1Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Department of Internal Medicine, Family Medicine and History of Medicine, Osijek, Croatia; 2Čakovec County Hospital, Čakovec, Croatia; 3Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia; 4Rudjer Bošković Institute, Division of Molecular Medicine, Zagreb, Croatia; 5Rudjer Bošković Institute, Division of Molecular Biology, Zagreb, Croatia; 6Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Department of Department of Gynecology and Obstetrics, Osijek, Croatia; 7Dr Andrija Štampar Teaching Institute of Public Health, Zagreb, Croatia.
Acta Clin Croat. 2020 Jun;59(2):351-358. doi: 10.20471/acc.2020.59.02.20.
The role of T regulatory lymphocytes (T) particularly in cancer is well known. The goal of the present study was to determine the contribution of these lymphocytes in the regulation of anti-tumor immunity of CBA/HZgr mice against MC-2 fibrosarcoma (4 generation of methylcholanthrene induced tumor). The levels of T lymphocytes (CD4+, CD8+ and CD4+CD25+) were determined 8 and 20 days after tumor transplantation. Further, the role of CD4+CD25+ (T) in tumor-host interaction was evaluated and by using specific monoclonal antibodies. We found that splenocytes of both control and T depleted tumor bearing mice strongly but differently inhibited growth of tumor cells . While splenocytes of untreated mice exhibited significant decrease of this activity (from 74.4% to 62.6% and 32.95%), the splenocytes of T depleted mice showed increase of this activity (from 79.5% to 84.3% and 86.2%) from day 6 to day 13 and day 21 after tumor grafting, respectively. Further, upon i.v. injecting specific monoclonal anti-T antibody tumor immediately prior to tumor cell intracutaneous transplantation, the tumor was rejected after initial growth. In treated mice, the incidence of T cells was very low initially, reaching normal values two weeks later. These animals were shown to be resistant to tumor transplantation four months later.
调节性 T 淋巴细胞(Treg)在癌症中的作用是众所周知的。本研究的目的是确定这些淋巴细胞在调节 CBA/HZgr 小鼠对 MC-2 纤维肉瘤(4 代甲基胆蒽诱导的肿瘤)抗肿瘤免疫中的作用。在肿瘤移植后 8 天和 20 天测定 T 淋巴细胞(CD4+、CD8+和 CD4+CD25+)的水平。进一步,通过使用特异性单克隆抗体评估 CD4+CD25+(Treg)在肿瘤-宿主相互作用中的作用。我们发现,荷瘤小鼠的脾细胞强烈但不同地抑制肿瘤细胞的生长。而未处理的小鼠的脾细胞显示出这种活性的显著降低(从 74.4%降至 62.6%和 32.95%),而 T 细胞耗竭的小鼠的脾细胞显示出这种活性的增加(从 79.5%增加到 84.3%和 86.2%),分别从肿瘤接种后第 6 天、第 13 天和第 21 天。此外,在肿瘤细胞皮内移植前静脉内注射特异性单克隆抗 T 抗体,肿瘤在最初生长后被排斥。在治疗小鼠中,T 细胞的发生率最初非常低,两周后恢复正常。这些动物在四个月后对肿瘤移植具有抗性。