Dendritic cells, T cell tolerance and therapy of adverse immune reactions

被引:65
作者
Morel, PA
Feili-Hariri, M
Coates, PT
Thomson, AW
机构
[1] Univ Pittsburgh, Med Ctr, Dept Immunol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Med Ctr, Dept Med, Pittsburgh, PA USA
[3] Univ Pittsburgh, Med Ctr, Thomas E Starzl Transplantat Inst, Pittsburgh, PA USA
[4] Univ Pittsburgh, Med Ctr, Dept Surg, Pittsburgh, PA USA
关键词
dendritic cells; tolerance; T cells; transplantation; autoimmunity; allergy;
D O I
10.1046/j.1365-2249.2003.02161.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DC) are uniquely able to either induce immune responses or to maintain the state of self tolerance. Recent evidence has shown that the ability of DC to induce tolerance in the steady state is critical to the prevention of the autoimmune response. Likewise, DC have been shown to induce several type of regulatory T cells including Th2, Tr1, Ts and NKT cells, depending on the maturation state of the DC and the local microenvironment. DC have been shown to have therapeutic value in models of allograft rejection and autoimmunity, although no success has been reported in allergy. Several strategies, including the use of specific DC subsets, genetic modification of DC and the use of DC at various maturation stages for the treatment of allograft rejection and autoimmune disease are discussed. The challenge for the future use of DC therapy in human disease is to identify the appropriate DC for the proposed therapy; a task made more daunting by the extreme plasticity of DC that has recently been demonstrated. However, the progress achieved to date suggests that these are not insurmountable obstacles and that DC may become a useful therapeutic tool in transplantation and autoimmune disease.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 135 条
[1]   Marked increase in number of dendritic cells in autoimmune-prone (NZW x BXSB)F1 mice with age [J].
Adachi, Y ;
Taketani, S ;
Toki, J ;
Ikebukuro, K ;
Sugiura, K ;
Oyaizu, H ;
Yasumizu, R ;
Tomita, M ;
Kaneda, H ;
Amoh, Y ;
Ito, T ;
Okigaki, M ;
Inaba, M ;
Ikehara, S .
STEM CELLS, 2002, 20 (01) :61-72
[2]   Pulmonary dendritic cells producing IL-10 mediate tolerance induced by respiratory exposure to antigen [J].
Akbari, O ;
DeKruyff, RH ;
Umetsu, DT .
NATURE IMMUNOLOGY, 2001, 2 (08) :725-731
[3]  
Akbari O, 2002, NAT MED, V8, P1024, DOI 10.1038/nm745
[4]   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
[5]   The role of dendritic cells, B cells, and M cells in gut-oriented immune responses [J].
Alpan, O ;
Rudomen, G ;
Matzinger, P .
JOURNAL OF IMMUNOLOGY, 2001, 166 (08) :4843-4852
[6]   Origin and differentiation of dendritic cells [J].
Ardavín, C ;
del Hoyo, GM ;
Martín, P ;
Anjuère, F ;
Arias, CF ;
Marín, AR ;
Ruiz, S ;
Parrillas, V ;
Hernández, H .
TRENDS IN IMMUNOLOGY, 2001, 22 (12) :691-700
[7]   Granulocyte-colony stimulating factor mobilizes T helper 2-inducing dendritic cells [J].
Arpinati, M ;
Green, CL ;
Heimfeld, S ;
Heuser, JE ;
Anasetti, C .
BLOOD, 2000, 95 (08) :2484-2490
[8]   Rhesus monocyte-derived dendritic cells modified to over-express TGF-β1 exhibit potent veto activity [J].
Asiedu, C ;
Dong, SS ;
Pereboev, A ;
Wang, WL ;
Navarro, J ;
Curiel, DT ;
Thomas, JM .
TRANSPLANTATION, 2002, 74 (05) :629-637
[9]   THE ROLE OF INDIRECT RECOGNITION IN INITIATING REJECTION OF SKIN-GRAFTS FROM MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II-DEFICIENT MICE [J].
AUCHINCLOSS, H ;
LEE, R ;
SHEA, S ;
MARKOWITZ, JS ;
GRUSBY, MJ ;
GLIMCHER, LH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3373-3377
[10]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+