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A组链球菌C多糖复合物所致结缔组织实验性损伤的分析。I. 组织与毒素的体内反应。

Analysis of the experimental lesion of connective tissue produced by a complex of C polysaccharide from group A streptococci. I. In vivo reaction between tissue and toxin.

作者信息

SCHWAB J H

出版信息

J Exp Med. 1962 Jul 1;116(1):17-28. doi: 10.1084/jem.116.1.17.

Abstract

Specific antibody and a glucosaminidase enzyme react with the serologically active sites on C polysaccharide, and local injection of these reagents will neutralize the toxic effect of C polysaccharide complexes even after an interval of 24 to 72 hours. The cell wall lysins in S. albus filtrate and from phage-lysed Group C streptococci, break down the cell wall structure of Group A streptococci but leave the serological reactive sites of the C polysaccharide intact. These reagents lose much of their ability to neutralize the C polysaccharide toxin when superinjected after an interval of 4 hours following toxin injections. Toxic C polysaccharide cannot be recovered from an injection site by intercellular perfusion of the excised skin area after an interval of 1 to 4 hours following toxin injection. It is concluded that toxic particles of C polysaccharide complexes combine firmly with the dermal tissue of rabbits within 1 to 4 hours following intracutaneous injection. The cell wall lysins neutralize the toxin by reducing the particle size of C polysaccharide complexes. This minimum particle size is required for the initial reaction with tissue and when this has occurred these reagents are no longer able to influence the development of the lesion.

摘要

特异性抗体和一种葡糖胺酶与C多糖的血清学活性位点发生反应,即使在间隔24至72小时后,局部注射这些试剂也会中和C多糖复合物的毒性作用。白色链霉菌滤液和噬菌体裂解的C组链球菌中的细胞壁溶解素会破坏A组链球菌的细胞壁结构,但C多糖的血清学反应位点保持完整。在毒素注射后间隔4小时再注射这些试剂时,它们中和C多糖毒素的能力会大大降低。在毒素注射后1至4小时的间隔时间后,通过对切除的皮肤区域进行细胞间灌注,无法从注射部位回收有毒的C多糖。结论是,C多糖复合物的有毒颗粒在皮内注射后1至4小时内与兔的真皮组织牢固结合。细胞壁溶解素通过减小C多糖复合物的颗粒大小来中和毒素。这种最小颗粒大小是与组织发生初始反应所必需的,一旦发生这种情况,这些试剂就不再能够影响病变的发展。

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