Back to Search Start Over

Heteroclitic serological response in esophageal and prostate cancer patients after NY-ESO-1 protein vaccination

Authors :
Nami Okazaki
Lloyd J. Old
Hiroshi Miyata
Sacha Gnjatic
Hiroyoshi Nishikawa
Yurika Nakamura
Makoto Yamasaki
Naoaki Mizuno
Shinichi Fujiwara
Gerd Ritter
Eiichi Nakayama
Junji Kawada
Erika Ritter
Midori Isobe
Achim A. Jungbluth
Hisashi Wada
Roger Murphy
Yuichiro Doki
Linda Pan
Akiko Uenaka
Takashi Saika
Ralph Venhaus
Source :
International Journal of Cancer. 130:584-592
Publication Year :
2011
Publisher :
Wiley, 2011.

Abstract

NY-ESO-1 is a prototypic cancer/testis antigen. In a recent phase I clinical trial, we vaccinated 13 patients bearing NY-ESO-1-expressing tumors with a complex of cholesterol-bearing hydrophobized pullulan (CHP) and NY-ESO-1 protein (CHP-NY-ESO-1) and showed efficient induction of NY-ESO-1 antibody, and CD4 and CD8 T cell responses using peripheral blood from the patients. In our study, we analyzed heteroclitic serological responses in those patients after vaccination. Serological response against 11 tumor antigens including MAGE-A1, MAGE-A3, MAGE-A4, CT7/MAGEC1, CT10/MAGEC2, CT45, CT46/HORMAD1, SOX2, SSX2, XAGE1B and p53 was examined by enzyme-linked immunosorbent assay (ELISA) using sera from ten vaccinated patients. Expression of tumor antigens was determined by reverse transcription-polymerase chain reaction or immunohistochemistry. Eight of nine patients who showed antibody responses against NY-ESO-1 also showed an antibody response against at least 1 of these 11 tumor antigens after vaccination. In one patient, seven tumor antigens were recognized. Specificity analysis of the antibody response by ELISA using control recombinant proteins and synthetic peptides and by Western blot showed that the response was not against His6-tag and/or bacterial products included in a preparation of CHP-NY-ESO-1 used for vaccination. Thus, heteroclitic serological responses appear to be indicative of the overall immune response against the tumor, and their analysis could be useful for immune monitoring in cancer vaccine.

Details

ISSN :
00207136
Volume :
130
Database :
OpenAIRE
Journal :
International Journal of Cancer
Accession number :
edsair.doi.dedup.....cb1aea8bd6589167ab349733f75ef295
Full Text :
https://doi.org/10.1002/ijc.26074