Viral Infectious Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejon, Korea.
Cancer Immunol Immunother. 2010 Nov;59(11):1727-37. doi: 10.1007/s00262-010-0903-4. Epub 2010 Aug 13.
Given that local cell-mediated immunity (CMI) against the human papillomavirus type 16 E6 (HPV16 E6) protein is important for eradication of HPV16 E6-expressing cancer cells in the cervical mucosa, the HPV16 E6 protein may be a target for the mucosal immunotherapy of cervical cancer. Here, we expressed the HPV16 E6 antigen on Lactobacillus casei (L. casei) and investigated E6-specific CMI following oral administration of the L. casei-PgsA-E6 to mice. Surface expression of HPV16 E6 antigens was confirmed and mice were orally inoculated with the L. casei-PgsA or the L. casei-PgsA-E6. Compared to the L. casei-PgsA-treated mice, significantly higher levels of serum IgG and mucosal IgA were observed in L. casei-PgsA-E6-immunized mice; these differences were significantly enhanced after boost. Consistent with this, systemic and local CMI were significantly increased after the boost, as shown by increased counts of IFN-gamma-secreting cells in splenocytes, mesenteric lymph nodes (MLN), and vaginal samples. Furthermore, in the TC-1 tumor model, animals receiving the orally administered L. casei-PgsA-E6 showed reduced tumor size and increased survival rate versus mice receiving control (L. casei-PgsA) immunization. We also found that L. casei-PgsA-E6-induced antitumor effect was decreased by in vivo depletion of CD4(+) or CD8(+) T cells. Collectively, these results indicate that the oral administration of lactobacilli bearing the surface-displayed E6 protein induces T cell-mediated cellular immunity and antitumor effects in mice.
鉴于针对人乳头瘤病毒 16 型 E6(HPV16 E6)蛋白的局部细胞介导免疫(CMI)对于消除宫颈黏膜中 HPV16 E6 表达的癌细胞很重要,HPV16 E6 蛋白可能成为宫颈癌黏膜免疫治疗的靶点。在这里,我们在干酪乳杆菌(L. casei)上表达了 HPV16 E6 抗原,并研究了口服 L. casei-PgsA-E6 后 E6 特异性 CMI。确认 HPV16 E6 抗原的表面表达,并将小鼠口服接种 L. casei-PgsA 或 L. casei-PgsA-E6。与 L. casei-PgsA 处理的小鼠相比,L. casei-PgsA-E6 免疫的小鼠中观察到血清 IgG 和黏膜 IgA 水平明显升高;在加强后,这些差异显著增强。与此一致,全身和局部 CMI 在加强后显著增加,表现为脾细胞、肠系膜淋巴结(MLN)和阴道样本中 IFN-γ分泌细胞计数增加。此外,在 TC-1 肿瘤模型中,与接受对照(L. casei-PgsA)免疫的小鼠相比,接受口服给予的 L. casei-PgsA-E6 的动物显示肿瘤体积减小和生存率提高。我们还发现,体内耗尽 CD4(+)或 CD8(+)T 细胞会降低 L. casei-PgsA-E6 诱导的抗肿瘤作用。总之,这些结果表明,携带表面展示 E6 蛋白的乳杆菌的口服给药可在小鼠中诱导 T 细胞介导的细胞免疫和抗肿瘤作用。