| Literature DB >> 14520015 |
P Chowdhury1, W Zhou, S H Sacks.
Abstract
Previous research and therapy in renal transplantation largely focused on the cellular arm of the adaptive immune response. Evidence is emerging that innate immune mechanisms, particularly complement, play a greater role in inflammatory and immune responses against the graft than has been previously recognized. Alternative complement pathway activation appears to mediate renal ischaemia/reperfusion injury, and proximal tubular cells may be both the source and the site of attack of complement components in this setting. Locally produced complement also plays a role in the development of both cellular and antibody-mediated immune responses against the graft. C4d staining has emerged as a useful marker of humoral rejection both in the acute and in the chronic setting and led to renewed interest in the significance of anti-donor antibody formation. A number of therapies are in development which inhibit complement or reduce local synthesis, and may lead to an improved clinical outcome following renal transplantation. Copyright 2003 S. Karger AG, BaselEntities:
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Year: 2003 PMID: 14520015 DOI: 10.1159/000073012
Source DB: PubMed Journal: Nephron Clin Pract ISSN: 1660-2110