Apoptotic cells induce tolerance by generating helpless CD8+ T cells that produce TRAIL

被引:74
作者
Griffith, Thomas S.
Kazama, Hirotaka
VanOosten, Rebecca L.
Earle, James K., Jr.
Herndon, John M.
Green, Douglas R.
Ferguson, Thomas A.
机构
[1] Washington Univ, Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
[2] Univ Iowa, Dept Urol, Iowa City, IA 52242 USA
[3] Univ Iowa, Interdisciplinary Grad Program Immunol, Iowa City, IA 52242 USA
[4] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
关键词
D O I
10.4049/jimmunol.178.5.2679
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 decision to generate a productive immune response or immune tolerance following pathogenic insult often depends on the context in which T cells first encounter Ag. The presence of apoptotic cells favors the induction of tolerance, whereas immune responses generated with necrotic cells promote immunity. We have examined the tolerance induced by injection of apoptotic cells, a system in which cross-presentation of Ag associated with the dead cells induces CD8(+) regulatory (or suppressor) T cells. We observed that haptenated apoptotic cells induced CD8(+) suppressor T cells without priming CD4(+) T cells for immunity. These CD8(+) T cells transferred unresponsiveness to naive recipients. In contrast, haptenated necrotic cells stimulated immunity, but induced CD8(+) suppressor T cells when CD4(+) T cells were absent. We further found that CD8(+) T cells induced by these treatments displayed a "helpless CIL" phenotype and suppress the immune response by producing TRAIL. Animals deficient in TRAIL were resistant to tolerance induction by apoptotic cells. Thus, the outcome of an immune response taking place in the presence of cell death can be determined by the presence of CD4(+) -mediated Th cell function.
引用
收藏
页码:2679 / 2687
页数:9
相关论文
共 62 条
[1]   Dendritic cell maturation is required for the cross-tolerization of CD8+ T cells [J].
Albert, ML ;
Jegathesan, M ;
Darnell, RB .
NATURE IMMUNOLOGY, 2001, 2 (11) :1010-1017
[2]   Necrotic but not apoptotic cell death releases heat shock proteins, which deliver a partial maturation signal to dendritic cells and activate the NF-κB pathway [J].
Basu, S ;
Binder, RJ ;
Suto, R ;
Anderson, KM ;
Srivastava, PK .
INTERNATIONAL IMMUNOLOGY, 2000, 12 (11) :1539-1546
[3]   DUAL IMMUNOLOGICAL UNRESPONSIVENESS INDUCED BY CELL MEMBRANE COUPLED HAPTEN OR ANTIGEN [J].
BATTISTO, JR ;
BLOOM, BR .
NATURE, 1966, 212 (5058) :156-&
[4]   The CD8α+ dendritic cell is responsible for inducing peripheral self-tolerance to tissue-associated antigens [J].
Belz, GT ;
Behrens, GMN ;
Smith, CM ;
Miller, JFAP ;
Jones, C ;
Lejon, K ;
Fathman, CG ;
Mueller, SN ;
Shortman, K ;
Carbone, FR ;
Heath, WR .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (08) :1099-1104
[5]   Induction of a CD8(+) cytotoxic T lymphocyte response by cross-priming requires cognate CD4(+) T cell help [J].
Bennett, SRM ;
Carbone, FR ;
Karamalis, F ;
Miller, JFAP ;
Heath, WR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :65-70
[6]   VACCINATION AGAINST AUTOIMMUNE ENCEPHALOMYELITIS WITH LYMPHOCYTE-T LINE CELLS REACTIVE AGAINST MYELIN BASIC-PROTEIN [J].
BENNUN, A ;
WEKERLE, H ;
COHEN, IR .
NATURE, 1981, 292 (5818) :60-61
[7]   Human CD8+ T cell blasts are more sensitive than CD4+ T cell blasts to regulation by APO2L/TRAIL [J].
Bosque, A ;
Pardo, J ;
Martínez-Lorenzo, MJ ;
Lasierra, P ;
Larrad, L ;
Marzo, I ;
Naval, J ;
Anel, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (06) :1812-1821
[8]   TGF-β released by apoptotic T cells contributes to an immunosuppressive milieu [J].
Chen, WJ ;
Frank, ME ;
Jin, WW ;
Wahl, SM .
IMMUNITY, 2001, 14 (06) :715-725
[9]  
COHEN JJ, 1993, IMMUNOL TODAY, V14, P126, DOI 10.1016/0167-5699(93)90214-6
[10]   TRAIL-R as a negative regulator of innate immune cell responses [J].
Diehl, GE ;
Yue, HH ;
Hsieh, K ;
Kuang, AA ;
Ho, M ;
Morici, LA ;
Lenz, LL ;
Cado, D ;
Riley, LW ;
Winoto, A .
IMMUNITY, 2004, 21 (06) :877-889