Literature DB >> 15307826

CD154 blockade for induction of mixed chimerism and prolonged renal allograft survival in nonhuman primates.

Tatsuo Kawai1, Hiroshi Sogawa, Svetlan Boskovic, Gregory Abrahamian, Rex-Neal Smith, Siew-Lin Wee, David Andrews, Ognjenka Nadazdin, Ichiro Koyama, Megan Sykes, Henry J Winn, Robert B Colvin, David H Sachs, A Benedict Cosimi.   

Abstract

Costimulatory blockade with anti-CD154 monoclonal antibody (aCD154) prolongs allograft survival in nonhuman primates, but has not reliably induced tolerance when used alone. In the current studies, we evaluated the effect of adding CD154 blockade to a chimerism inducing nonmyeloablative regimen in primates. We observed a significant improvement of donor bone marrow (DBM) engraftment, which has been associated with a lower incidence of acute rejection and long-term survival of renal allografts without the need for previously required splenectomy. Among the long-term survivors, four never showed evidence of rejection, with the longest survival exceeding 1700 days following discontinuation of immunosuppression. Nevertheless, late chronic rejection was observed in three of eight recipients, indicating the necessity of further modifications of the regimen. Control recipients receiving no DBM or donor splenocytes in place of DBM rejected their allografts. Thus, DBM engraftment with, at least, transient mixed chimerism appears essential for induction of allograft tolerance using this conditioning regimen. Modification of the original mixed chimerism approach, by the addition of costimulatory blockade, has been shown to enhance mixed chimerism and induce renal allograft tolerance with less morbidity in nonhuman primates. Copyright 2004 Blackwell Munksgaard

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Year:  2004        PMID: 15307826     DOI: 10.1111/j.1600-6143.2004.00523.x

Source DB:  PubMed          Journal:  Am J Transplant        ISSN: 1600-6135            Impact factor:   8.086


  101 in total

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4.  Contributions of direct and indirect alloresponses to chronic rejection of kidney allografts in nonhuman primates.

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7.  Depletion of CD8 memory T cells for induction of tolerance of a previously transplanted kidney allograft.

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