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卡介苗致敏小鼠体内艾氏腹水癌的消退

Regression of Ehrlich ascites carcinoma in BCG-sensitized mice.

作者信息

Turcotte R

出版信息

Rev Can Biol. 1977 Sep;36(3):253-63.

PMID:928853
Abstract

Intraperitoneal inoculation of CF1 mice with Bacillus Calmette-Guérin (BCG) protected many of them against the ascites form of Ehrlich carcinoma; and, for those that developed cancer, complete regression occurred in up to 50% of the cases at an advanced state of the neoplastic disease. In contrast, when a booster dose of BCG was administered in admixture with tumor cells, the incidence of the tumor was lower and tumor regressions were very rarely observed in mice that developed cancer. Trypan blue, an inhibitor of lysosomal enzymes of macrophages, was found to markedly suppress the natural (innate) antitumor resistance of control mice as well as the acquired resistance and tumor regressions of BCG-sensitized mice. Moreover, a comparison of the cytotoxic activity of the adherent (macrophages) and nonadherent (predominantly lymphocytes) cells isolated from the peritoneal cavity of BCG-sensitized mice, as measured by the inhibition of DNA synthesis, revealed that the effector cells were amongst the macrophages. In contrast, spleen macrophages were devoid of cytotoxicity. The spleen lymphocytes from both BCG-sensitized and control mice possessed about the same significant cytotoxic activity. These results indicate that the activated peritoneal macrophages, induced by a local injection of BCG, could play an important role in the antitumor immunity against Ehrlich carcinoma.

摘要

给CF1小鼠腹腔接种卡介苗(BCG)可保护许多小鼠免受艾氏腹水癌腹水型的侵害;对于那些患上癌症的小鼠,在肿瘤疾病晚期,高达50%的病例出现了完全消退。相比之下,当将一剂加强剂量的卡介苗与肿瘤细胞混合注射时,肿瘤发生率较低,且在患上癌症的小鼠中很少观察到肿瘤消退。台盼蓝是巨噬细胞溶酶体酶的抑制剂,发现它能显著抑制对照小鼠的天然(固有)抗肿瘤抵抗力以及卡介苗致敏小鼠的获得性抵抗力和肿瘤消退。此外,通过测量DNA合成抑制来比较从卡介苗致敏小鼠腹腔分离出的贴壁细胞(巨噬细胞)和非贴壁细胞(主要是淋巴细胞)的细胞毒性活性,发现效应细胞存在于巨噬细胞之中。相比之下,脾巨噬细胞没有细胞毒性。卡介苗致敏小鼠和对照小鼠的脾淋巴细胞具有大致相同的显著细胞毒性活性。这些结果表明,局部注射卡介苗诱导的活化腹腔巨噬细胞在针对艾氏癌的抗肿瘤免疫中可能发挥重要作用。

相似文献

1
Regression of Ehrlich ascites carcinoma in BCG-sensitized mice.卡介苗致敏小鼠体内艾氏腹水癌的消退
Rev Can Biol. 1977 Sep;36(3):253-63.
2
A comparison of in vitro cell-mediated reactivity against syngeneic tumor cells by various lymphoid cell populations from Bacillus Calmette-Guérin-tumor-cured, tumor-sensitized, tumor-bearing, and normal inbred guinea pigs.对来自卡介苗-肿瘤治愈、肿瘤致敏、荷瘤和正常近交系豚鼠的各种淋巴细胞群体针对同基因肿瘤细胞的体外细胞介导反应性进行比较。
Cancer Res. 1976 Dec;36(12):4459-66.
3
Lymphocyte-macrophage interactions in BCG-treated mice.卡介苗处理小鼠中淋巴细胞与巨噬细胞的相互作用
Recent Results Cancer Res. 1976(56):49-57. doi: 10.1007/978-3-642-81049-7_7.
4
The role of the BCG dose and the mouse strain in the inhibition of development of neoplasms susceptible and nonsusceptible to the action of natural cytotoxic cells.卡介苗剂量和小鼠品系在抑制对自然细胞毒性细胞作用敏感和不敏感的肿瘤发生中的作用。
Folia Histochem Cytobiol. 1985;23(1-2):3-10.
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Effect of nonspecific immune stimulation with BCG and polidin on the Ehrlich ascites tumor growth.卡介苗和聚维酮碘非特异性免疫刺激对艾氏腹水瘤生长的影响。
Morphol Embryol (Bucur). 1985 Jul-Sep;31(3):217-25.
6
Analysis of the immunologic mechanism of intravesical bacillus Calmette-Guerin therapy for superficial bladder tumors: distribution and function of immune cells.卡介苗膀胱灌注治疗浅表性膀胱肿瘤的免疫机制分析:免疫细胞的分布与功能
J Korean Med Sci. 1993 Apr;8(2):135-44. doi: 10.3346/jkms.1993.8.2.135.
7
Nonspecific cytotoxicity of vaccinia-induced peritoneal exudates in hamsters is mediated by Thy-1.2 homologue-positive cells distinct from NK cells and macrophages.痘苗诱导的仓鼠腹腔渗出液的非特异性细胞毒性由不同于自然杀伤细胞和巨噬细胞的Thy-1.2同源阳性细胞介导。
J Immunol. 1983 Nov;131(5):2545-50.
8
Antitumor effect of lymphocyte and macrophage from mice immunized with Ehrlich ascites tumor cells.用艾氏腹水瘤细胞免疫的小鼠的淋巴细胞和巨噬细胞的抗肿瘤作用。
Mie Med J. 1971 Jan;20(3):227-41.
9
Macrophage activation for tumor cytotoxicity: induction of tumoricidal macrophages by supernatants of PPD-stimulated Bacillus Calmette-Guérin-immune spleen cell cultures.巨噬细胞激活以实现肿瘤细胞毒性:通过卡介苗刺激的卡介苗免疫脾细胞培养上清液诱导杀肿瘤巨噬细胞。
J Immunol. 1977 Sep;119(3):889-96.
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Tumour resistance of mice infected with salmonella enteritidis 11RX. The role of peritoneal exudate cells.感染肠炎沙门氏菌11RX的小鼠的肿瘤抗性。腹腔渗出细胞的作用。
Aust J Exp Biol Med Sci. 1973 Dec;51(6):801-9. doi: 10.1038/icb.1973.76.