Clonal hematopoiesis and inflammation: A review of mechanisms and clinical implications

Daniel I Nathan1, Max Dougherty1, Manasa Bhatta2

  • 1Tisch Cancer Institute, Division of Hematology and Medical Oncology, The Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Insights

Clonal hematopoiesis (CH), driven by mutations in hematopoietic stem cells, is linked to aging and inflammation. Understanding this link may reveal new therapies for myeloid malignancy.

Area of Science:

  • Hematology
  • Immunology
  • Gerontology

Background:

  • Clonal hematopoiesis (CH) involves somatic mutations in hematopoietic stem and progenitor cells (HSPC).
  • CH is associated with aging, increased risk of hematologic malignancy, cardiovascular disease, and inflammatory conditions.
  • The interplay between CH, aging, and inflammation is a growing area of research.

Purpose of the Study:

  • To review the complex relationship between inflammation and CH.
  • To summarize current understanding of how inflammation influences CH and vice versa.
  • To highlight the implications for preventing myeloid malignancy.

Main Methods:

  • This is a review article.
  • Synthesizes findings from observational and experimental studies.
  • Focuses on the pathophysiologic and clinical aspects of the CH-inflammation interaction.

Main Results:

  • CH may be a common factor in age-related inflammatory diseases.
  • Inflammation can promote the development and expansion of CH clones.
  • The bidirectional relationship between CH and inflammation is central to disease pathogenesis.

Conclusions:

  • The relationship between inflammation and CH is critical for understanding aging-related diseases.
  • Targeting this relationship may offer therapeutic strategies to prevent myeloid malignancy progression.
  • Further research is needed to fully elucidate these complex interactions.

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