University of Illinois College of Medicine Peoria, Peoria, Illinois, United States of America.
PLoS One. 2019 Apr 1;14(4):e0214526. doi: 10.1371/journal.pone.0214526. eCollection 2019.
Bloodstream infection (BSI) is the major cause of mortality in acute lymphocytic leukemia (ALL). Causative pathogens in BSI originate from the gut microbiota due to an increase in intestinal permeability, a process known as bacterial translocation (BT). The gut microbiota in physiological conditions is controlled by a large number of immune cells as part of the gut-associated lymphoid tissue (GALT).The aim of the current study was to investigate the mechanism of bacterial translocation in leukemia by identifying and characterizing alterations in the GALT in leukemic mouse model. Our studies revealed a severe impairment of the GALT characterized by a loss of lymphatic cells in ALL, which eventually led to BSI. We identified differentially expressed genes in the intraepithelium and the lamina propria, which may contribute to BT and to the impairment of lymphocyte migration.
血流感染(BSI)是急性淋巴细胞白血病(ALL)患者死亡的主要原因。BSI 的病原体源自肠道微生物群,这是由于肠道通透性增加,即所谓的细菌易位(BT)。在生理条件下,肠道微生物群受大量免疫细胞控制,这些免疫细胞是肠道相关淋巴组织(GALT)的一部分。本研究旨在通过鉴定和描述白血病小鼠模型中 GALT 的改变,来研究白血病中细菌易位的机制。我们的研究揭示了 GALT 的严重损伤,ALL 患者的淋巴样细胞丢失,最终导致 BSI。我们在黏膜上皮内和固有层中鉴定了差异表达的基因,这些基因可能有助于 BT 和淋巴细胞迁移的损伤。