Kay A B, Ying S, Varney V, Gaga M, Durham S R, Moqbel R, Wardlaw A J, Hamid Q
Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, UK.
J Exp Med. 1991 Mar 1;173(3):775-8. doi: 10.1084/jem.173.3.775.
Cryostat sections from skin biopsies from 24-h allergen-induced late-phase cutaneous reactions (LPR) in 14 human atopic subjects were hybridized with 35S-labeled RNA probes for a number of cytokines. mRNA was detected for interleukin 3 (IL-3) (8/14), IL-4 (10/14), IL-5 (11/14), and granulocyte/macrophage colony-stimulating factor (GM-CSF) (13/14). Only 5 of 14 gave hybridization signals for IL-2, and 0 of 14 for interferon gamma. Biopsies from diluent controls gave only occasional weak signals. These results suggest that cells infiltrating the site of the 24-h LPR transcribe mRNA for the IL-3, IL-4, IL-5, and GM-CSF gene cluster and support the hypothesis that atopy is associated with preferential activation of cells having a similar cytokine profile to the murine T helper type 2 subset.
对14名人类特应性受试者在变应原诱导的24小时迟发性皮肤反应(LPR)中获取的皮肤活检组织进行冷冻切片,与多种细胞因子的35S标记RNA探针杂交。检测到白细胞介素3(IL-3)(8/14)、IL-4(10/14)、IL-5(11/14)和粒细胞/巨噬细胞集落刺激因子(GM-CSF)(13/14)的mRNA。14例中只有5例出现IL-2杂交信号,14例中0例出现γ干扰素杂交信号。稀释剂对照的活检组织仅偶尔出现微弱信号。这些结果表明,浸润24小时LPR部位的细胞转录IL-3、IL-4、IL-5和GM-CSF基因簇的mRNA,并支持以下假说:特应性与具有与小鼠2型辅助性T细胞亚群相似细胞因子谱的细胞优先激活有关。