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豚鼠结核菌素敏感性的研究:非结核杆菌滤液注射诱导。

TUBERCULIN HYPERSENSITIVENESS IN NON-TUBERCULOUS GUINEA PIGS INDUCED BY INJECTIONS OF BACILLUS-FREE FILTRATES.

机构信息

Department of Pathology of Washington University Medical School, St. Louis.

出版信息

J Exp Med. 1921 May 31;33(6):751-62. doi: 10.1084/jem.33.6.751.

DOI:10.1084/jem.33.6.751
PMID:19868533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2128300/
Abstract
  1. When a guinea pig with well developed peritoneal tuberculosis is injected intraperitoneally with about 20 cc. of a heavy suspension of a virulent tubercle bacillus (Culture H37) death occurs within 24 hours or the animal becomes extremely toxic. Such a peritoneal tuberculosis develops in about 1 month after 1 cc. of. a very heavy suspension of Culture H37 has been introduced into the abdominal cavity. If the viscid fluid which is contained within the peritoneal cavity is mixed with saline solution and passed through a Berkefeld filter a bacillus-free filtrate is obtained which induces in normal guinea pigs a certain degree of cutaneous hypersensitiveness to tuberculin. 2. The abdominal organs and the parietal peritoneum, to which masses of leucocytes and tubercle bacilli are adherent, when crushed and extracted with saline solution yield a filtrate which likewise induces a cutaneous hypersensitiveness. 3. The cutaneous hypersensitiveness does not appear before the 7th or 8th day after the filtrate injection and is therefore considered to be the result of an active sensitization of the animal.
摘要
  1. 当一只患有严重腹膜结核的豚鼠被腹膜内注射约 20 毫升的高浓度毒力结核分枝杆菌悬浮液(Culture H37)时,它会在 24 小时内死亡,或者变得极度中毒。在腹腔内注射 1 毫升 Culture H37 的高浓度悬浮液后约 1 个月,会出现这种腹膜结核。如果将腹膜腔内的粘性液体与生理盐水混合并通过 Berkefeld 过滤器过滤,则可获得无细菌的滤液,该滤液会在正常豚鼠中引起一定程度的结核菌素皮肤过敏。

  2. 腹腔器官和腹膜壁层,其上附着有大量白细胞和结核分枝杆菌,当被压碎并用生理盐水提取时,可得到同样能引起皮肤过敏的滤液。

  3. 皮肤过敏反应在滤液注射后第 7 或第 8 天之前不会出现,因此被认为是动物主动致敏的结果。

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TUBERCULIN HYPERSENSITIVENESS IN NON-TUBERCULOUS GUINEA PIGS INDUCED BY INJECTIONS OF BACILLUS-FREE FILTRATES.豚鼠结核菌素敏感性的研究:非结核杆菌滤液注射诱导。
J Exp Med. 1921 May 31;33(6):751-62. doi: 10.1084/jem.33.6.751.
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J Exp Med. 1950 Feb;91(2):197-218, pl. doi: 10.1084/jem.91.2.197.
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J Exp Med. 1932 Jan 1;55(1):31-54. doi: 10.1084/jem.55.1.31.

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