Immune characterization of an individual with an exceptionally high natural killer T cell frequency and her immediate family

被引:23
作者
Chan, A. C. [1 ]
Serwecinska, L. [1 ]
Cochrane, A. [3 ]
Harrison, L. C. [2 ]
Godfrey, D. I. [1 ]
Berzins, S. P. [1 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
[2] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
[3] Royal Childrens Hosp, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
autoimmunity; NKT; T cell; type; 1; diabetes; CD1D-RESTRICTED NKT CELLS; GLYCOLIPID ANTIGENS; CYTOKINE PRODUCTION; AUTOIMMUNE-DISEASE; DISTINCT SUBSETS; PHASE-I; EXPANSION; THYMUS; CANCER; GLYCOSPHINGOLIPIDS;
D O I
10.1111/j.1365-2249.2009.03888.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Natural killer T cells (NKT) are a regulatory subset of T lymphocytes whose frequency in peripheral blood is highly variable within the human population. Lower than normal NKT frequencies are associated with increased predisposition to a number of diseases, including type 1 diabetes and some forms of cancer, raising the possibility that an increased frequency may be protective. However, there is little or no understanding of how high NKT frequencies arise or, most importantly, whether the potential exists to boost and maintain NKT levels for therapeutic advantage. Here, we provide a detailed functional and phenotypic characterization of the NKT compartment of a human donor with NKT levels approximately 50 times greater than normal, including an analysis of NKT in her immediate family members. The study focuses upon the characteristics of this donor and her family, but demonstrates more broadly that the size and flexibility of the NKT niche is far greater than envisioned previously. This has important implications for understanding how the human NKT compartment is regulated, and supports the concept that the human NKT compartment might be expanded successfully for therapeutic benefit.
引用
收藏
页码:238 / 245
页数:8
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