Immune cell migration in inflammation: present and future therapeutic targets

被引:977
作者
Luster, AD [1 ]
Alon, R
von Andrian, UH
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp,Ctr Immunol & Inflammatory, Dept Med,Div Rheumatol Allergy & Immunol, Boston, MA 02114 USA
[2] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[3] Harvard Univ, Sch Med, CBR Inst Biomed Res, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
基金
美国国家卫生研究院; 以色列科学基金会;
关键词
D O I
10.1038/ni1275
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The burgeoning field of leukocyte trafficking has created new and exciting opportunities in the clinic. Trafficking signals are being defined that finely control the movement of distinct subsets of immune cells into and out of specific tissues. Because the accumulation of leukocytes in tissues contributes to a wide variety of diseases, these 'molecular codes' have provided new targets for inhibiting tissue-specific inflammation, which have been confirmed in the clinic. However, immune cell migration is also critically important for the delivery of protective immune responses to tissues. Thus, the challenge for the future will be to identify the trafficking molecules that will most specifically inhibit the key subsets of cells that drive disease processes without affecting the migration and function of leukocytes required for protective immunity.
引用
收藏
页码:1182 / 1190
页数:9
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