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Premium Recurrence of HUS Due to CD46/MCP Mutation After Renal Transplantation: A Role for Endothelial Microchimerism
Author(s)
FrémeauxBacchi V.,
Arzouk N.,
Ferlicot S.,
Charpentier B.,
Snanoudj R.,
Dürrbach A.
Publication year2007
Publication title
american journal of transplantation
Resource typeJournals
PublisherBlackwell Publishing Ltd
Mutations in the gene of the membrane cofactor protein (MCP/CD46), a complement regulatory protein, were recently described as a cause of hemolytic uremic syndrome (HUS). MCP is a transmembrane glycoprotein expressed in kidneys; therefore, the transplantation of a normal kidney should not be complicated by HUS recurrence. However, we report the case of a 32‐year‐old woman with an MCP mutation who developed a recurrence of HUS after renal transplantation. We found that she had vascular microchimerism of endothelial cells. We suggest that recurrence may be favored by vascular microchimerism, in which the mutated protein is produced in the in the kidney graft by endothelial cells originating from recipient.
Subject(s)biology , cancer research , fetus , genetics , immunology , medicine , microchimerism , pregnancy , transplantation , urology
Language(s)English
SCImago Journal Rank2.89
H-Index188
eISSN1600-6143
pISSN1600-6135
DOI10.1111/j.1600-6143.2007.01888.x

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