CD1d-Restricted Type II NKT Cells Reactive With Endogenous Hydrophobic Peptides.
CD1d-Restricted Type II NKT Cells Reactive With Endogenous Hydrophobic Peptides.
复制标题
DOI:
10.3389/fimmu.2018.00548
复制
发表时间:
2018
影响因子:
7.3
通讯作者:
Ishizu A
中科院分区:
文献类型:
--
作者:
Nishioka Y;Masuda S;Tomaru U;Ishizu A
NKT cells belong to a distinct subset of T cells that recognize hydrophobic antigens presented by major histocompatibility complex class I-like molecules, such as CD1d. Because NKT cells stimulated by antigens can activate or suppress other immunocompetent cells through an immediate production of a large amount of cytokines, they are regarded as immunological modulators. CD1d-restricted NKT cells are classified into two subsets, namely, type I and type II. CD1d-restricted type I NKT cells express invariant T cell receptors (TCRs) and react with lipid antigens, including the marine sponge-derived glycolipid α-galactosylceramide. On the contrary, CD1d-restricted type II NKT cells recognize a wide variety of antigens, including glycolipids, phospholipids, and hydrophobic peptides, by their diverse TCRs. In this review, we focus particularly on CD1d-restricted type II NKT cells that recognize endogenous hydrophobic peptides presented by CD1d. Previous studies have demonstrated that CD1d-restricted type I NKT cells usually act as pro-inflammatory cells but sometimes behave as anti-inflammatory cells. It has been also demonstrated that CD1d-restricted type II NKT cells play opposite roles to CD1d-restricted type I NKT cells; thus, they function as anti-inflammatory or pro-inflammatory cells depending on the situation. In line with this, CD1d-restricted type II NKT cells that recognize type II collagen peptide have been demonstrated to act as anti-inflammatory cells in diverse inflammation-induction models in mice, whereas pro-inflammatory CD1d-restricted type II NKT cells reactive with sterol carrier protein 2 peptide have been demonstrated to be involved in the development of small vessel vasculitis in rats.
登录
查看更多内容
影响因子:
4.4
作者:
Griseri, T;Beaudoin, L;Lehuen, AS
通讯作者:
Lehuen, AS
影响因子:
56.9
作者:
CASTANO, AR;TANGRI, S;PETERSON, PA
通讯作者:
PETERSON, PA
影响因子:
15.9
作者:
Halder, Ramesh C.;Aguilera, Carlos;Kumar, Vipin
通讯作者:
Kumar, Vipin
影响因子:
15.3
作者:
Jahng, A;Maricic, I;Aguilera, C;Cardell, S;Halder, RC;Kumar, V
通讯作者:
Kumar, V
DOI:
10.4049/jimmunol.1601399
发表时间:
2017-02-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Dhodapkar MV;Kumar V
通讯作者:
Kumar V