective Role of Myeloid Cells Expressing a G-CSF Receptor Polymorphism in an Induced Model of Lupus, Frontiers in Immunology, 9, 2018. Crossref

  7. Ren Jingjing, Panther Eric, Liao Xiaofeng, Grammer Amrie, Lipsky Peter, Reilly Chris, The Impact of Protein Acetylation/Deacetylation on Systemic Lupus Erythematosus, International Journal of Molecular Sciences, 19, 12, 2018. Crossref

  8. Gaber Timo, Chen Yuling, Krauß Pierre-Louis, Buttgereit Frank, Metabolism of T Lymphocytes in Health and Disease, in Biology of T Cells - Part B, 342, 2019. Crossref

  9. Lee Michael H., Chakhtoura Marita, Sriram Uma, Caricchio Roberto, Gallucci Stefania, Conventional DCs from Male and Female Lupus-Prone B6.NZM Sle1/Sle2/Sle3 Mice Express an IFN Signature and Have a Higher Immunometabolism That Are Enhanced by Estrogen, Journal of Immunology Research, 2018, 2018. Crossref

  10. Tsai Chang-Youh, Shen Chieh-Yu, Liao Hsien-Tzung, Li Ko-Jen, Lee Hui-Ting, Lu Cheng-Shiun, Wu Cheng-Han, Kuo Yu-Min, Hsieh Song-Chou, Yu Chia-Li, Molecular and Cellular Bases of Immunosenescence, Inflammation, and Cardiovascular Complications Mimicking “Inflammaging” in Patients with Systemic Lupus Erythematosus, International Journal of Molecular Sciences, 20, 16, 2019. Crossref

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  12. Sundberg John P., Silva Kathleen A., Kennedy Victoria E., Wilson John J., Gott Nicholas E., Sundberg Beth A., Roopenian Derry C., 2‐deoxy D‐glucose treatment does not elicit a hair growth response in alopecia areata, Experimental Dermatology, 28, 9, 2019. Crossref

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  14. Li Jun, Ding Huihua, Meng Yao, Li Guanhua, Fu Qiong, Guo Qiang, Yin Zhihua, Ye Zhizhong, Zhou Haibo, Shen Nan, Taurine Metabolism Aggravates the Progression of Lupus by Promoting the Function of Plasmacytoid Dendritic Cells, Arthritis & Rheumatology, 72, 12, 2020. Crossref

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  20. Pan Tingting, Sun Shaoqiong, Chen Yang, Tian Rui, Chen Erzhen, Tan Ruoming, Wang Xiaoli, Liu Zhaojun, Liu Jialin, Qu Hongping, Immune effects of PI3K/Akt/HIF-1α-regulated glycolysis in polymorphonuclear neutrophils during sepsis, Critical Care, 26, 1, 2022. Crossref

  21. Robinson George Anthony, Wilkinson Meredyth G. Ll., Wincup Chris, The Role of Immunometabolism in the Pathogenesis of Systemic Lupus Erythematosus, Frontiers in Immunology, 12, 2022. Crossref

  22. Becker Yann L. C., Duvvuri Bhargavi, Fortin Paul R., Lood Christian, Boilard Eric, The role of mitochondria in rheumatic diseases, Nature Reviews Rheumatology, 2022. Crossref

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