Skin-resident murine dendritic cell subsets promote distinct and opposing antigen-specific T helper cell responses.
Skin-resident murine dendritic cell subsets promote distinct and opposing antigen-specific T helper cell responses.
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居住的皮肤鼠树突状细胞亚群可促进明显的和相反的抗原特异性T辅助细胞反应。
DOI:
10.1016/j.immuni.2011.06.005
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发表时间:
2011-08-26
期刊:
影响因子:
32.4
通讯作者:
Kaplan DH
中科院分区:
文献类型:
--
作者:
Igyártó BZ;Haley K;Ortner D;Bobr A;Gerami-Nejad M;Edelson BT;Zurawski SM;Malissen B;Zurawski G;Berman J;Kaplan DH
Skin-resident dendritic cells (DC) are well positioned to encounter cutaneous pathogens and are required for the initiation of adaptive immune responses. There are at least 3 subsets of skin DC — Langerhans cells (LC), Langerin+ dermal DC (dDC), and classic dDC. Whether these subsets have distinct or redundant function in vivo is poorly understood. Using a Candida albicans skin infection model, we have shown that direct presentation of antigen by LC is necessary and sufficient for the generation of antigen-specific T helper-17 (Th17) cells but not for the generation of cytotoxic lymphocytes (CTL). In contrast, Langerin+ dDC are required for the generation of antigen specific CTL and Th1 cells. Langerin+ dDC also inhibited the ability of LC and classic DC to promote Th17 responses. This work demonstrates that skin-resident DC subsets promote distinct and opposing antigen-specific responses.
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DOI:
10.1038/jid.2009.343
发表时间:
2010-03
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
通讯作者:
--
DOI:
10.1084/jem.20071966
发表时间:
2007-12-24
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Bursch LS;Wang L;Igyarto B;Kissenpfennig A;Malissen B;Kaplan DH;Hogquist KA
通讯作者:
Hogquist KA
DOI:
10.4049/jimmunol.1001802
发表时间:
2010-10-15
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Bobr A;Olvera-Gomez I;Igyarto BZ;Haley KM;Hogquist KA;Kaplan DH
通讯作者:
Kaplan DH
影响因子:
30.5
作者:
Bedoui, Sammy;Whitney, Paul G.;Heath, William R.
通讯作者:
Heath, William R.
影响因子:
5.4
作者:
Aliahmadi, Ehsan;Gramlich, Robert;Peiser, Matthias
通讯作者:
Peiser, Matthias