Literature DB >> 11592088

TGF-beta1 and donor dendritic cells are common key components in donor-specific blood transfusion and anti-class II heart graft enhancement, whereas tolerance induction also required inflammatory cytokines down-regulation.

K Gagne1, S Brouard, M Guillet, M C Cuturi, J P Soulillou, J P Souilillou.   

Abstract

Heart allograft tolerance in adult recipients can be induced in the LEW.1W to LEW.1A congeneic strain combination by pre-graft donor-specific blood transfusion (DST). Long-term survivors accept LEW.1W graft but reject third party skin grafts. As tolerant recipients of heart allografts showed an increase in anti-donor class II antibodies, we hypothesize that these antibodies could be instrumental in tolerance induction. However, anti-donor MHC class II alone prolonged graft survival but did not induce heart allograft tolerance in this combination. We analyzed the immune response patterns in heart allograft recipients following the injection of anti-donor class II antibodies (prolongation) or DST priming (tolerance). As suggested by the different phenomena, several immunological patterns were strikingly different between the two models. In strong contrast to DST-tolerant recipients, at 5 days after transplantation, neither Th1/Th2 nor inflammatory cytokines were inhibited in recipients treated with anti-donor class II antibodies, in which only prolongation of graft survival was induced. Nevertheless, in both models, depletion of resident dendritic cells (DC) from donor hearts inhibited tolerance induction (DST) or shortened allograft survival (anti-donor class II antibodies). Moreover, TGF-beta1 was not down-regulated and administration of neutralizing anti-TGF-beta1 antibody, which inhibited tolerance induction (DST), also shortened allograft survival (anti-donor class II antibodies). These results suggest that, in these two MHC class II-restricted models, both TGF-beta1 and donor DC have a pivotal role in prolonging graft survival. However, in the days following transplantation, further inhibition of inflammatory cytokine production, particularly Th1 and macrophage-derived cytokines is required for tolerance induction.

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Year:  2001        PMID: 11592088     DOI: 10.1002/1521-4141(2001010)31:10<3111::aid-immu3111>3.0.co;2-6

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  5 in total

1.  Upregulation of miR-142-3p in peripheral blood mononuclear cells of operationally tolerant patients with a renal transplant.

Authors:  Richard Danger; Annaïck Pallier; Magali Giral; Marc Martínez-Llordella; Juan José Lozano; Nicolas Degauque; Alberto Sanchez-Fueyo; Jean-Paul Soulillou; Sophie Brouard
Journal:  J Am Soc Nephrol       Date:  2012-01-26       Impact factor: 10.121

2.  Identification of a peripheral blood transcriptional biomarker panel associated with operational renal allograft tolerance.

Authors:  Sophie Brouard; Elaine Mansfield; Christophe Braud; Li Li; Magali Giral; Szu-chuan Hsieh; Dominique Baeten; Meixia Zhang; Joanna Ashton-Chess; Cécile Braudeau; Frank Hsieh; Alexandre Dupont; Annaik Pallier; Anne Moreau; Stéphanie Louis; Catherine Ruiz; Oscar Salvatierra; Jean-Paul Soulillou; Minnie Sarwal
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-14       Impact factor: 11.205

3.  Divergent role of donor dendritic cells in rejection versus tolerance of allografts.

Authors:  Takuya Ueno; Katsunori Tanaka; Mollie Jurewicz; Takaya Murayama; Indira Guleria; Paolo Fiorina; Jesus C Paez; Andrea Augello; Andrea Vergani; Masie Wong; R Neal Smith; Reza Abdi
Journal:  J Am Soc Nephrol       Date:  2009-01-07       Impact factor: 10.121

4.  Recipient natural killer cells alter the course of rejection of allogeneic heart grafts in rats.

Authors:  Oliver Beetz; Joline Kolb; Benjamin Buck; Britta Trautewig; Kai Timrott; Florian W R Vondran; Ingrid Meder; Corinna Löbbert; Joachim Hundrieser; Jürgen Klempnauer; Hüseyin Bektaş; Thorsten Lieke
Journal:  PLoS One       Date:  2019-08-22       Impact factor: 3.240

5.  Immunotoxin Against a Donor MHC Class II Molecule Induces Indefinite Survival of Murine Kidney Allografts.

Authors:  K Brown; A K Nowocin; L Meader; L A Edwards; R A Smith; W Wong
Journal:  Am J Transplant       Date:  2016-01-22       Impact factor: 8.086

  5 in total

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