Targeted complement inhibition as a promising strategy for preventing inflammatory complications in hemodialysis

被引:55
作者
DeAngelis, Robert A. [1 ]
Reis, Edimara S. [1 ]
Ricklin, Daniel [1 ]
Lambris, John D. [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
Complement; Hemodialysis; Inflammation; Therapeutics; Innate immunity; NECROSIS-FACTOR-ALPHA; COATED CARDIOPULMONARY BYPASS; MODEL BIOMATERIAL SURFACE; HUMAN C4B-BINDING PROTEIN; STREPTOCOCCAL M-PROTEIN; CHRONIC KIDNEY-DISEASE; CHRONIC-RENAL-FAILURE; FACTOR-H; ALTERNATIVE PATHWAY; DIALYSIS PATIENTS;
D O I
10.1016/j.imbio.2012.07.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Hemodialysis is the most common method used to remove waste and hazardous products of metabolism in patients suffering from renal failure. Hundreds of thousands of people with end-stage renal disease undergo hemodialysis treatment in the United States each year. Strikingly, the 5-year survival rate for all dialysis patients is only 35%. Most of the patients succumb to cardiovascular disease that is exacerbated by the chronic induction of inflammation caused by contact of the blood with the dialysis membrane. The complement system, a strong mediator of pro-inflammatory networks, is a key contributor to such biomaterial-induced inflammation. Though only evaluated in experimental ex vivo settings, specific targeting of complement activation during hemodialysis has uncovered valuable information that points toward the therapeutic use of complement inhibitors as a means to control the unwelcomed inflammatory responses and consequent pathologies in hemodialysis patients. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1097 / 1105
页数:9
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