Takata So, Koh Genju, Han Yuki, Yoshida Hiroko, Shiroyama Takayuki, Takada Hiromune, Masuhiro Kentarou, Nasu Shingo, Morita Satomu, Tanaka Ayako, Hashimoto Syouji, Uriu Kiyoaki, Suzuki Hidekazu, Tamura Yoshitaka, Okamoto Norio, Nagai Takayuki, Hirashima Tomonori
Department of Thoracic Oncology, Osaka Prefectural Hospital Organization Osaka Habikino Medical Center, 3-7-1, Habikino, Habikino City, Osaka, 583-8588, Japan.
Department of Medical Oncology, Yao Tokushukai General Hospital, 1-17, Wakakusa Town, Yao City, Osaka, 581-0011, Japan.
J Infect Chemother. 2019 Jan;25(1):54-58. doi: 10.1016/j.jiac.2018.06.016. Epub 2018 Jul 25.
Anti-programmed cell death-1 (PD-1) agents enhance the antitumor immunoresponse. A number of reports have indicated that patients with malignancies who receive anti-PD-1 agents are at risk for tuberculosis (TB) infection. In this report, we present a patient with non-small cell lung cancer who developed pulmonary tuberculosis while receiving the anti-PD-1 agent nivolumab, and who subsequently demonstrated a paradoxical response (PR) 10 days after initiation of anti-MTB treatment. We suggest that anti-PD-1 agents not only induce the development of pulmonary TB, but also development of PR after anti-MTB treatment, through upregulation of the immune response. Furthermore, based on their radiological and immunological similarity, we speculate that the schema of development of PR closely resembles that of pseudoprogression in non-small cell lung cancer patients after anti-PD-1 treatment.
抗程序性细胞死亡蛋白1(PD-1)药物可增强抗肿瘤免疫反应。多项报告表明,接受抗PD-1药物治疗的恶性肿瘤患者有感染结核病(TB)的风险。在本报告中,我们介绍了一名非小细胞肺癌患者,该患者在接受抗PD-1药物纳武单抗治疗期间发生了肺结核,并在开始抗结核治疗10天后出现了矛盾反应(PR)。我们认为,抗PD-1药物不仅会诱发肺结核的发生,还会通过上调免疫反应在抗结核治疗后引发矛盾反应。此外,基于其影像学和免疫学相似性,我们推测矛盾反应的发生机制与非小细胞肺癌患者接受抗PD-1治疗后的假性进展非常相似。