CD1d and invariant NKT cells at the human maternal-fetal interface

被引:142
作者
Boyson, JE
Rybalov, B
Koopman, LA
Exley, M
Balk, SP
Racke, FK
Schatz, F
Masch, R
Wilson, SB
Strominger, JL [1 ]
机构
[1] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[2] Beth Israel Deaconess Med Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Johns Hopkins Univ, Dept Pathol, Baltimore, MD 21287 USA
[5] NYU, Med Ctr, Dept Obstet & Gynecol, New York, NY 10016 USA
[6] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
D O I
10.1073/pnas.162491699
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
Invariant CD1d-restricted natural killer T (iNKT) cells comprise a small, but significant, immunoregulatory T cell subset. Here, the presence of these cells and their CD1d ligand at the human maternal-fetal interface was investigated. Immunohistochemical staining of human decidua revealed the expression of CD1d on both villous and extravillous trophoblasts, the fetal cells that invade the maternal decidua. Decidual iNKT cells comprised 0.48% of the decidual CD3+ T cell population, a frequency 10 times greater than that seen in peripheral blood. Interestingly, decidual CID4+ iNKT cells exhibited a striking Th1-like bias (IFN-gamma production), whereas peripheral blood CD4+ iNKT clones exhibited a Th2-like bias (1L-4 production). Moreover, compared to their peripheral blood counterparts, decidual iNKT clones were strongly polarized toward granulocyte/macrophage colony-stimulating factor production. The demonstration of CD1d expression on fetal trophoblasts together with the differential pattern of cytokine expression by decidual iNKT cells suggests that maternal iNKT cell interactions with CD1d expressed on invading fetal cells may play an immunoregulatory role at the maternal-fetal interface.
引用
收藏
页码:13741 / 13746
页数:6
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