Literature DB >> 10489127

Prediction of graft prolongation by mixed lymphocyte culture following anti-CD4 monoclonal antibody treatment among different donor-recipient combinations.

K Hamano1, H Ito, B Shirasawa, H Gohra, T Katoh, Y Fujimura, K Esato.   

Abstract

This study was conducted to examine whether mixed lymphocyte culture (MLC) could be used as a predictor of the efficacy of anti-CD4 monoclonal antibody (MAb) immunosuppression in vivo in a mouse model. C57BL/10 or BALB/c hearts were transplanted into C3H.He recipients. Anti-CD4 MAb administration prolonged graft survival, but there was a clear difference between the two donor-recipient combinations studied, the median survival time (MST) being >100 days in the C57BL/10 --> C3H group, and 17 days in the BALB/c --> C3H group. Anti-CD8 MAb prolonged the survival of C57BL/10 hearts slightly to a MST of 22 days, but the BALB/c hearts were rejected at control rates. Combining anti-CD4 and anti-CD8 antibody therapy prolonged the survival of C57BL/10 hearts indefinitely, but had little effect on the survival of BALB/c grafts, achieving an MST of only 24 days. Next, MLCs were performed in the presence and absence of the MAbs and compared with the graft survival data. The inhibition rates in the MLC, being the C3H lymph node cell responder, correlated well with graft survival. When three kinds of C3H responder cells, namely lymph node (LN) cells, T cells, and CD4+ cells, were examined to determine which was the most suitable for predicting graft survival, the MLC results showed that the responses of LN cells correlated most closely with graft outcome. In conclusion, MLC using LN cells as the responder is a useful tool for predicting allograft survival induced by anti-CD4 MAb therapy.

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Year:  1999        PMID: 10489127     DOI: 10.1007/BF02482777

Source DB:  PubMed          Journal:  Surg Today        ISSN: 0941-1291            Impact factor:   2.549


  22 in total

1.  Evidence that long-term cardiac allograft survival induced by anti-CD4 monoclonal antibody does not require depletion of CD4+ T cells.

Authors:  C R Darby; P J Morris; K J Wood
Journal:  Transplantation       Date:  1992-09       Impact factor: 4.939

2.  Mixed lymphocyte reaction and graft survival in forty cadaveric renal transplants.

Authors:  P R Cullen; S Lester; J Rouch; P J Morris
Journal:  Clin Exp Immunol       Date:  1977-05       Impact factor: 4.330

3.  Assessment of primarily vascularized cardiac allografts in mice.

Authors:  R A Superina; W N Peugh; K J Wood; P J Morris
Journal:  Transplantation       Date:  1986-08       Impact factor: 4.939

4.  Transplantation tolerance induced by CTLA4-Ig.

Authors:  T C Pearson; D Z Alexander; K J Winn; P S Linsley; R P Lowry; C P Larsen
Journal:  Transplantation       Date:  1994-06-27       Impact factor: 4.939

5.  Evidence that the continued presence of the organ graft and not peripheral donor microchimerism is essential for maintenance of tolerance to alloantigen in vivo in anti-CD4 treated recipients.

Authors:  K Hamano; M A Rawsthorne; A R Bushell; P J Morris; K J Wood
Journal:  Transplantation       Date:  1996-09-27       Impact factor: 4.939

6.  Induction of transplantation tolerance in adults using donor antigen and anti-CD4 monoclonal antibody.

Authors:  T C Pearson; J C Madsen; C P Larsen; P J Morris; K J Wood
Journal:  Transplantation       Date:  1992-09       Impact factor: 4.939

7.  The induction of skin graft tolerance in major histocompatibility complex-mismatched or primed recipients: primed T cells can be tolerized in the periphery with anti-CD4 and anti-CD8 antibodies.

Authors:  S P Cobbold; G Martin; H Waldmann
Journal:  Eur J Immunol       Date:  1990-12       Impact factor: 5.532

8.  Induction of donor-specific unresponsiveness to cardiac allografts in rats by pretransplant anti-CD4 monoclonal antibody therapy.

Authors:  J A Shizuru; K B Seydel; T F Flavin; A P Wu; C C Kong; E G Hoyt; N Fujimoto; M E Billingham; V A Starnes; C G Fathman
Journal:  Transplantation       Date:  1990-09       Impact factor: 4.939

9.  The detection of cytotoxic T cells with high-affinity receptors for donor antigens in the transplanted heart as a prognostic factor for graft rejection.

Authors:  A J Ouwehand; C C Baan; D L Roelen; L M Vaessen; A H Balk; N H Jutte; E Bos; F H Claas; W Weimar
Journal:  Transplantation       Date:  1993-11       Impact factor: 4.939

10.  A monoclonal alloantibody detecting a polymorphism of the rat leucocyte common (LC) antigen.

Authors:  M R Newton; K J Wood; J W Fabre
Journal:  J Immunogenet       Date:  1986-02
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