Tolerogenic dendritic cells and their role in transplantation

被引:141
作者
Ezzelarab, Mohamed [1 ]
Thomson, Angus W. [1 ,2 ]
机构
[1] Univ Pittsburgh, Sch Med, Thomas E Starzl Transplantat Inst, Dept Surg, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
Dendritic cells; Antigen presentation; T cells; T regulatory cells; Tolerance; Transplantation; REGULATORY T-CELLS; PERIPHERAL LYMPHOID ORGANS; ACQUIRED THYMIC TOLERANCE; INHIBITORY RECEPTORS ILT3; COLONY-STIMULATING FACTOR; HEART ALLOGRAFT SURVIVAL; TRYPTOPHAN CATABOLISM; HLA-G; CARDIAC ALLOGRAFTS; HEME OXYGENASE-1;
D O I
10.1016/j.smim.2011.06.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pursuit of clinical transplant tolerance has led to enhanced understanding of mechanisms underlying immune regulation, including the characterization of immune regulatory cells, in particular antigen-presenting cells (APC) and regulatory T cells (Treg), that may play key roles in promoting operational tolerance. Dendritic cells (DC) are highly efficient APC that have been studied extensively in rodents and humans, and more recently in non-human primates. Owing to their ability to regulate both innate and adaptive immune responses, DC are considered to play crucial roles in directing the alloimmune response towards transplant tolerance or rejection. Mechanisms via which they can promote central and peripheral tolerance include clonal deletion, the induction of Treg, and inhibition of memory T cell responses. These properties have led to the use of tolerogenic DC as a therapeutic strategy to promote organ transplant tolerance. In rodents, infusion of donor- or recipient-derived tolerogenic DC can extensively prolong donor-specific allograft survival, in association with regulation of the host T cell response. In clinical transplantation, progress has been made in monitoring DC in relation to graft outcome, including studies in operational liver transplant tolerance. Although clinical trials involving immunotherapeutic DC for patients with cancer are ongoing, implementation of human DC therapy in clinical transplantation will require assessment of various critical issues. These include cell isolation and purification techniques, source, route and timing of administration, and combination immunosuppressive therapy. With ongoing non-human primate studies focused on DC therapy, these logistics can be investigated seeking the optimal approaches. The scientific rationale for implementation of tolerogenic DC therapy to promote clinical transplant tolerance is strong. Evaluation of technical and therapeutic logistic issues is an important next step prior to the application of tolerogenic DC in clinical organ transplantation. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:252 / 263
页数:12
相关论文
共 138 条
[1]   Plasmacytoid dendritic cell precursors induce allogeneic T-cell hyporesponsiveness and prolong heart graft survival [J].
Abe, M ;
Wang, ZL ;
de Creus, A ;
Thomson, AW .
AMERICAN JOURNAL OF TRANSPLANTATION, 2005, 5 (08) :1808-1819
[2]   Heterologous immunity provides a potent barrier to transplantation tolerance [J].
Adams, AB ;
Williams, MA ;
Jones, TR ;
Shirasugi, N ;
Durham, MM ;
Kaech, SM ;
Wherry, EJ ;
Onami, T ;
Lanier, JG ;
Kokko, KE ;
Pearson, TC ;
Ahmed, R ;
Larsen, CP .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (12) :1887-1895
[3]   Major histocompatibility complex class I peptide-pulsed host dendritic cells induce antigen-specific acquired thymic tolerance to islet cells [J].
Ali, A ;
Garrovillo, M ;
Jin, MX ;
Hardy, MA ;
Oluwole, SF .
TRANSPLANTATION, 2000, 69 (02) :221-226
[4]   Differential regulation of naive and memory CD4+ T cells by alternatively activated dendritic cells [J].
Anderson, Amy E. ;
Sayers, Bethan L. ;
Haniffa, Muzlifah A. ;
Swan, David J. ;
Diboll, Julie ;
Wang, Xiao-Nong ;
Isaacs, John D. ;
Hilkens, Catharien M. U. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 84 (01) :124-133
[5]   Cellular interactions in thymocyte development [J].
Anderson, G ;
Moore, NC ;
Owen, JJT ;
Jenkinson, EJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :73-99
[6]  
[Anonymous], J TRANSL MED, DOI DOI 10.1186/1479-5876-2-27
[7]   A minor population of splenic dendritic cells expressing CD19 mediates IDO-dependent T cell suppression via type IIFN signaling following B7 ligation [J].
Baban, B ;
Hansen, AM ;
Chandler, PR ;
Manlapat, A ;
Bingaman, A ;
Kahler, DJ ;
Munn, DH ;
Mellor, AL .
INTERNATIONAL IMMUNOLOGY, 2005, 17 (07) :909-919
[8]   Dendritic Cells Secrete the Immunosuppressive HLA-G Molecule upon CTLA4-Ig Treatment: Implication in Human Renal Transplant Acceptance [J].
Bahri, Rajia ;
Naji, Abderrahim ;
Menier, Catherine ;
Charpentier, Bernard ;
Carosella, Edgardo D. ;
Rouas-Freiss, Nathalie ;
Durrbach, Antoine .
JOURNAL OF IMMUNOLOGY, 2009, 183 (11) :7054-7062
[9]   Dendritic cells: Tools and targets for transplant tolerance [J].
Barratt-Boyes, SM ;
Thomson, AW .
AMERICAN JOURNAL OF TRANSPLANTATION, 2005, 5 (12) :2807-2813
[10]   Affects of immunosuppression on circulating dendritic cells: An adjunct to therapeutic drug monitoring after heart transplantation [J].
Barten, Markus J. ;
Garbade, Jens ;
Bittner, Hartmuth B. ;
Fiedler, Martin ;
Dhein, Stefan ;
Thiery, Joachim ;
Mohr, Friedrich W. ;
Gummert, Jan F. .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2006, 6 (13-14) :2011-2017