Indrová Marie, Bieblová Jana, Rossowska Joana, Kuropka Piotr, Pajtasz-Piasecka Elzbieta, Bubeník Jan, Reinis Milan
Institute of Molecular Genetics, Academy of Sciences of the Czech Republic, v. v. i., 142 20 Prague 4, Czech Republic.
Int J Oncol. 2009 Jan;34(1):173-9.
We have examined the effect of IL-12-producing cellular vaccines on the cytotoxicity and proliferative potential of CD45+ tumour-infiltrating cells (TIL) in mice carrying syngeneic TC-1 and TC-1/A9 HPV 16-associated tumours after chemotherapy with CBM-4A ifosfamide derivative. The chemotherapy resulted in the decrease of the CD4+ and CD8+ TIL, increase of the Gr-1+/CD11b+ TIL, no changes in the infiltration with CD4+/CD25+ Treg TIL, and decrease of the cytolytic and proliferative potential of the CD45+ TIL. Subsequent immunotherapy with the IL-12-producing, genetically modified TC-1 (TC-1-IL-12) cells increased tumour infiltration with CD8+ and CD4+ cells, decreased the Gr-1+/CD11b+ cells, and increased the cytolytic and proliferative potential of the CD45+ TIL. Taken together, these findings suggest that peritumoral administration of the IL-12-producing cellular vaccine can restore the cytolytic potential and inhibit immunosuppressive TIL-dependent mechanisms in the individuals bearing HPV 16-associated tumours, and explain our previously described tumour-inhibitory effects of the vaccine in mice with minimal residual disease after the tumour chemotherapy.
我们研究了在携带同基因TC-1和TC-1/A9人乳头瘤病毒16型相关肿瘤的小鼠中,经CBM-4A异环磷酰胺衍生物化疗后,产生白细胞介素-12的细胞疫苗对CD45+肿瘤浸润细胞(TIL)的细胞毒性和增殖潜力的影响。化疗导致CD4+和CD8+TIL减少,Gr-1+/CD11b+TIL增加,CD4+/CD25+调节性T细胞TIL浸润无变化,以及CD45+TIL的细胞溶解和增殖潜力降低。随后用产生白细胞介素-12的基因改造TC-1(TC-1-IL-12)细胞进行免疫治疗,增加了CD8+和CD4+细胞的肿瘤浸润,减少了Gr-1+/CD11b+细胞,并增加了CD45+TIL的细胞溶解和增殖潜力。综上所述,这些发现表明,在携带人乳头瘤病毒16型相关肿瘤的个体中,瘤周给予产生白细胞介素-12的细胞疫苗可以恢复细胞溶解潜力并抑制依赖免疫抑制TIL的机制,这也解释了我们之前所描述的该疫苗对肿瘤化疗后具有微小残留病的小鼠的肿瘤抑制作用。