Koizumi Yusuke, Sakagami Takuro, Nishiyama Naoya, Hirai Jun, Hayashi Yuta, Asai Nobuhiro, Yamagishi Yuka, Kato Hideo, Hagihara Mao, Sakanashi Daisuke, Suematsu Hiroyuki, Ogawa Kenji, Mikamo Hiroshige
Department of Clinical Infectious Diseases, Aichi Medical University Hospital, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Department of Infection Control and Prevention, Aichi Medical University Hospital, Aichi, Japan.
J Clin Immunol. 2017 Oct;37(7):644-649. doi: 10.1007/s10875-017-0425-3. Epub 2017 Aug 5.
A 67-year-old Japanese female with back pain and severe cachexia visited our hospital. The diagnosis was disseminated Mycobacterium avium complex infection (dMAC) with multiple bone involvement. Anti-mycobacterial chemotherapy was started, but fever persisted and dislocation of cervical vertebrae has made her bedridden. Because anti-interferon (IFN)-γ autoantibody was positive, four doses of rituximab 375 mg/m, every 7 day, were administered. Soon after treatment, progression of osteolytic lesions and wasting has stopped. We proved that rituximab has recovered IFN-γ signaling as shown by IFN-γ-induced STAT1 phosphorylation. It can be a promising option for dMAC cases with anti-IFN-γ autoantibody.
一名67岁的日本女性因背痛和严重恶病质前来我院就诊。诊断为播散性鸟分枝杆菌复合群感染(dMAC),伴有多骨受累。开始抗分枝杆菌化疗,但发热持续,颈椎脱位导致她卧床不起。由于抗干扰素(IFN)-γ自身抗体呈阳性,每7天给予4剂利妥昔单抗,剂量为375mg/m²。治疗后不久,溶骨性病变和消瘦的进展停止。我们证明,利妥昔单抗恢复了IFN-γ信号传导,如IFN-γ诱导的STAT1磷酸化所示。对于伴有抗IFN-γ自身抗体的dMAC病例,它可能是一个有前景的选择。