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由小鼠淋巴细胞激活培养的内皮细胞所导致的实验性自身免疫性血管炎。

Experimental autoimmune type of vasculitis resulting from activation of mouse lymphocytes to cultured endothelium.

作者信息

Hart M N, Sadewasser K L, Cancilla P A, DeBault L E

出版信息

Lab Invest. 1983 Apr;48(4):419-27.

PMID:6834786
Abstract

BALB/c splenic lymphocytes were activated by co-culturing in vitro and in vivo with an endothelial cell line derived from outbred mouse brain capillaries. The lymphocytes underwent proliferation, and after intravenous injection into syngeneic mice, vasculitis was found in lungs, brain, and other organs between 3 and 8 days postinjection. Controls consisted of normal lymphocytes, lymphocytes activated by phytohemaglutinin in vitro, and lymphocytes activated in vivo by cultured fibroblasts or Freund's complete adjuvant. The control lymphocytes did not cause vasculitis when injected into syngeneic mice. Lymphocytes activated by endothelium displayed nonspecific cytotoxicity by 51Cr release against both endothelial and fibroblast cell lines.

摘要

通过体外和体内与源自远交系小鼠脑毛细血管的内皮细胞系共培养,激活BALB/c脾淋巴细胞。淋巴细胞发生增殖,静脉注射到同基因小鼠体内后,在注射后3至8天,在肺、脑和其他器官中发现血管炎。对照组包括正常淋巴细胞、体外被植物血凝素激活的淋巴细胞,以及体内被培养的成纤维细胞或弗氏完全佐剂激活的淋巴细胞。将对照淋巴细胞注射到同基因小鼠体内时不会引起血管炎。被内皮细胞激活的淋巴细胞通过51Cr释放对内皮细胞系和成纤维细胞系均表现出非特异性细胞毒性。

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