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Oxidative stress in the pathology and treatment of systemic lupus erythematosus
Open accessAbstract
Oxidative stress is increased in systemic lupus erythematosus (SLE), and it contributes to immune system dysregulation, abnormal activation and processing of cell-death signals, autoantibody production and fatal comorbidities. Mitochondrial dysfunction in T cells promotes the release of highly diffusible inflammatory lipid hydroperoxides, which spread oxidative stress to other intracellular organelles and through the bloodstream. Oxidative modification of self antigens triggers autoimmunity, and the degree of such modification of serum proteins shows striking correlation with disease activity and organ damage in SLE. In T cells from patients with SLE and animal models of the disease, glutathione, the main intracellular antioxidant, is depleted and serine/threonine-protein kinase mTOR undergoes redox-dependent activation. In turn, reversal of glutathione depletion by application of its amino acid precursor, N-acetylcysteine, improves disease activity in lupus-prone mice; pilot studies in patients with SLE have yielded positive results that warrant further research. Blocking mTOR activation in T cells could conceivably provide a well-tolerated and inexpensive alternative approach to B-cell blockade and traditional immunosuppressive treatments. Nevertheless, compartmentalized oxidative stress in self-reactive T cells, B cells and phagocytic cells might serve to limit autoimmunity and its inhibition could be detrimental. Antioxidant therapy might also be useful in ameliorating damage caused by other treatments. This Review thus seeks to critically evaluate the complexity of oxidative stress and its relevance to the pathogenesis and treatment of SLE.
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“In various cell types, metabolic aberrations induced by mitochondrial abnormalities are linked to self-reactive and inflammatory phenotypes in autoimmune conditions, including SLE and RA68,69”
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“These events can lead to the generation of neoantigens that could be recognized as exogenous threats by the adaptive immune system68”
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Cites
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
Cillà, S. D., Farruggio, S., Vujosevic, S., Raina, G., Filippini, D. A., Gatti, V., Clemente, N., Mary, D., Vezzola, D., Casini, G., et al. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479441 · Cited by 5,154
[1] Role of free radicals and catalytic metal ions in human disease: An overview
Halliwell, B., & Gutteridge, J. M. C. (1990) · Methods in Enzymology · doi:10.1016/0076-6879(90)86093-b · Cited by 4,994
Tsokos, G. C. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-37754-6.50094-4 · Cited by 3,990
Targeting the KEAP1-NRF2 system to prevent kidney disease progression
Nezu, M., Suzuki, N., & Yamamoto, M. (2017) · American Journal of Nephrology · doi:10.1159/000475890 · Cited by 3,447
Tsokos, G. C. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1100359 · Cited by 2,814
Manzi, S., Meilahn, E. N., Rairie, J. E., Conte, C. G., Medsger, T. A., Jansen-McWilliams, L., D’Agostino, R. B., & Kuller, L. H. (1997) · American Journal of Epidemiology · doi:10.1093/oxfordjournals.aje.a009122 · Cited by 1,831
Suppression of Oxidative Stress by β-Hydroxybutyrate, an Endogenous Histone Deacetylase Inhibitor
Shimazu, T., Hirschey, M. D., Newman, J., He, W., Shirakawa, K., Le Moan, N., Grueter, C. A., Lim, H., Saunders, L. R., Stevens, R. D., et al. (2013) · Science · doi:10.1126/science.1227166 · Cited by 1,777
Chronic Granulomatous Disease: Report on a National Registry of 368 Patients
Winkelstein, J. A., Marino, M. C., Johnston, R. B., Boyle, J., Curnutte, J., Gallin, J. I., Malech, H. L., Holland, S. M., Ochs, H., Quie, P., et al. (2000) · Medicine · doi:10.1097/00005792-200005000-00003 · Cited by 1,728
Casciola-Rosen, L. A., Anhalt, G. J., & Rosen, A. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.4.1317 · Cited by 1,723
Research works printed but not linked: 2
- Caza, T. N., Talaber, G. & Perl, A. Metabolic regulation of organelle homeostasis in lupus T cells. Clin. Immunol. 144, 200–213 (2012). · DOI
- Dwivedi, J. & Sarkar, P. D. Study of homocysteine, lipoprotein (a), lipid profile with oxidative stress in nephrotic syndrome and lupus nephritis. Res. J. Pharm. Biol. Chem. Sci. 1, 670–679 (2010).
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Perl, A., Hanczko, R., Lai, Z.-W., Oaks, Z., Kelly, R., Borsuk, R., Asara, J. M., & Phillips, P. E. (2015) · Metabolomics · doi:10.1007/s11306-015-0772-0 · Cited by 189
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Zhao, M., Liu, S. M., Luo, S., Wu, H., Tang, M.-N., Cheng, W., Zhang, Q., Zhang, P., Yu, X., Xia, Y., et al. (2014) · Journal of Autoimmunity · doi:10.1016/j.jaut.2014.07.002 · Cited by 185
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Liu, Y., Yu, J., Oaks, Z., Marchena, I., Francis, L., Bonilla, E., Aleksiejuk, P. A., Patel, J., Bánki, K., LANDAS, S. K., et al. (2015) · Clinical Immunology · doi:10.1016/j.clim.2015.07.001 · Cited by 57
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Monaco, A., Ferrandino, I., Boscaino, F., Cocca, E., Cigliano, L., Maurano, F., Luongo, D., Spagnuolo, M. S., Rossi, M., & Bergamo, P. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m079400 · Cited by 57
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Talabér, G., Miklóssy, G., Oaks, Z., Liu, Y., Tooze, S. A., Chudakov, D. M., Bánki, K., & Perl, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084392 · Cited by 52
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Handono, K., Pratama, M. Z., Endharti, A. T., & Kalim, H. (2016) · Central European Journal of Immunology · doi:10.5114/ceji.2015.56970 · Cited by 50
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Blanco, L. P., Patiño‐Martínez, E., Nakabo, S., Zhang, M., Pedersen, H. L., Wang, X., Carmona‐Rivera, C., Claybaugh, D., Yu, Z., Desta, E., et al. (2022) · Arthritis & Rheumatology · doi:10.1002/art.42284 · Cited by 49
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Ren, Y., Jiang, H., Gu, S., Feng, N., Zhang, N., Lv, L., & Liu, F. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.02138 · Cited by 48
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Wang, X., Xu, W., Wang, F., Leng, R., Yang, X., Ling, H., Fan, Y., Tao, J., Shuai, Z., Zhang, L., et al. (2022) · Arthritis & Rheumatology · doi:10.1002/art.42304 · Cited by 47
Wu, T., Ye, Y., Min, S., Zhu, J., Khobahy, E., Zhou, J. K., Yan, M., Hemachandran, S., Pathak, S., Zhou, X., et al. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38782 · Cited by 47
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Gorelik, G. J., Sawalha, A. H., Patel, D. R., Johnson, K. J., & Richardson, B. (2015) · Clinical Immunology · doi:10.1016/j.clim.2015.03.017 · Cited by 47
Lu, L., Hu, C., Zhao, Y., He, L., Zhou, J., Li, H., Du, Y., Wang, Y., Wen, C., Han, X., et al. (2018) · Biomolecules · doi:10.3390/biom8040105 · Cited by 49
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Zheng, X., & Sawalha, A. H. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0066 · Cited by 49
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Limanaqi, F., Biagioni, F., Busceti, C. L., Fabrizi, C., Frati, A., & Fornai, F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051642 · Cited by 48
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Chi, X., Huang, M., Tu, H., Zhang, B., Lin, X., Xu, H., Dong, C., & Hu, X. (2023) · Science China Life Sciences · doi:10.1007/s11427-021-2187-3 · Cited by 47
Yang, D., Su, Z., Wu, S., Bi, Y., Li, X., Li, J., Lou, K., Zhang, H., & Zhang, X. (2015) · International Journal of Neuroscience · doi:10.3109/00207454.2015.1134526 · Cited by 45
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dos Santos, M., Veronese, F. V., & Moresco, R. N. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.05.034 · Cited by 45
Tan, S. Y., Kelkar, Y., Hadjipanayis, A. G., Shipstone, A., Wynn, T. A., & Hall, J. P. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.2000137 · Cited by 46
Fujii, J. (2015) · World Journal of Nephrology · doi:10.5527/wjn.v4.i2.213 · Cited by 44
Tzang, B., Liu, C.-H., Hsu, K.-C., Chen, Y.-H., Huang, C., & Hsu, T. (2017) · British Journal Of Nutrition · doi:10.1017/s0007114517002112 · Cited by 43
Soriano‐Maldonado, A., Morillas‐de‐Laguno, P., Sabio, J. M., Gavilán‐Carrera, B., Rosales‐Castillo, A., Montalbán‐Méndez, C., Sáez‐Urán, L. M., Callejas-Rubio, J. L., & Vargas‐Hitos, J. A. (2018) · Journal of Clinical Medicine · doi:10.3390/jcm7120477 · Cited by 44
Metadata
- Authors
- Perl, A.
- Venue
- Nature Reviews Rheumatology
- Published
- 2013-10-08
- Volume
- 9
- Issue
- 11
- Pages
- 674-686
- ISSN
- 1759-4790 (ISSN-L)
- 1759-4804
- PMC
- PMC4046645
- OpenAlex
- W2078472057
- Cited by
- 358
- References
- 139
- Citations by year
- 2026: 18 · 2025: 44 · 2024: 36 · 2023: 18 · 2022: 28 · 2021: 32 · 2020: 36 · 2019: 27 · 2018: 25 · 2017: 19 · 2016: 33 · 2015: 28 · 2014: 14
- FWCI
- 3.98
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Rheumatology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01AI048079, R01AI072648, AI 048, AI 072)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (U01AR076092)
- National Center for Complementary and Integrative Health (AT-004332, R01AT004332)
- Topics
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- oxidative stress, systemic lupus erythematosus, mitochondrial dysfunction, T cells, lipid hydroperoxides, glutathione depletion, mTOR, N-acetylcysteine, antioxidant therapy, autoimmunity, autoantibody production, disease activity, organ damage, lupus-prone mice
- MeSH terms
- Animals, Antioxidants, Humans, Lupus Erythematosus, Systemic, Autoimmunity, Oxidative Stress
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