THE ROLE OF REGULATORY T LYMPHOCYTES IN IMMUNE CONTROL OF MC-2 FIBROSARCOMA

The role of T regulatory lymphocytes (T-reg) 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 (4th generation of methylcholanthrene induced tu...

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Veröffentlicht in:Acta clinica Croatica (Tisak) 2020-06, Vol.59 (2), p.351-358
Hauptverfasser: Jukic, Tomislav, Martic, Ana Jurin, Ivankovic, Sinisa, Antica, Mariastefania, Jukic, Doroteja Pavan, Rotim, Cecilija, Jurin, Mislav
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Sprache:eng
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Zusammenfassung:The role of T regulatory lymphocytes (T-reg) 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 (4th 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-regs) in tumor-host interaction was evaluated in vitro and in vivo by using specific monoclonal antibodies. We found that splenocytes of both control and T-reg depleted tumor bearing mice strongly but differently re inhibited growth of tumor cells in vitro. While splenocytes of untreated mice exhibited significant decrease of this activity (from 74.4% to 62.6% and 32.95%), the splenocytes of T-reg 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-reg antibody tumor immediately prior to tumor cell intracutaneous transplantation, the tumor was rejected after initial growth. In treated mice, the incidence of T-reg cells was very low initially, reaching normal values two weeks later. These animals were shown to be resistant to tumor transplantation four months later.
ISSN:0353-9466
1333-9451
DOI:10.20471/acc.2020.59.02.20