Suppr超能文献

非小细胞肺癌中癌胚抗原表达及特异性细胞毒性T淋巴细胞反应

Cancer/testis antigen expression and specific cytotoxic T lymphocyte responses in non small cell lung cancer.

作者信息

Groeper Célia, Gambazzi Franco, Zajac Paul, Bubendorf Lukas, Adamina Michel, Rosenthal Rachel, Zerkowski Hans-Reinhard, Heberer Michael, Spagnoli Giulio C

机构信息

Institute for Surgical Research and Hospital Management, Department of Research, University Hospital, Basel, Switzerland.

出版信息

Int J Cancer. 2007 Jan 15;120(2):337-43. doi: 10.1002/ijc.22309.

Abstract

Non small cell lung cancers (NSCLC) express cancer/testis antigens (CTA) genes and MAGE-A expression correlates with poor prognosis in squamous cell carcinomas. We addressed cytotoxic T lymphocytes (CTL) responses to HLA class I restricted CTA epitopes in TIL from NSCLC in an unselected group of 33 patients consecutively undergoing surgery. Expression of MAGE-A1, -A2, -A3, -A4, -A10, -A12 and NY-ESO-1 CTA genes was tested by quantitative RT-PCR. Monoclonal antibodies (MAb) recognizing MAGE-A and NY-ESO-1 CTA were used to detect CTA by immunohistochemistry. CD8(+) TIL obtained from tumors upon culture with anti CD3 and anti CD28 mAb and IL-2 were stimulated with autologous mature DC (mDC) and HLA-A0101 restricted MAGE-A1(161-169) or MAGE-A3(168-176) peptides or HLA-A0201 restricted MAGE-A4(230-239), MAGE-A10(254-262), NY-ESO-1(157-165) or multi-MAGE-A (YLEYRQVPV) peptides or a recombinant vaccinia virus (rVV) encoding MAGE-A and NY-ESO-1 HLA-A0201 restricted epitopes and CD80 co-stimulatory molecule. Specificity was assessed by (51)Cr release and multimer staining. At least one CTA gene was expressed in tumors from 15/33 patients. In 10 specimens, at least 4 CTA genes were concomitantly expressed. These data were largely confirmed by immunohistochemistry. TIL were expanded from 26/33 specimens and CTA-specific CTL activity was detectable in 7/26 TIL. In 6, however, specific cytotoxicity was weak, (<40% lysis at a 50:1 E:T ratio) and multimer staining was undetectable. In one case, high (>60% lysis at 50:1 E:T ratio) MAGE-A10(254-262) specific, HLA-A0201 restricted response was observed. Supportive evidence was provided by corresponding multimer staining. Although CTA genes are frequently expressed in NSCLC, detection of CTL reactivity against CTA epitopes in TIL from nonimmunized NSCLC patients represents a rare event.

摘要

非小细胞肺癌(NSCLC)表达癌胚抗原(CTA)基因,MAGE - A的表达与鳞状细胞癌的不良预后相关。我们在一组连续接受手术的33例未经选择的患者中,研究了细胞毒性T淋巴细胞(CTL)对NSCLC肿瘤浸润淋巴细胞(TIL)中HLA - I类限制性CTA表位的反应。通过定量逆转录聚合酶链反应检测MAGE - A1、- A2、- A3、- A4、- A10、- A12和NY - ESO - 1 CTA基因的表达。使用识别MAGE - A和NY - ESO - 1 CTA的单克隆抗体(MAb)通过免疫组织化学检测CTA。用抗CD3和抗CD28单克隆抗体及白细胞介素-2培养从肿瘤中获得的CD8(+) TIL,并用自体成熟树突状细胞(mDC)和HLA - A0101限制性MAGE - A1(161 - 169)或MAGE - A3(168 - 176)肽或HLA - A0201限制性MAGE - A4(230 - 239)、MAGE - A10(254 - 262)、NY - ESO - 1(157 - 165)或多MAGE - A(YLEYRQVPV)肽或编码MAGE - A和NY - ESO - 1 HLA - A0201限制性表位及CD80共刺激分子的重组痘苗病毒(rVV)进行刺激。通过铬(51)释放和多聚体染色评估特异性。15/33例患者的肿瘤中至少表达一种CTA基因。在10个标本中,至少4种CTA基因同时表达。这些数据在很大程度上得到了免疫组织化学的证实。从26/33个标本中扩增出TIL,在7/26的TIL中可检测到CTA特异性CTL活性。然而,在6例中,特异性细胞毒性较弱(在50:1的效应细胞与靶细胞比例下裂解率<40%)且多聚体染色未检测到。在1例中,观察到高(在50:1的效应细胞与靶细胞比例下裂解率>60%)的MAGE - A10(254 - 262)特异性、HLA - A0201限制性反应。相应的多聚体染色提供了支持性证据。尽管CTA基因在NSCLC中经常表达,但在未免疫的NSCLC患者的TIL中检测到针对CTA表位的CTL反应是罕见的事件。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验