| Literature DB >> 24509171 |
Hisashi Wada1, Midori Isobe, Kazuhiro Kakimi, Yu Mizote, Shingo Eikawa, Eiichi Sato, Nagio Takigawa, Katsuyuki Kiura, Kazuhide Tsuji, Keiji Iwatsuki, Makoto Yamasaki, Hiroshi Miyata, Hirokazu Matsushita, Heiichiro Udono, Yasuyuki Seto, Kazuhiro Yamada, Hiroyoshi Nishikawa, Linda Pan, Ralph Venhaus, Mikio Oka, Yuichiro Doki, Eiichi Nakayama.
Abstract
We conducted a clinical trial of an NY-ESO-1 cancer vaccine using 4 synthetic overlapping long peptides (OLP; peptides #1, 79-108; #2, 100-129; #3, 121-150; and #4, 142-173) that include a highly immunogenic region of the NY-ESO-1 molecule. Nine patients were immunized with 0.25 mg each of three 30-mer and a 32-mer long NY-ESO-1 OLP mixed with 0.2 KE Picibanil OK-432 and 1.25 mL Montanide ISA-51. The primary endpoints of this study were safety and NY-ESO-1 immune responses. Five to 18 injections of the NY-ESO-1 OLP vaccine were well tolerated. Vaccine-related adverse events observed were fever and injection site reaction (grade 1 and 2). Two patients showed stable disease after vaccination. An NY-ESO-1-specific humoral immune response was observed in all patients and an antibody against peptide #3 (121-150) was detected firstly and strongly after vaccination. NY-ESO-1 CD4 and CD8 T-cell responses were elicited in these patients and their epitopes were identified. Using a multifunctional cytokine assay, the number of single or double cytokine-producing cells was increased in NY-ESO-1-specific CD4 and CD8 T cells after vaccination. Multiple cytokine-producing cells were observed in PD-1 (-) and PD-1 (+) CD4 T cells. In conclusion, our study indicated that the NY-ESO-1 OLP vaccine mixed with Picibanil OK-432 and Montanide ISA-51 was well tolerated and elicited NY-ESO-1-specific humoral and CD4 and CD8 T-cell responses in immunized patients.Entities:
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Year: 2014 PMID: 24509171 DOI: 10.1097/CJI.0000000000000017
Source DB: PubMed Journal: J Immunother ISSN: 1524-9557 Impact factor: 4.456