Kim D, Monie A, Tsai Y-C, He L, Wang M-C, Hung C-F, Wu T-C
Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, MD, USA.
Gene Ther. 2008 Aug;15(16):1176-83. doi: 10.1038/gt.2008.79. Epub 2008 May 8.
Multimodality treatments that combine conventional cancer therapies with antigen-specific immunotherapy have emerged as promising approaches for the control of cancer. In the current study, we have explored the effect of doxorubicin on the antigen-specific immune responses generated in mice vaccinated with calreticulin (CRT)/E6 and/or Ii-PADRE DNA. We observed that pretreatment with doxorubicin suppressed the E6-specific CD8+ T-cell immune responses generated by CRT/E6 DNA vaccination in vaccinated mice. In contrast, pretreatment with doxorubicin enhanced the PADRE-specific CD4+ T-cell immune responses generated by Ii-PADRE DNA vaccination. Furthermore, coadministration of Ii-PADRE DNA could not only reverse the suppression, but also enhanced the E6-specific CD8+ T-cell responses in CRT/E6-vaccinated mice pretreated with doxorubicin. Finally, treatment with doxorubicin followed by CRT/E6 combined with Ii-PADRE DNA vaccination led to enhanced antitumor effects and prolonged survival in TC-1 tumor-bearing mice. The clinical implications of the current study are discussed.
将传统癌症疗法与抗原特异性免疫疗法相结合的多模态治疗已成为控制癌症的有前景的方法。在当前研究中,我们探究了阿霉素对用钙网蛋白(CRT)/E6和/或Ii-PADRE DNA疫苗接种的小鼠中产生的抗原特异性免疫反应的影响。我们观察到,阿霉素预处理抑制了接种疫苗的小鼠中CRT/E6 DNA疫苗接种产生的E6特异性CD8 + T细胞免疫反应。相反,阿霉素预处理增强了Ii-PADRE DNA疫苗接种产生的PADRE特异性CD4 + T细胞免疫反应。此外,Ii-PADRE DNA的共同给药不仅可以逆转这种抑制作用,还可以增强用阿霉素预处理的CRT/E6疫苗接种小鼠中的E6特异性CD8 + T细胞反应。最后,用阿霉素治疗后再进行CRT/E6与Ii-PADRE DNA疫苗接种导致TC-1荷瘤小鼠的抗肿瘤作用增强和生存期延长。本文讨论了当前研究的临床意义。