Trowbridge Jennifer J, Starczynowski Daniel T
The Jackson Laboratory, Bar Harbor, ME.
Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
J Exp Med. 2021 Jul 5;218(7). doi: 10.1084/jem.20201544. Epub 2021 Jun 15.
With a growing aged population, there is an imminent need to develop new therapeutic strategies to ameliorate disorders of hematopoietic aging, including clonal hematopoiesis and myelodysplastic syndrome (MDS). Cell-intrinsic dysregulation of innate immune- and inflammatory-related pathways as well as systemic inflammation have been implicated in hematopoietic defects associated with aging, clonal hematopoiesis, and MDS. Here, we review and discuss the role of dysregulated innate immune and inflammatory signaling that contribute to the competitive advantage and clonal dominance of preleukemic and MDS-derived hematopoietic cells. We also propose how emerging concepts will further reveal critical biology and novel therapeutic opportunities.
随着老年人口的不断增加,迫切需要开发新的治疗策略来改善造血衰老相关疾病,包括克隆性造血和骨髓增生异常综合征(MDS)。先天免疫和炎症相关通路的细胞内在失调以及全身炎症与衰老、克隆性造血和MDS相关的造血缺陷有关。在这里,我们回顾并讨论失调的先天免疫和炎症信号在白血病前期和MDS来源的造血细胞的竞争优势和克隆优势中所起的作用。我们还提出新兴概念将如何进一步揭示关键生物学特性和新的治疗机会。