Baird S M, Beattie G M, Lannom R A, Lipsick J S, Jensen F C, Kaplan N O
Cancer Res. 1982 Jan;42(1):198-206.
Athymic mice infected with pinworms or carrying human tumor xenografts frequently develop a lymphoproliferative disorder which eventually leads to lymphoma. By immunofluorescent analysis of involved tissues, the lymphomas appear to be mixtures of null cells, B-cells, and T-cells. When each lymphoma is established in tissue culture, a predominant cell type grows out. We have now established lymphoma lines of null cells, B-cells, and T-cells. Lymphoma development is preceded by the secretion into the bloodstream of large amounts of murine leukemia virus M.W. 70,000 glycoprotein antigen; however, very little virus is produced. In vivo, the expression of viral envelope antigen appears within a few days after human tumor transplantation and precedes the development of lymphoma by about a month. Cells expressing viral antigens are first seen in the diffuse cortex of lymph nodes and the periarteriolar white sheath of the spleen, the tissue domains in which lymphomas also first appear.
感染蛲虫或携带人肿瘤异种移植物的无胸腺小鼠经常会发生淋巴细胞增生性疾病,最终导致淋巴瘤。通过对受累组织的免疫荧光分析,淋巴瘤似乎是裸细胞、B细胞和T细胞的混合物。当每个淋巴瘤在组织培养中建立时,一种主要的细胞类型会生长出来。我们现在已经建立了裸细胞、B细胞和T细胞的淋巴瘤系。淋巴瘤的发展之前,大量分子量为70,000的鼠白血病病毒糖蛋白抗原会分泌到血液中;然而,产生的病毒很少。在体内,病毒包膜抗原的表达在人肿瘤移植后几天内出现,比淋巴瘤的发展提前约一个月。表达病毒抗原的细胞首先出现在淋巴结的弥漫皮质和脾脏的动脉周围白鞘中,淋巴瘤也首先出现在这些组织区域。