The Immune System and Idiopathic Nephrotic Syndrome

被引:22
作者
Campbell, Ruth E. E. [1 ]
Thurman, Joshua M. M. [1 ,2 ]
机构
[1] Univ Colorado, Div Renal Dis & Hypertens, Sch Med, Aurora, CO USA
[2] Univ Colorado Anschutz, Renal Div, RC2,12700 East 19th Ave, Aurora, CO 80045 USA
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2022年 / 17卷 / 12期
关键词
immunology; focal segmental glomerulosclerosis; idiopathic nephrotic syndrome; FOCAL SEGMENTAL GLOMERULOSCLEROSIS; GLOMERULAR-PERMEABILITY FACTOR; MINIMAL-CHANGE DISEASE; T-CELL; LYMPHOCYTE POPULATIONS; CLINICAL-SIGNIFICANCE; UROKINASE RECEPTOR; URINARY CD80; RITUXIMAB; PODOCYTES;
D O I
10.2215/CJN.07180622
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Idiopathic nephrotic syndrome often responds to immunosuppressive treatment. Nevertheless, this syndrome?and the drugs used to treat it?remain important causes of patient morbidity. Idiopathic nephrotic syndrome is usually caused by minimal change disease or FSGS, diseases that primarily affect the podocytes. In spite of decades of research, the underlying causes of both diseases remain incompletely understood. There is, however, a large body of observational and experimental data linking the immune system with both minimal change disease and FSGS, including associations with systemic infections and hematologic malignancies. Perhaps most compellingly, many different immunomodulatory drugs are effective for treating idiopathic nephrotic syndrome, including biologic agents that have well-defined immune targets. In fact, the unexpected efficacy of targeted therapeutic agents has provided important new insights into the pathogenesis of these diseases. Given the large number of drugs that are available to deplete or block specific cells and molecules within the immune system, a better understanding of the immunologic causes of idiopathic nephrotic syndrome may lead to better diagnostic and therapeutic approaches.
引用
收藏
页码:1823 / 1834
页数:12
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