Mine Takashi, Gouhara Rumi, Hida Naoya, Imai Nobue, Azuma Kouichi, Rikimaru Touru, Katagiri Kazuko, Nishikori Misa, Sukehiro Aki, Nakagawa Masami, Yamada Akira, Aizawa Hisamichi, Shirouzu Kazuo, Itoh Kyogo, Yamana Hideaki
Department of Immunology, Department of Surgery, Kurume University School of Medicine, Kurume 830-0011, Japan.
Cancer Sci. 2003 Jun;94(6):548-56. doi: 10.1111/j.1349-7006.2003.tb01481.x.
Recent clinical trials of peptide vaccine for cancer patients have rarely resulted in tumor regression. One of the reasons for this failure could be an insufficient induction of anti-tumor responses in these regimens, in which peptide-specific memory cytotoxic T lymphocytes (CTLs) were not measured prior to vaccination. We investigated in this study whether pre-vaccination measurement of peptide-specific CTLs can provide any advantages in lung cancer patients receiving peptide vaccination with regard to safety and immunological responses. Ten patients with advanced lung cancer received vaccination with peptides under a regimen of CTL precursor-oriented vaccination, in which pre-vaccination peripheral blood mononuclear cells (PBMCs) were at first screened for reactivity in vitro to each of 14 peptides, followed by in vivo administration of only the reactive peptides. Profiles of the vaccinated peptides varied markedly among the 10 patients. This regimen was generally well-tolerated, although local skin reactions, diarrhea, and colitis were observed in 8, 2, and 1 patient, respectively. Increased CTL responses against the immunized peptides and tumor cells were observed in the post-vaccination PBMCs from 4 of 8 and 3 of 10 patients tested, respectively. Peptide-specific IgG became detectable in post-vaccination sera in 4 of 10 patients tested, and these 4 patients had a long progression-free survival. Furthermore, the median survival time of 9 patients with non-small cell lung cancer was 668.0 +/- 164.2 days. These results encourage further development of CTL precursor-oriented peptide vaccination for lung cancer patients.
近期针对癌症患者的肽疫苗临床试验很少能使肿瘤消退。这种失败的原因之一可能是这些方案中抗肿瘤反应的诱导不足,在这些方案中,接种疫苗前未检测肽特异性记忆细胞毒性T淋巴细胞(CTL)。在本研究中,我们调查了对于接受肽疫苗接种的肺癌患者,接种前检测肽特异性CTL在安全性和免疫反应方面是否具有任何优势。10例晚期肺癌患者接受了以CTL前体为导向的疫苗接种方案的肽疫苗接种,其中接种前首先在体外筛选外周血单个核细胞(PBMC)对14种肽中每种肽的反应性,然后仅体内给予有反应的肽。10例患者中接种的肽谱差异显著。该方案总体耐受性良好,尽管分别有8例、2例和1例患者出现局部皮肤反应、腹泻和结肠炎。在分别检测的8例患者中的4例和10例患者中的3例接种后PBMC中观察到针对免疫肽和肿瘤细胞的CTL反应增加。在检测的10例患者中的4例接种后血清中可检测到肽特异性IgG,这4例患者有较长的无进展生存期。此外,9例非小细胞肺癌患者的中位生存时间为668.0±164.2天。这些结果鼓励进一步开发针对肺癌患者的以CTL前体为导向的肽疫苗接种。