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Lupus Nephritis: Current Treatment Paradigm and Unmet Needs
被引:24
|作者:
Menez, Steven P.
[1
]
El Essawy, Basset
[2
]
Atta, Mohamed G.
[1
]
机构:
[1] Johns Hopkins Dept Med, Div Nephrol, Baltimore, MD 21287 USA
[2] Al Azhar Univ, Dept Med, Nephrol Unit, Cairo, Egypt
关键词:
Chronic kidney disease;
clinical trials;
End-Stage Renal Disease (ESRD);
immunosuppression;
kidney biopsy;
systemic lupus erythematosus;
D O I:
10.2174/1574887112666171123113200
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Background: Systemic Lupus Erythematosus (SLE) is an autoimmune disorder characterized by chronic inflammation, which can result in a multitude of systemic or organ-limited manifestations, including the skin, lungs, heart, and kidney. SLE nephritis is present in an average of 38% of patients at the time of diagnosis, and may occur as the initial presentation of disease with progression to End-Stage Renal Disease (ESRD) in roughly 10-20% of patients. Methods: A review of the current literature was undertaken to investigate the evolution of treatment of SLE nephritis based on randomized trials and robust observational studies. We aimed to provide a timeline of the development of current induction and maintenance therapy, as well as the development of novel targeted therapies, all leading to current guidelines. Results: Based on all available current data on standard of care therapies for SLE nephritis, there is at best a complete remission rate of 50-60%, and roughly 13-25% of patients experience periods of relapse during maintenance therapy for SLE nephritis. Therefore, the need for newer, targeted therapies has been the focus of many current, ongoing clinical trials. Conclusion: Standard induction and maintenance therapies at present are anti-proliferative and nonspecific, that is, interfering with the process of autoantigen presentation and activation of autoreactive leukocytes. However, newer agents with specific T-cell, B-cell, or proteasome targets are currently being investigated.
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页码:105 / 113
页数:9
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