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一项针对结直肠癌患者的以细胞毒性T淋巴细胞前体为导向的肽疫苗的I期试验。

A phase I trial of cytotoxic T-lymphocyte precursor-oriented peptide vaccines for colorectal carcinoma patients.

作者信息

Sato Y, Maeda Y, Shomura H, Sasatomi T, Takahashi M, Une Y, Kondo M, Shinohara T, Hida N, Katagiri K, Sato K, Sato M, Yamada A, Yamana H, Harada M, Itoh K, Todo S

机构信息

First Department of Surgery, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Br J Cancer. 2004 Apr 5;90(7):1334-42. doi: 10.1038/sj.bjc.6601711.

DOI:10.1038/sj.bjc.6601711
PMID:15054451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2409683/
Abstract

In most protocols of peptide-based vaccination, no consideration has been paid to whether or not peptide-specific cytotoxic T-lymphocyte (CTL) precursors are pre-existent in cancer patients. Initiation of immune boosting through vaccination is better than that of immune priming to induce prompt and strong immunity. In this study, 10 human histocompatibility leukocyte antigen-A24(+) patients with advanced colorectal carcinomas were treated with up to four peptides that had been positive for pre-vaccination measurement of peptide-specific CTL precursors in the circulation (CTL precursor-oriented peptide vaccine). No severe adverse effect was observed, although local pain and fever of grade I or II were observed. Post-vaccination peripheral blood mononuclear cells (PBMCs) from five patients demonstrated an increased peptide-specific immune response to the peptides. Increased CTL response to cancer cells was detected in post-vaccination PBMCs of five patients. Antipeptide immunoglobulin G became detectable in post-vaccination sera of seven patients. Three patients developed a positive delayed-type hypersensitivity response to at least one of the peptides administrated. One patient was found to have a partial response; another had a stable disease, sustained through 6 months. These results encourage further development of CTL precursor-oriented vaccine for colorectal cancer patients.

摘要

在大多数基于肽的疫苗接种方案中,并未考虑癌症患者体内是否预先存在肽特异性细胞毒性T淋巴细胞(CTL)前体。通过疫苗接种启动免疫增强比免疫初次启动更能诱导迅速而强烈的免疫反应。在本研究中,10名人类组织相容性白细胞抗原A24(+)的晚期结直肠癌患者接受了多达四种肽的治疗,这些肽在循环中肽特异性CTL前体的疫苗接种前测量中呈阳性(以CTL前体为导向的肽疫苗)。尽管观察到I级或II级局部疼痛和发热,但未观察到严重不良反应。五名患者接种疫苗后的外周血单核细胞(PBMC)对这些肽的肽特异性免疫反应增强。在五名患者接种疫苗后的PBMC中检测到对癌细胞的CTL反应增强。在七名患者接种疫苗后的血清中可检测到抗肽免疫球蛋白G。三名患者对至少一种给药肽产生了阳性迟发型超敏反应。一名患者出现部分缓解;另一名患者病情稳定,持续了6个月。这些结果鼓励进一步开发针对结直肠癌患者的以CTL前体为导向的疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/93be4edf2957/90-6601711f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/03e887286ecb/90-6601711f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/5e9b3f7dff2a/90-6601711f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/02269ac20c13/90-6601711f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/93be4edf2957/90-6601711f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/03e887286ecb/90-6601711f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/5e9b3f7dff2a/90-6601711f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/02269ac20c13/90-6601711f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/924e/2409683/93be4edf2957/90-6601711f4.jpg

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Immunological evaluation of peptide vaccination for patients with gastric cancer based on pre-existing cellular response to peptide.
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