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链格孢属过敏原研究。I. 用于测定链格孢属过敏原的放射变应原吸附试验的建立。

Studies on Alternaria allergens. I. Establishment of the radioallergosorbent test for measurement of Alternaria allergens.

作者信息

Yunginger J W, Roberts G D, Gleich G J

出版信息

J Allergy Clin Immunol. 1976 Apr;57(4):293-301. doi: 10.1016/0091-6749(76)90085-3.

DOI:10.1016/0091-6749(76)90085-3
PMID:944203
Abstract

The ability to covalently couple Alternaria allergens to microcrystalline cellulose particles has permitted not only the measurement of IgE antibodies to Alternaria in patient serums but also the identification of allergenic fractions from crude Alternaria extracts. Crude aqueous Alternaria extracts from 3 commerical suppliers were coupled to cellulose but failed to bind more than 5% of total radioactive counts (TRC) when reacted with serums from highly sensitive patients. Fractionation of a commercial extract through Sephadex G-25 showed that almost all allergenic activity was located in a protein- and carbohydrate-containing peak eluting at the column void volume. These fractions were pooled and coupled to cellulose to yield a RAST polymer which produced up to 20% TRC binding when tested with serums from over 100 Alternaria-sensitive patients, and only up to 1% TRC binding with 17 nonallergic serums. The study of commercial Alternaria extracts by chromatographic and Rast inhibition techniques showed that present extracts are neither qualitatively or quantitatively comparable.

摘要

将链格孢属过敏原与微晶纤维素颗粒进行共价偶联的能力,不仅使得在患者血清中检测针对链格孢属的IgE抗体成为可能,还能从链格孢属粗提物中鉴定出变应原组分。来自3个商业供应商的链格孢属粗水提物与纤维素偶联,但在与高敏患者的血清反应时,结合的总放射性计数(TRC)不超过5%。通过葡聚糖G-25对一种商业提取物进行分级分离显示,几乎所有的变应原活性都位于在柱空体积处洗脱的一个含蛋白质和碳水化合物的峰中。将这些组分合并并与纤维素偶联,得到一种放射性变应原吸附试验(RAST)聚合物,在用100多名对链格孢属过敏患者的血清进行检测时,其产生的TRC结合率高达20%,而与17份非过敏血清反应时,TRC结合率仅高达1%。通过色谱和RAST抑制技术对商业链格孢属提取物进行研究表明,目前的提取物在质量或数量上均无可比性。

相似文献

1
Studies on Alternaria allergens. I. Establishment of the radioallergosorbent test for measurement of Alternaria allergens.链格孢属过敏原研究。I. 用于测定链格孢属过敏原的放射变应原吸附试验的建立。
J Allergy Clin Immunol. 1976 Apr;57(4):293-301. doi: 10.1016/0091-6749(76)90085-3.
2
Allergens of Alternaria: further characterization of a basic allergen fraction.链格孢属变应原:一种碱性变应原组分的进一步特性分析
Int Arch Allergy Appl Immunol. 1983;71(1):83-7. doi: 10.1159/000233366.
3
Immunochemical and physicochemical characterization of commercial Alternaria extracts: a model for standardization of mold allergen extracts.市售链格孢提取物的免疫化学和物理化学特性:霉菌变应原提取物标准化的一个模型
J Allergy Clin Immunol. 1982 Dec;70(6):432-6. doi: 10.1016/0091-6749(82)90005-7.
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Shared allergenic and antigenic determinants in Alternaria and Stemphylium extracts.链格孢属和匍柄霉属提取物中的共同变应原和抗原决定簇。
J Allergy Clin Immunol. 1982 Dec;70(6):437-44. doi: 10.1016/0091-6749(82)90006-9.
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Studies on Alternaria allergens. II. Measurement of the relative potency of commercial Alternaria extracts by the direct RAST and by RAST inhibition.
J Allergy Clin Immunol. 1976 Sep;58(3):405-13. doi: 10.1016/0091-6749(76)90121-4.
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Studies on Alternaria allergens. I. Isolation of allergens from Alternaria tenuis and Alternaria solani.链格孢属过敏原研究。I. 从细交链格孢和番茄链格孢中分离过敏原。
Int Arch Allergy Appl Immunol. 1979;60(3):229-39. doi: 10.1159/000232347.
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Studies on alternaria allergens. II. Presence of two related antigens with contrasting allergenic properties in Alternaria tenius extracts.
Int Arch Allergy Appl Immunol. 1981;65(4):410-6.
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J Allergy Clin Immunol. 1980 Aug;66(2):138-47. doi: 10.1016/0091-6749(80)90061-5.
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Studies on alternaria allergens. IV. Comparative biochemical and immunological studies of commercial Alternaria tenuis Batches.交链孢霉过敏原的研究。IV. 商用细交链孢霉批次的比较生化与免疫学研究。
Int Arch Allergy Appl Immunol. 1984;74(3):256-61.
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Antigens of alternaria. I. Isolation and partial characterization of a basic peptide allergen.
J Allergy Clin Immunol. 1983 Mar;71(3):277-82. doi: 10.1016/0091-6749(83)90081-7.

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[Studies on antigenic relationship between grass- and cult. rye pollens by skin-test, RAST and RAST-inhibition-test in patients with pollinosis (author's transl)].[通过皮肤试验、放射变应原吸附试验(RAST)及RAST抑制试验对花粉症患者进行草花粉与栽培黑麦花粉抗原关系的研究(作者译)]
Arch Dermatol Res (1975). 1977 Oct 27;260(1):17-27. doi: 10.1007/BF00558010.