INSERM, U892, Research Center in Oncology Nantes-Angers, France.
Cell Adh Migr. 2010 Jan-Mar;4(1):153-61. doi: 10.4161/cam.4.1.11361. Epub 2010 Jan 30.
Malignant pleural mesothelioma (MPM) is a rare malignancy of the pleura with a very poor prognosis. Treatments evaluated for malignant mesothelioma, including chemotherapy, radiotherapy and surgery are of limited efficacy. However, the fact that the tumors of some patients with MPM regress spontaneously or respond to immunotherapy suggests that the immune system may respond to MPM under some circumstances. In this respect, animal studies have demonstrated immunoreactivity of MPM to different immunotherapies. In the case of MPM, several clinical studies have demonstrated a correlation between the presence of a lymphocyte infiltrate and a better prognosis and humoral response directed against specific antigens related to tumor. Thus, MPM immunotherapy is undoubtedly a highly promising but also very challenging approach to the treatment of this disease that has slipped through the defense lines of the immune system. This article reviews past and recent developments of the clinical strategies that concern immunotherapy of mesothelioma.
恶性胸膜间皮瘤(MPM)是一种罕见的胸膜恶性肿瘤,预后极差。已经评估了多种治疗方法,包括化疗、放疗和手术,但疗效有限。然而,一些 MPM 患者的肿瘤自发消退或对免疫疗法有反应的事实表明,在某些情况下免疫系统可能会对 MPM 产生反应。在这方面,动物研究已经证明了 MPM 对不同免疫疗法的免疫反应性。在 MPM 的情况下,几项临床研究表明,淋巴细胞浸润的存在与更好的预后和针对与肿瘤相关的特定抗原的体液反应之间存在相关性。因此,MPM 的免疫疗法无疑是一种非常有前途但也极具挑战性的治疗方法,它已经突破了免疫系统的防御线。本文回顾了过去和最近的临床策略的发展,这些策略涉及到间皮瘤的免疫治疗。