Activation of CD1d-restricted T cells protects NOD mice from developing diabetes by regulating dendritic cell subsets

被引:243
作者
Naumov, YN
Bahjat, KS
Gausling, R
Abraham, R
Exley, MA
Koezuka, Y
Balk, SB
Strominger, JL
Clare-Salzer, M [1 ]
Wilson, SB
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Univ Florida, Coll Med, Dept Pathol, Gainesville, FL 32610 USA
[3] Mayo Clin, Dept Immunol, Rochester, MN 55905 USA
[4] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Canc Biol Program, Boston, MA 02215 USA
[5] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Gunma, Japan
[6] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1073/pnas.251531798
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD1d-restricted invariant NKT (iNKT) cells are immunoregulatory cells whose loss exacerbates diabetes in nonobese diabetic (NOD) female mice. Here, we show that the relative numbers of iNKT cells from the pancreatic islets of NOD mice decrease at the time of conversion from peri-insulitis to invasive insulitis and diabetes. Conversely, NOD male mice who have a low incidence of diabetes showed an increased frequency of iNKT cells. Moreover, administration of alpha -galactosylceramide, a potent activating ligand presented by CD1d, ameliorated the development of diabetes in NOD female mice and resulted in the accumulation of iNKT cells and myeloid dendritic cells (DC) in pancreatic lymph nodes (PLN), but not in inguinal lymph nodes. Strikingly, injection of NOD female mice with myeloid DC isolated from the PLN, but not those from the inguinal lymph nodes, completely prevented diabetes. Thus, the immunoregulatory role of iNKT cells is manifested by the recruitment of tolerogenic myeloid DC to the PLN and the inhibition of ongoing autoimmune inflammation.
引用
收藏
页码:13838 / 13843
页数:6
相关论文
共 43 条
[1]   Checkpoints in the progression of autoimmune disease: Lessons from diabetes models [J].
Andre, I ;
Gonzalez, A ;
Wang, B ;
Katz, J ;
Benoist, C ;
Mathis, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (06) :2260-2263
[2]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[3]   Association between alpha beta TCR(+)CD4(-)CD8(-) T-cell deficiency and IDDM in NOD/Lt mice [J].
Baxter, AG ;
Kinder, SJ ;
Hammond, KJL ;
Scollay, R ;
Godfrey, DI .
DIABETES, 1997, 46 (04) :572-582
[4]   Mouse CD1-specific NK1 T cells: Development, specificity, and function [J].
Bendelac, A ;
Rivera, MN ;
Park, SH ;
Roark, JH .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :535-562
[5]   Regulation of interleukin (IL)-12 receptor β2 subunit expression by endogenous IL-12:: A critical step in the differentiation of pathogenic autoreactive T cells [J].
Chang, JT ;
Shevach, EM ;
Segal, BM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (06) :969-978
[6]   PREVENTION OF DIABETES IN NONOBESE DIABETIC MICE BY DENDRITIC CELL TRANSFER [J].
CLARESALZLER, MJ ;
BROOKS, J ;
CHAI, A ;
VANHERLE, K ;
ANDERSON, C .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) :741-748
[7]   Requirement for V(alpha)14 NKT cells in IL-12-mediated rejection of tumors [J].
Cui, JQ ;
Shin, T ;
Kawano, T ;
Sato, H ;
Kondo, E ;
Toura, I ;
Kaneko, Y ;
Koseki, H ;
Kanno, M ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1623-1626
[8]   CD8+ but not CD8- dendritic cells cross-prime cytotoxic T cells in vivo [J].
den Haan, JMM ;
Lehar, SM ;
Bevan, MJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (12) :1685-1695
[9]   A role for CD4(+)NK1.1(+)T T lymphocytes as major histocompatibility complex class II independent helper cells in the generation of CD8(+) effector function against intracellular infection [J].
Denkers, EY ;
SchartonKersten, T ;
Barbieri, S ;
Caspar, P ;
Sher, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (01) :131-139
[10]  
ESOUSA CR, 1999, IMMUNITY, V11, P637