Koya Toshiyuki, Tsubata Chikako, Kagamu Hiroshi, Koyama Ken-ichi, Hayashi Masachika, Kuwabara Katsuhiro, Itoh Takui, Tanabe Yoshinari, Takada Toshinori, Gejyo Fumitake
Department of Homeostatic Regulation and Development, Graduate School of Medical and Dental Sciences, Niigata University, and Nishi-Niigata Chuo National Hospital, Niigata, Japan.
J Infect Chemother. 2009 Apr;15(2):118-22. doi: 10.1007/s10156-008-0662-8. Epub 2009 Apr 25.
We report the case of a 44-year-old woman with disseminated Mycobacterium avium complex (MAC) infection involving multiple bone lesions despite a normal healthy status until 6 months previously. Because she was suspected to have acquired immunodeficiency, we tested interferon (IFN)-gamma production by peripheral blood mononuclear cells (PBMC) after phytohemagglutinin (PHA) or anti-CD3 stimulation, and found that these cells produced no, or undetectable, levels of IFN-gamma in the presence of the patient's plasma, but produced nearly normal levels of IFN-gamma in the presence of healthy donor plasma. Since the IgG fraction of the patient's plasma was capable of blocking in vitro responses to IFN-gamma, the cause of disseminated MAC infection in this case appeared to be anti-IFN-gamma autoantibodies. To reduce the titer of anti-IFN-gamma autoantibodies, the patient received intravenous immunoglobulin (IVIG). However, titer of autoantibodies changed little compared to that before IVIG administration. According to our literature search, this is only the second case of disseminated MAC infection associated with anti-IFN-gamma autoantibodies in Japan.
我们报告了一例44岁女性患者的病例,该患者患有播散性鸟分枝杆菌复合体(MAC)感染,累及多处骨病变,而在此之前6个月她的健康状况一直正常。由于怀疑她患有获得性免疫缺陷,我们检测了植物血凝素(PHA)或抗CD3刺激后外周血单个核细胞(PBMC)产生干扰素(IFN)-γ的情况,发现这些细胞在患者血浆存在的情况下不产生或产生无法检测到的IFN-γ水平,但在健康供体血浆存在的情况下产生接近正常水平的IFN-γ。由于患者血浆的IgG部分能够阻断体外对IFN-γ的反应,因此该病例中播散性MAC感染的原因似乎是抗IFN-γ自身抗体。为了降低抗IFN-γ自身抗体的滴度,患者接受了静脉注射免疫球蛋白(IVIG)。然而,与IVIG给药前相比,自身抗体滴度变化不大。根据我们的文献检索,这是日本第二例与抗IFN-γ自身抗体相关的播散性MAC感染病例。