Woll Michael M, Hueman Matthew T, Ryan Gayle B, Ioannides Constantin G, Henderson Charles G, Sesterhan Isabelle A, Shrivasta Shiv, McLeod David G, Moul Judd W, Peoples George E
Divisions of General Surgery and Urology, Department of Surgery, Walter Reed Army Medical Center, Washington, DC 20307, USA.
Int J Oncol. 2004 Dec;25(6):1769-80.
The HER2/neu protein is over-expressed in multiple epithelial tumors and the source of immunogenic peptides currently under investigation in vaccine trials in ovarian and breast cancers. We sought to define the correlation between HER2/neu expression and risk for prostate cancer recurrence and then determine the potential efficacy of anti-HER2/neu vaccination in prostate cancer patients at risk for recurrence. The risk for prostate-specific antigen (PSA) recurrence in 95 patients undergoing prostatectomy at the Walter Reed Army Medical Center (WRAMC) was calculated and correlated to HER2/neu expression, as determined by immunohistochemical staining. Peripheral blood lymphocytes (PBL) were then isolated from six consecutive human leukocyte antigen (HLA) A2+ patients with HER2/neu+ prostate tumors. These PBL were grown in parallel cultures and stimulated either with no peptide, HER2/neu E75 peptide, or control peptide. The cultures were compared for stimulated proliferation, induced peptide-specific cytotoxicity and tumor-specific cytotoxicity. When assessed by risk group, 69% of the high risk patients' tumors over-expressed HER2/neu compared to 47% of the intermediate risk group (p<0.05). Evaluation of the in vitro immune response of PBL isolated from six consecutive prostate cancer patients revealed a statistically significant increase in E75-stimulated lymphocytic proliferation. E75-stimulated lymphocytes demonstrated an E75-specific cytolytic response in 6/6 prostate cancer patients that increased with successive stimulations. Moreover, these E75-specific lymphocytes also demonstrated tumor-specific lysis against HER2/neu-expressing prostate cancer cell lines. The majority of prostate cancer patients at high risk for recurrence have HER2/neu expressing tumors. Hence, HER2/neu is a viable target for immunotherapeutics such as preventative immunization strategies with HER2/neu peptide vaccines.
HER2/neu蛋白在多种上皮肿瘤中过度表达,是目前卵巢癌和乳腺癌疫苗试验中正在研究的免疫原性肽的来源。我们试图确定HER2/neu表达与前列腺癌复发风险之间的相关性,然后确定抗HER2/neu疫苗接种对有复发风险的前列腺癌患者的潜在疗效。计算了在沃尔特·里德陆军医疗中心(WRAMC)接受前列腺切除术的95例患者中前列腺特异性抗原(PSA)复发的风险,并将其与通过免疫组织化学染色确定的HER2/neu表达相关联。然后从六名连续的人类白细胞抗原(HLA)A2+且HER2/neu+前列腺肿瘤患者中分离外周血淋巴细胞(PBL)。这些PBL在平行培养物中生长,并用无肽、HER2/neu E75肽或对照肽进行刺激。比较培养物的刺激增殖、诱导的肽特异性细胞毒性和肿瘤特异性细胞毒性。按风险组评估时,69%的高风险患者肿瘤过度表达HER2/neu,而中度风险组为47%(p<0.05)。对从六名连续前列腺癌患者中分离的PBL的体外免疫反应评估显示,E75刺激的淋巴细胞增殖有统计学显著增加。E75刺激的淋巴细胞在6/6例前列腺癌患者中表现出E75特异性溶细胞反应,且随着连续刺激而增加。此外,这些E75特异性淋巴细胞还对表达HER2/neu的前列腺癌细胞系表现出肿瘤特异性裂解。大多数有高复发风险的前列腺癌患者的肿瘤表达HER2/neu。因此,HER2/neu是免疫治疗的一个可行靶点,例如用HER2/neu肽疫苗进行预防性免疫策略。