TIM-1 and TIM-3 enhancement of Th2 cytokine poduction by mast cells

被引:146
作者
Nakae, Susumu
Iikura, Motoyasu
Suto, Hajime
Akiba, Hisaya
Umetsu, Dale T.
DeKruyff, Rosemarie H.
Saito, Hirohisa
Galli, Stephen J.
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Natl Res Inst Child Hlth & Dev, Dept Allergy & Immunol, Tokyo, Japan
[3] Juntendo Univ, Atopy Res Ctr, Tokyo, Japan
[4] Juntendo Univ, Dept Immunol, Tokyo, Japan
[5] Harvard Univ, Sch Med, Childrens Hosp Boston, Div Immunol, Boston, MA USA
关键词
D O I
10.1182/blood-2006-11-058800
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Members of the T-cell immunoglobullin and mucin-domain-containing molecule (TIM) family have roles in T-cell-mediated immune responses. TIM-1 and TIM-2 are predominantly expressed on T helper type 2 (Th2) cells, whereas TIM-3 is preferentially expressed on Th1 and Th17 cells. We found that TIM-1 and TIM-3, but neither TIM-2 nor TIM-4, were constitutively expressed on mouse peritoneal mast cells and bone marrow-derived cultured mast cells (BMCMCs). After IgE + Ag stimulation, TIM-1 expression was down-regulated on BMCMCs, whereas TIM-3 expression was up-regulated. We also found that recombinant mouse TIM-4 (rmTIM-4), which is a ligand for TIM-1, as well as an anti-TIM-3 polyclonal Ab, can promote interleukin-4 (IL-4), IL-6, and IL-13 production without enhancing degranulation in BMCMCs stimulated with IgE + Ag. More-over, the anti-TIM-3 Ab, but neither anti-TIM-1 Ab nor rmTIM-4, suppressed mast-cell apoptosis. These observations suggest that TIM-1 and TIM-3 may be able to influence T-cell-mediated immune responses in part through effects on mast cells.
引用
收藏
页码:2565 / 2568
页数:4
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