Phase 1 clinical study of cyclophilin B peptide vaccine for patients with lung cancer

被引:32
作者
Gohara, R
Imai, N
Rikimaru, T
Yamada, A
Hida, N
Ichiki, M
Kawamoto, M
Matsunaga, K
Ashihara, J
Yano, S
Tamura, M
Ohkouchi, S
Yamana, H
Oizumi, K
Itoh, K
机构
[1] Kurume Univ, Sch Med, Dept Immunol, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ, Sch Med, Dept Internal Med, Kurume, Fukuoka 830, Japan
[3] Kurume Univ, Sch Med, Dept Surg, Kurume, Fukuoka 830, Japan
[4] Res Ctr Innovat Canc Therapy, Canc Vaccine Dev Div, Fukuoka, Japan
关键词
cytotoxic T lymphocytes-peptides; immunotherapy; lung cancer; phase; 1; study;
D O I
10.1097/00002371-200209000-00008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclophilin B (CypB) possesses two antigenic epitopes (CypB(84-92) and CypB(91-99)) recognized by HLA-A24-restricted and tumor-specific cytotoxic T lymphocytes (CTLs). To determine the safety of CypB-derived peptides and its ability to generate antitumor immune responses, patients with advanced lung cancer received subcutaneous vaccinations of these peptides or their modified peptides. All 16 patients Were vaccinated With CypB(91-99) or its modified peptide, whereas only two patients were vaccinated With the modified CypB(84-92), as immediate-type hypersensitivity to CypB(84-92), or its modified peptide was observed in the remaining patients. No severe adverse events were associated with the vaccination. No significant increase in cellular responses to either peptides or tumor cells was observed in the postvaccination PBMCS by the conventional CTL assays in any patients tested. These results suggest that the vaccination of CypB(91-99) peptide was safe, but failed to induce objective immune responses at this regimen.
引用
收藏
页码:439 / 444
页数:6
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