Cutting edge: Leukocyte receptor complex-encoded immunomodulatory receptors show differing specificity for alternative HLA-B27 structures

被引:137
作者
Allen, RL
Raine, T
Haude, A
Trowsdale, J
Wilson, MJ
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] GlaxoSmithKline, Discovery Res, Stevenage, Herts, England
关键词
D O I
10.4049/jimmunol.167.10.5543
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied recognition of the disease-associated HLA-B27 allele by immunomodulatory receptors encoded within the leukocyte receptor complex. BLA class I are ligands for members of the killer Ig receptor (KIR) and Ig-like transcript (ILT)/LER/LILR families (the new LILR nomenclature is described at www. gene.ucl.ac.uk/nomenclature/genefamily/lilr.html). Members of these families bound HLA-B27 in both classical and beta (2) microglobulin-independent forms. Classical complexes bound ILT2, ILT4, and LIR6 transfectants but not ILT1, ILT3, or ILT5. A free H chain form of HLA-B27 bound ILT4 and LIR6. Both forms of HLA-B27 bound KIR3DL1 transfectants. HLA-B27 free H chain bound CD14(+) cells in PBL from healthy controls, consistent with ILT4 expression on monocytes. Alternative recognition of different forms of HLA-B27: by KIR or ILT could influence their immunomodulatory function and may imply a role in inflammatory disease.
引用
收藏
页码:5543 / 5547
页数:5
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