High‐affinity immunoglobulin E receptor (FcεRI)‐bearing eosinophils, mast cells, macrophages and Langerhans’ cells in allergen‐induced late‐phase cutaneous reactions in atopic subjects
High‐affinity immunoglobulin E receptor (FcεRI)‐bearing eosinophils, mast cells, macrophages and Langerhans’ cells in allergen‐induced late‐phase cutaneous reactions in atopic subjects
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特应性受试者过敏原诱导的晚期皮肤反应中携带高亲和力免疫球蛋白 E 受体 (FcεRI) 的嗜酸性粒细胞、肥大细胞、巨噬细胞和朗格汉斯细胞
DOI:
10.1046/j.1365-2567.1998.00418.x
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发表时间:
1998
期刊:
影响因子:
6.4
通讯作者:
Kay
中科院分区:
文献类型:
--
作者:
Ying;Barata;Meng;Grant;Barkans;Durham;Kay
We have used in situ hybridization (ISH) and immunohistochemistry (IHC) to investigate the kinetics of the expression for FcεRI mRNA (α‐, β‐ and γ‐chains), the α‐chain protein product, as well as the phenotype of the mRNA‐ or protein‐positive cells in allergen‐induced late‐phase skin reactions in atopic subjects. Compared with diluent controls, there were significant increases in the total numbers of mRNA+ cells for the α‐, β‐and γ‐chains for FcεRI at all time‐points (6, 24 and 48 hr) after allergen challenge (P<0·01). By double IHC/ISH significant increases in α‐, β‐ and γ‐chain mRNA+ macrophages, eosinophils, mast cells and CD1a+ cells were also observed after allergen challenge (P<0·05). The distribution of FcεRI subunit (α‐, β‐, or γ‐chain) mRNA+ co‐localization was CD68+ macrophages (42–47%), EG2+ eosinophils (33–39%), tryptase+ mast cells (5–11%) and CD1a+ Langerhans’ cells (2–4%). Using single IHC, significant increases in the total number of FcεRI protein+ cells (P<0·01) were observed 24 and 48 hr after allergen challenge. Double IHC showed that the distribution of FcεRI+ cells was tryptase+ mast cells (33%), CD68+ macrophages (36%), EG2+ eosinophils (20%), CD1a+ Langerhans’ cells (4%) and unidentified cells (7%), at the 24‐hr allergen‐challenged sites. These observations suggest that the cutaneous late‐phase reaction in man is associated with up‐regulation of FcεRI on eosinophils, macrophages, mast cells and Langerhans’ cells.
影响因子:
4.4
作者:
P. Weller;T. H. Rand;T. Barrett;A. Elovic;David T. W. Wong;R. Finberg
通讯作者:
P. Weller;T. H. Rand;T. Barrett;A. Elovic;David T. W. Wong;R. Finberg
影响因子:
14.2
作者:
BROIDE, DH;GLEICH, GJ;WASSERMAN, SI
通讯作者:
WASSERMAN, SI