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[使用皮肤试验和放射性变应原吸附抑制试验评估过敏原制剂豚草的效力]

[Evaluation of the potency of the allergen preparation Ambrosia elatior using a skin test and the inhibition radioallergosorbent test].

作者信息

Stipić-Marković A, Sket-Janković N, Cvoriscec B

机构信息

Odjel za klinicku imunologiju i pulmologiju, Opće bolnice Sv. Duh, Zagreb.

出版信息

Lijec Vjesn. 1992 Jan-Apr;114(1-4):53-6.

PMID:1343028
Abstract

The total allergenicity of a pollen extract Ambrosia elatior was measured by quantitative prick test applied to the skin of seven highly sensitive patients and by standardized method of RAST-inhibition. Five 10-fold dilutions of the allergen concentration together with histamine hydrochloride 1 mg/ml (H1) were used. The induced wheal diametres for each concentration in per cent of the patient's own histamine wheal, were calculated. There was highly significant correlation (r = 0.9951) between the intensity of IgE mediated skin reactions and the IgE binding molecules in whole pollen extract. The concentration which provides the wheal equivalent to those of H1, found by linear regression analyses, was 54.9 micrograms/ml) in order to inhibit radioallergosorbent test with a pooled serum from the same patients, containing specific IgE antibodies against relevant allergens. Relevant allergen was a disk-allergen W1 (Pharmacia Diagnostics, Uppsala) The quantity of inhibition was proportional with allergen concentration (r = 0.9813). The concentration of 55.9 micrograms/ml, by linear regression analyses elicits inhibition of 50 per cent in RAST. It is concluded that quantitative prick test and histamine estimated skin sensitivity have a good clinical applicability in assessment of releaseability of skin mast cells, and together with RAST inhibition, provides the precise combined method for calibration of an allergenic extract potency.

摘要

通过对7名高敏患者皮肤进行定量点刺试验以及采用标准化的放射性变应原吸附试验(RAST)抑制法,测定了豚草花粉提取物的总变应原性。使用了变应原浓度的5种10倍稀释液以及1mg/ml的盐酸组胺(H1)。计算每种浓度下诱发的风团直径相对于患者自身组胺风团的百分比。IgE介导的皮肤反应强度与全花粉提取物中的IgE结合分子之间存在高度显著的相关性(r = 0.9951)。通过线性回归分析发现,产生与H1相同风团的浓度为54.9微克/毫升,该浓度可抑制来自相同患者的含有针对相关变应原的特异性IgE抗体的混合血清的放射性变应原吸附试验。相关变应原为盘状变应原W1(Pharmacia Diagnostics,乌普萨拉)。抑制量与变应原浓度成正比(r = 0.9813)。通过线性回归分析,55.9微克/毫升的浓度在RAST中可引起50%的抑制。结论是,定量点刺试验和组胺评估的皮肤敏感性在评估皮肤肥大细胞的释放能力方面具有良好的临床适用性,并且与RAST抑制一起,为校准变应原提取物效力提供了精确的联合方法。

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