Translational Surgical Pathology, Laboratory of Pathology, CCR, NCI, NIH, Bethesda, MD 20892.
Urologic Oncology Branch, CCR, NCI, NIH, Bethesda, MD 20892.
Hum Pathol. 2018 Aug;78:72-78. doi: 10.1016/j.humpath.2018.04.013. Epub 2018 Apr 30.
Immunotherapy is a novel treatment for many tumors including prostate cancer. Little is known about the histological changes in prostate biopsies caused by the prostate-specific antigen (PSA)-based vaccine. This study evaluated the histopathological effects in prostate biopsies of recombinant fowlpox (rF) virus-based vaccine engineered to present the PSA and 3 costimulatory molecules (collectively labeled as PSA-TRICOM). This vaccine has shown that it can break tolerance of the PSA, and its administration directly into a tumor enables the affected tumor cells to act as antigen-presenting cells activating new T cells and broadening the immune response to recognize and kill tumor. We studied 10 patients with recurrent prostate cancer who had failed radiation therapy and/or androgen-deprivation therapy. Pre- and posttreatment biopsies were compared. Posttreatment biopsies induced 8 cases with residual adenocarcinoma despite evidences of treatment effect and inflammation, 2 cases did not show any residual tumor, and 1 one case did not have any inflammatory infiltrate or any evidence of treatment effect. The inflammatory infiltrate varied from mild to severe and was composed of mononuclear cells. Greater numbers of infiltrating CD8+ lymphocytes were identified around prostatic glands and within the epithelial lining. The most remarkable feature was the presence of increased eosinophils around the glands and stroma. Three cases showed areas of necrosis surrounded by lymphocytes and palisading epithelioid macrophages arranged in granuloma-like pattern with multinucleated giant cells. This description of these morphological changes induced by the PSA-TRICOM will help to interpret the results of future intratumoral vaccine therapy trials.
免疫疗法是一种治疗多种肿瘤的新方法,包括前列腺癌。目前对于基于前列腺特异抗原 (PSA) 的疫苗引起的前列腺活检组织学变化知之甚少。本研究评估了基于重组禽痘病毒 (rF) 的疫苗在前列腺活检中的组织病理学效应,该疫苗工程化表达 PSA 和 3 个共刺激分子(统称为 PSA-TRICOM)。该疫苗已显示能够打破 PSA 的耐受,并且其直接施用于肿瘤可使受影响的肿瘤细胞充当抗原呈递细胞,激活新的 T 细胞并扩大免疫反应以识别和杀死肿瘤。我们研究了 10 例复发性前列腺癌患者,这些患者在接受放射治疗和/或雄激素剥夺治疗后复发。比较了治疗前后的活检。尽管有治疗效果和炎症的证据,但治疗后活检仍诱导 8 例残留腺癌,2 例未显示任何残留肿瘤,1 例无任何炎症浸润或治疗效果的证据。炎症浸润从轻度到重度不等,由单核细胞组成。在前列腺腺体周围和上皮衬里内鉴定出更多的浸润性 CD8+淋巴细胞。最显著的特征是腺体和基质周围嗜酸性粒细胞增多。3 例表现为淋巴细胞包围的坏死区和呈栅栏状上皮样巨噬细胞排列成类似于肉芽肿的模式,伴有多核巨细胞。这种对 PSA-TRICOM 诱导的这些形态变化的描述将有助于解释未来肿瘤内疫苗治疗试验的结果。