Repeated α-galactosylceramide administration results in expansion of NK T cells and alleviates inflammatory dermatisis in MRL-lpr/lpr mice

被引:98
作者
Yang, JQ
Saxena, V
Xu, HL
Van Kaer, L
Wang, CR
Singh, RR
机构
[1] Univ Cincinnati, Dept Internal Med, Autoimmun & Tolerance Lab, Cincinnati, OH 45267 USA
[2] Univ Chicago, Gwen Knapp Ctr, Chicago, IL 60637 USA
[3] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN 37232 USA
关键词
D O I
10.4049/jimmunol.171.8.4439
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK T (NKT) cells expressing the invariant Valpha14-Jalpha18 TCR alpha-chain recognize glycolipid Ags such as a-galactosylceramide (alpha-GalCer) presented by the NIHC class I-like molecule CD1d. Upon activation by alpha-GalCer, invariant NKT cells secrete multiple cytokines and confer protection in certain immune-mediated disorders. Here we have investigated the role of NKT cells in the development of inflammatory dermatitis; in MRL-lpr/lpr mice, which shares features with lupus; in humans. Our results show that the numbers and functions of NKT (TCRbeta(+)CD1d/alpha-GalCer tetramer(+)) cells, particularly of the NK1.1(-) subset, are reduced in MRL-lpr/lpr mice compared with MRL-fas/fas and/or nonautoimmune C3H/Hej and BALB/c mice. Repeated treatments with alpha-GalCer result in the expansion of NKT cells and alleviate dermatitis in MRL-lpr/lpr mice. Our results indicate that NKT cell deficiency can be corrected by repeated alpha-GalCer treatment and that NKT cells may play a protective role in inflammatory dermatitis of lupus-prone mice.
引用
收藏
页码:4439 / 4446
页数:8
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