Literature DB >> 1994540

Detection of allograft endothelial cells of recipient origin following ABO-compatible, nonidentical cardiac transplantation.

J B O'Connell1, D G Renlund, M R Bristow, E H Hammond.   

Abstract

Endothelial cells serve an important role in augmenting immune responses through enhanced expression of MHC class II antigens. Immune-mediated vascular injury associated with rejection requires reendothelialization to restore vascular integrity. The origin of the reparative endothelial cells can be determined when ABO antigens expressed on these cells differ in the donor and recipient. To assess the frequency and significance of reendothelialization by recipient endothelial cells, we stained serial endomyocardial biopsies for ABO antigens in 34 (13%) compatible, nonidentical cardiac allograft recipients of 268 cardiac transplant procedures. In ten (30%) the allograft endothelial cells expressed the characteristics of the recipient (five partial and five complete) within 7.5 +/- 1.0 months (mean +/- SEM) after transplantation. Over 26.3 +/- 2.5 months follow-up no differences could be detected in pretransplant characteristics, allograft survival, survivor rejection morbidity, long-term allograft function, and presence of coronary vasculopathy between those whose endothelial cells expressed recipient blood group antigens and those who did not, which may merely be a reflection of the small sample size. This study indicates that recipient reendothelialization occurs frequently following cardiac transplantation and may result from immune-mediated vascular injury. The effect of recipient reendothelialization on allograft tolerance requires further investigation.

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Year:  1991        PMID: 1994540     DOI: 10.1097/00007890-199102000-00033

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  5 in total

Review 1.  The "privileged" liver and hepatic tolerogenicity.

Authors:  T E Starzl
Journal:  Liver Transpl       Date:  2001-10       Impact factor: 5.799

2.  Fluorescence in situ hybridization for the Y-chromosome can be used to detect cells of recipient origin in allografted hearts following cardiac transplantation.

Authors:  R H Hruban; P P Long; E J Perlman; G M Hutchins; W A Baumgartner; K L Baughman; C A Griffin
Journal:  Am J Pathol       Date:  1993-04       Impact factor: 4.307

3.  Origin of neointimal endothelium and alpha-actin-positive smooth muscle cells in transplant arteriosclerosis.

Authors:  J L Hillebrands; F A Klatter; B M van den Hurk; E R Popa; P Nieuwenhuis; J Rozing
Journal:  J Clin Invest       Date:  2001-06       Impact factor: 14.808

4.  Allografts surviving for 26 to 29 years following living-related kidney transplantation: analysis by light microscopy, in situ hybridization for the Y chromosome, and anti-HLA antibodies.

Authors:  P S Randhawa; T Starzl; H C Ramos; M A Nalesnik; J Demetris
Journal:  Am J Kidney Dis       Date:  1994-07       Impact factor: 8.860

Review 5.  Endothelial dysfunction and cardiac allograft vasculopathy.

Authors:  Monica Colvin-Adams; Nonyelum Harcourt; Daniel Duprez
Journal:  J Cardiovasc Transl Res       Date:  2012-11-08       Impact factor: 4.132

  5 in total

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