Toubaji Antoun, Hill Sarah, Terabe Masaki, Qian Jiahua, Floyd Tamara, Simpson R Mark, Berzofsky Jay A, Khleif Samir N
Cancer Vaccine Section, Vaccine Branch, NCI, NIH, Bethesda, MD, United States.
Vaccine. 2007 Aug 1;25(31):5882-91. doi: 10.1016/j.vaccine.2007.05.040. Epub 2007 Jun 12.
Many strategies have been used to enhance the peptide vaccine immune response and to establish therapeutic benefits. This includes the utilization of cytokines to improve antigen presentation or enhance T cell response. Here, we have tested the combination of GM-CSF and IL-2 as locally administered adjuvant to enhance the immune response to the HPV16 E7 peptide. Female C57BL/6 mice were immunized intradermally with a 9-mer HPV16 E7 peptide (aa: 49-57) alone, or in combination with GM-CSF, IL-2, or both cytokines. Specific immune responses were measured by ELISA and Chromium-Release Assays. Furthermore, therapeutic effects of these vaccines and long term tumor protection were assessed in mice bearing established tumors. We showed that GM-CSF and IL-2, when co-administered locally in an emulsion with peptide, exert a synergistic effect in enhancing the immune response to the antigen. This combination induced higher CTL and cytokine release responses and did not increase the T(reg) population. Therapeutic intervention with this synergistic combination led to a complete response of established tumors. Furthermore, this combination induced a memory response which protected mice against subsequent additional tumor challenge. We identified a new vaccine adjuvant, a local combination of GM-CSF and IL-2, which is synergistic in enhancing peptide specific immune response through local effect without increasing T(reg) cells. This immune response was found to be long lasting and protective in tumor bearing mice.
人们已经采用了多种策略来增强肽疫苗的免疫反应并确立其治疗效果。这包括利用细胞因子来改善抗原呈递或增强T细胞反应。在此,我们测试了将GM-CSF和IL-2作为局部给药佐剂,以增强对HPV16 E7肽的免疫反应。雌性C57BL/6小鼠分别单独皮内注射9聚体HPV16 E7肽(氨基酸:49-57),或与GM-CSF、IL-2或两种细胞因子联合注射。通过酶联免疫吸附测定(ELISA)和铬释放试验来检测特异性免疫反应。此外,在已形成肿瘤的小鼠中评估了这些疫苗的治疗效果和长期肿瘤保护作用。我们发现,GM-CSF和IL-2与肽在乳剂中局部联合给药时,在增强对抗原的免疫反应方面发挥协同作用。这种联合诱导了更高的细胞毒性T淋巴细胞(CTL)和细胞因子释放反应,并且没有增加调节性T细胞(T(reg))群体。用这种协同组合进行治疗干预导致已形成的肿瘤完全消退。此外,这种组合诱导了记忆反应,可保护小鼠免受随后的额外肿瘤攻击。我们鉴定出一种新的疫苗佐剂,即GM-CSF和IL-2的局部组合,其通过局部作用在增强肽特异性免疫反应方面具有协同作用,且不会增加T(reg)细胞。在荷瘤小鼠中发现这种免疫反应具有持久性和保护性。