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含转移因子活性的可透析白细胞提取物作用的体外测定

In vitro determination of effects of dialyzable leukocyte extracts containing transfer factor activity.

作者信息

Schroder I, Rovensky J

出版信息

Allergol Immunopathol (Madr). 1982 May-Jun;10(3):171-6.

PMID:7148610
Abstract

The studies for determining the effects of dialyzable leukocyte extracts (transfer factor) as reflected in recovery of E-rosetting capacity in trypsinised lymphocytes (recovery-assay) suggested the following: 1. Dialyzable leukocyte extracts contain an inhibitor with a molecular weight of about 5000 (fraction I). 2. This inhibitor considerably affects the immunologic activity of both whole preparations and their different fractions during the in vitro activity assay. 3. The inhibitor fraction that fails to respond to the "recovery-assay" (less than 5%) responds very actively to the test after inactivation (45 min/57 degrees C). 4. Therefore, activation assays performed on the total preparation after inactivation involve a considerable error. 5. Immunological activity is concentrated in fractions III and IV. Only fraction III activity can be reduced considerably by inactivation. Fraction II activity is induced by incomplete separation from fraction III. Fraction IV cannot be inactivated. 6. In the case of transfer factor preparations (without inhibitor fractions) activity increases almost in direct proportion to the concentration up to about 30 micrograms. 7. Since the "recovery-assay" also responds to substances with no immunologic activity, its use can be justified in the case of fraction III. The activity is then the difference between the native and the inactivated forms. 8. A corresponding review of methods (such as LTT, migration inhibition test, skin test, etc.) currently used for activity assays seems advisable.

摘要

关于测定可透析白细胞提取物(转移因子)对胰蛋白酶处理的淋巴细胞中E-玫瑰花结形成能力恢复情况(恢复试验)影响的研究表明如下:1. 可透析白细胞提取物含有一种分子量约为5000的抑制剂(组分I)。2. 该抑制剂在体外活性测定过程中对整个制剂及其不同组分的免疫活性有相当大的影响。3. 对“恢复试验”无反应的抑制剂组分(小于5%)在灭活后(45分钟/57摄氏度)对试验反应非常活跃。4. 因此,对灭活后的总制剂进行的活化试验存在相当大的误差。5. 免疫活性集中在组分III和IV中。只有组分III的活性可通过灭活而大幅降低。组分II的活性是由于与组分III分离不完全而诱导产生的。组分IV不能被灭活。6. 对于转移因子制剂(不含抑制剂组分),活性几乎与浓度成正比增加,直至约30微克。7. 由于“恢复试验”也对无免疫活性的物质有反应,因此在组分III的情况下使用该试验是合理的。此时活性是天然形式和灭活形式之间的差异。8. 对目前用于活性测定的方法(如淋巴细胞转化试验、迁移抑制试验、皮肤试验等)进行相应的综述似乎是可取的。

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