IFN-gamma gene transfer restores HLA-class I expression and MAGE-3 antigen presentation to CTL in HLA-deficient small cell lung cancer

被引:46
作者
Traversari, C
Meazza, R
Coppolecchia, M
Basso, S
Verrecchia, A
vanderBruggen, P
Ardizzoni, A
Gaggero, A
Ferrini, S
机构
[1] IST NAZL RIC CANC,CBA,I-16132 GENOA,ITALY
[2] DIBIT HS RAFFAELE,MILAN,ITALY
[3] UNIV GENOA,DIPARTIMENTO ONCOL SPERIMENTALE & CLIN,GENOA,ITALY
[4] LUDWIG INST CANC RES,BRUSSELS BRANCH,BRUSSELS,BELGIUM
关键词
interferon-gamma; antigen presentation; tumor-associated antigens; cytolytic T lymphocytes; small cell lung cancer;
D O I
10.1038/sj.gt.3300489
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we have analyzed the possibility of inducing I cell responses against small cell lung cancer (SCLC), a still incurable tumor, by cytokine gene transfer approaches. By RT-PCR analysis most SCLC expressed the CTL-defined tumor antigens MAGE-3 (10/11), MAGE-1 (7/11) and less frequently BAGE (4/11) and GAGE1,2 (4/11). Although the surface expression of HLA class I molecules was low on most SCLC, thus preventing CTL recognition, treatment of the cells with IFN-gamma enhanced HLA-class I levels in all cases. Two MAGE3(+) SCLC cell lines displaying the A2 HLA-class I allele, involved in MAGE-3 antigen presentation to CTL, were stably transfected with the IFN-gamma gene (alone or co-transfected with IL-2). IFN-gamma-transfected cells displayed a clearcut increase in expression of HLA-class I and beta(2) microglobulin at both protein and mRNA level and of TAP-1 and TAP-2 mRNA. Perhaps more importantly, IFN-gamma transfected cells were recognized by the MAGE-3-specific, A2-restricted antimelanoma CTL clone 297/22, while unmodified cells or cells transfected with the IL-2 gene alone were not. These data indicate that IFN-gamma gene transfection into HLA-deficient SCLC cells is able to restore their ability to present endogenous tumor antigens to CTL and that IFN-gamma gene transfer approaches may be attempted to induce specific CTL responses in SCLC.
引用
收藏
页码:1029 / 1035
页数:7
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