Pagani Ilaria S, Poudel Govinda, Wardill Hannah R
Cancer Program, Precision Medicine Theme, South Australian Health & Medical Research Institute, Adelaide 5000, Australia.
Faculty of Health and Medical Sciences, School of Medicine, University of Adelaide, Adelaide 5000, Australia.
Microorganisms. 2022 Mar 25;10(4):713. doi: 10.3390/microorganisms10040713.
Despite significant advances in the treatment of Chronic Myeloid and Acute Lymphoblastic Leukaemia (CML and ALL, respectively), disease progression and relapse remain a major problem. Growing evidence indicates the loss of immune surveillance of residual leukaemic cells as one of the main contributors to disease recurrence and relapse. More recently, there was an appreciation for how the host's gut microbiota predisposes to relapse given its potent immunomodulatory capacity. This is especially compelling in haematological malignancies where changes in the gut microbiota have been identified after treatment, persisting in some patients for years after the completion of treatment. In this hypothesis-generating review, we discuss the interaction between the gut microbiota and treatment responses, and its capacity to influence the risk of relapse in both CML and ALL We hypothesize that the gut microbiota contributes to the creation of an immunosuppressive microenvironment, which promotes tumour progression and relapse.
尽管在慢性髓性白血病和急性淋巴细胞白血病(分别为CML和ALL)的治疗方面取得了重大进展,但疾病进展和复发仍然是一个主要问题。越来越多的证据表明,对残留白血病细胞的免疫监视丧失是疾病复发的主要原因之一。最近,鉴于宿主肠道微生物群具有强大的免疫调节能力,人们开始认识到它如何导致复发。这在血液系统恶性肿瘤中尤其引人注目,因为在治疗后已发现肠道微生物群发生了变化,在一些患者中,这种变化在治疗结束后持续数年。在这篇提出假设的综述中,我们讨论了肠道微生物群与治疗反应之间的相互作用,以及它影响CML和ALL复发风险的能力。我们假设肠道微生物群有助于创造一个免疫抑制微环境,从而促进肿瘤进展和复发。