Literature DB >> 3103273

Promotion of incompatible allograft acceptance in rhesus monkeys given posttransplant antithymocyte globulin and donor bone marrow. I. In vivo parameters and immunohistologic evidence suggesting microchimerism.

J Thomas, M Carver, P Cunningham, K Park, J Gonder, F Thomas.   

Abstract

This report extends previous studies demonstrating that prolonged acceptance of incompatible kidney allografts in rhesus monkeys can be achieved by a short recipient rabbit antithymocyte globulin (RATG) treatment course followed by donor bone marrow infusion on day 12 without a requirement for chronic immunosuppression. Serial studies of antilymphocyte cyctotoxic antibody in recipients' sera following RATG injections showed pan-lymphocyte-reactive antibody present until day 10 posttransplant. On days 11 and 12, pan-lymphocyte-reactive antibody was no longer detectable, but cytotoxic antibody specific for mature T cells remained in recipients' sera. These findings might explain the critical time relationship between antithymocyte globulin treatment and donor bone marrow infusion, and further suggest that the tolerance-promoting cell in donor bone marrow is not a mature T cell, but rather a pre-T or a non-T cell. Finally, it was found that this treatment protocol resulted in development of lymphoid nodules in the transplanted kidney that express a CD8-positive, FcIgG-receptor-positive phenotype and appear to be of donor origin. The possibility of a veto cell type of mechanism is discussed as an explanation for the promotion of allograft acceptance in this model.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3103273     DOI: 10.1097/00007890-198703000-00002

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


  16 in total

Review 1.  Transplantation tolerance, microchimerism, and the two-way paradigm.

Authors:  T E Starzl; A J Demetris
Journal:  Theor Med Bioeth       Date:  1998-09

Review 2.  Tolerance induction for solid organ grafts with donor-derived hematopoietic reconstitution.

Authors:  K L Gandy
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

3.  History of clinical transplantation.

Authors:  T E Starzl
Journal:  World J Surg       Date:  2000-07       Impact factor: 3.352

4.  The basis of allograft acceptance.

Authors:  Thomas E Starzl
Journal:  Forum (Genova)       Date:  1997

5.  CTLA4-Ig and anti-CD40 ligand prevent renal allograft rejection in primates.

Authors:  A D Kirk; D M Harlan; N N Armstrong; T A Davis; Y Dong; G S Gray; X Hong; D Thomas; J H Fechner; S J Knechtle
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

Review 6.  The future of transplantation: with particular reference to chimerism and xenotransplantation.

Authors:  T E Starzl; A J Demetris; N Murase; L Valdivia; A W Thomson; J Fung; A S Rao
Journal:  Transplant Proc       Date:  1997 Feb-Mar       Impact factor: 1.066

Review 7.  Bidirectional alloreactivity: A proposed microchimerism-based solution to the NIMA paradox.

Authors:  William J Burlingham; Gilles Benichou
Journal:  Chimerism       Date:  2012-04-01

8.  Historical overview of transplantation.

Authors:  Clyde F Barker; James F Markmann
Journal:  Cold Spring Harb Perspect Med       Date:  2013-04-01       Impact factor: 6.915

Review 9.  The dichotomous functions of passenger leukocytes in solid-organ transplantation.

Authors:  A J Demetris; N Murase; A S Rao; J J Fung; T E Starzl
Journal:  Adv Nephrol Necker Hosp       Date:  1995

10.  Pulmonary angiography for the diagnosis of thromboembolic events in the non-human primate.

Authors:  Ziv Neeman; Boaz Hirshberg; Michael G Tal; Bradford J Wood; David M Harlan
Journal:  Transplantation       Date:  2004-10-15       Impact factor: 4.939

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.