Speletas Matthaios, Vyzantiadis Timoleon-Achilleas, Kalala Fani, Plastiras Dimitrios, Kokoviadou Kyriaki, Antoniadis Antonios, Korantzis Ioannis
Department of Immunology and Histocompatibility, University of Thessaly Medical School, Larissa, Greece.
Med Mycol. 2008 May;46(3):259-63. doi: 10.1080/13693780701558969.
In this report we describe a patient suffering from chronic myeloid leukemia (CML), who was treated for 4.5 years with imatinib and developed pneumonia caused by two Candida species, i.e., C. krusei and C. glabrata. The patient was in complete hematologic remission and molecular analyses did not display the presence of TLR2-R752Q, TLR4-D299G and TLR4-T399I polymorphisms that may predispose individuals to fungal infections. This case report indicates that in some patients, as previously observed, the long-term administration of targeted therapy might affect immunity and predispose patients to opportunistic and life-threatening fungal infections.
在本报告中,我们描述了一名患有慢性粒细胞白血病(CML)的患者,该患者接受伊马替尼治疗4.5年,并发由两种念珠菌,即克鲁斯念珠菌和光滑念珠菌引起的肺炎。该患者处于完全血液学缓解状态,分子分析未显示可能使个体易患真菌感染的TLR2-R752Q、TLR4-D299G和TLR4-T399I多态性的存在。本病例报告表明,正如之前所观察到的,在一些患者中,长期使用靶向治疗可能会影响免疫力,使患者易患机会性和危及生命的真菌感染。