未经任何预先刺激的前列腺癌患者的T细胞对PSA衍生肽抗原的识别。
Recognition of PSA-derived peptide antigens by T cells from prostate cancer patients without any prior stimulation.
作者信息
Chakraborty Nitya G, Stevens Robert L, Mehrotra Shikhar, Laska Elizabeth, Taxel Pamela, Sporn Jonathan R, Schauer Peter, Albertsen Peter C
机构信息
Department of Medicine, University of Connecticut Health Center, 263 Farmington Avenue, Farmington, CT 06030-1315, USA.
出版信息
Cancer Immunol Immunother. 2003 Aug;52(8):497-505. doi: 10.1007/s00262-003-0377-8. Epub 2003 Jun 3.
Prostate-specific antigen (PSA) is a valuable marker antigen for prostate cancer. Lately considerable interest has been generated in the prospect of developing a vaccine for prostate cancer with PSA-derived peptide epitopes to induce cytotoxic T-cell (CTL) response. We report here that T cells capable of exhibiting PSA epitope-specific effector function-in their native state, i.e, without having to be further stimulated, in vitro-are detectable in more than half of the prostate cancer patients we studied. Ex vivo cultured autologous dendritic cells (DC) were used to present four HLA-A2-binding PSA peptide epitopes to freshly isolated peripheral blood lymphocytes (PBL) from patients and healthy volunteers. Ten out of 14 patients' PBL recognized at least one of the four peptides and 6 out of 10 patients' PBL recognized more than one peptide antigen as measured by IFN-gamma secretion upon stimulation of the PBL with the peptide antigen. Intracytoplasmic cytokine analysis for IFN-gamma in purified CD8(+) cells after stimulation with peptide antigens was tested in 6 patients and this technique demonstrated a similar response. Freshly isolated and purified CD8(+) cells when tested, also recognized the epitopes, as measured by IFN assay, when presented by transporter associated with antigen-processing (TAP) deficient T2 cells in an MHC-I restricted fashion. PBL from 9 normal donors when tested in identical fashion did not show any IFN-gamma production in recognition to the peptide antigens. Interestingly, neither of these CD8(+) T cells having IFN-gamma-producing ability did show any cytolytic activity in their native state against peptide loaded target cells or tumor cells when tested in cytotoxicity assay. In long term cocultures stimulation of purified CD8(+) T cells with matured DC pulsed with PSA peptides generated a PSA-specific CTL response in 4 of 6 patients studied and in 2 of 9 normal donors. While our observations of CTL generation are consistent with the prior reports that have demonstrated that specific CD8(+) CTL could be generated which recognize PSA-derived epitopes by in vitro stimulation by one means or another, this observation that IFN-gamma-producing CD8(+) T cells are present in patients which are antigen experienced, and do not require in vitro stimulation, is novel and has major implications for prostate cancer vaccine preparation.
前列腺特异性抗原(PSA)是前列腺癌的一种重要标志物抗原。最近,人们对开发一种以PSA衍生肽表位为基础的前列腺癌疫苗以诱导细胞毒性T细胞(CTL)反应产生了浓厚兴趣。我们在此报告,在我们研究的超过半数前列腺癌患者中,能够在其天然状态下(即无需进一步体外刺激)展现PSA表位特异性效应功能的T细胞是可检测到的。利用体外培养的自体树突状细胞(DC)将四种与HLA - A2结合的PSA肽表位呈递给从患者和健康志愿者新鲜分离的外周血淋巴细胞(PBL)。14例患者的PBL中有10例识别出四种肽中的至少一种,10例患者的PBL中有6例在肽抗原刺激PBL后通过IFN -γ分泌检测发现识别出一种以上的肽抗原。对6例患者在用肽抗原刺激后纯化的CD8(+)细胞中IFN -γ进行胞内细胞因子分析,该技术显示出类似的反应。新鲜分离和纯化的CD8(+)细胞在检测时,当由与抗原加工相关的转运体(TAP)缺陷的T2细胞以MHC - I限制性方式呈递表位时,通过IFN检测也能识别这些表位。以相同方式检测的9名正常供体的PBL在识别肽抗原时未显示出任何IFN -γ产生。有趣的是,这些具有产生IFN -γ能力的CD8(+) T细胞在细胞毒性试验中检测时,在其天然状态下对负载肽的靶细胞或肿瘤细胞均未显示出任何细胞溶解活性。在长期共培养中,用PSA肽脉冲成熟的DC刺激纯化的CD8(+) T细胞,在研究的6例患者中有4例以及9名正常供体中有2例产生了PSA特异性CTL反应。虽然我们对CTL产生的观察结果与先前的报告一致(先前报告表明通过某种方式体外刺激可产生识别PSA衍生表位的特异性CD8(+) CTL),但这一观察结果,即在经历过抗原的患者中存在产生IFN -γ的CD8(+) T细胞且无需体外刺激,是新颖的,并且对前列腺癌疫苗制备具有重要意义。