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Inflammageing and clonal haematopoiesis interplay and their impact on human disease.

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Nature reviews. Molecular cell biology 2026 Vol.27(5) p. 377-393 cited 4 OA Hematopoietic Stem Cell Transplantat
TL;DR Findings in preclinical and partly in clinical studies indicate that nutrient-based interventions target complementary cancer cachexia alterations, and it is likely that combinatorial approaches, integrating several specific nutrients, will provide an effective base for managing cancer patients during the long journey of the disease.
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PubMed DOI PMC OpenAlex Semantic 마지막 보강 2026-04-29
OpenAlex 토픽 · Hematopoietic Stem Cell Transplantation Acute Myeloid Leukemia Research Zebrafish Biomedical Research Applications

Hajishengallis G, Chavakis T

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Findings in preclinical and partly in clinical studies indicate that nutrient-based interventions target complementary cancer cachexia alterations, and it is likely that combinatorial approaches, inte

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APA George Hajishengallis, T Chavakis (2026). Inflammageing and clonal haematopoiesis interplay and their impact on human disease.. Nature reviews. Molecular cell biology, 27(5), 377-393. https://doi.org/10.1038/s41580-025-00936-y
MLA George Hajishengallis, et al.. "Inflammageing and clonal haematopoiesis interplay and their impact on human disease.." Nature reviews. Molecular cell biology, vol. 27, no. 5, 2026, pp. 377-393.
PMID 41491423

Abstract

Clonal haematopoiesis of indeterminate potential (CHIP) is an ageing-related condition associated with a substantial fraction of circulating leukocytes having descended from a single somatically mutated haematopoietic stem cell (HSC). CHIP increases the risk of haematological malignancies and several chronic diseases (for example, cardiovascular pathologies) and contributes to persistent, low-grade inflammation or inflammageing. Inflammageing, in turn, promotes functional impairment of normal HSCs, including reduced self-renewal potential. By contrast, CHIP-mutant HSCs not only are resistant to inflammageing-induced functional decline but also gain a selective expansion advantage in an inflammatory environment. A recent surge of discoveries has increased our understanding of the CHIP-inflammageing interplay, from a mechanistic and clinical perspective, highlighting its broader relevance to age-related diseases. In this Review, we discuss the molecular and cellular mechanisms that cause CHIP, its interplay with inflammageing, as well as the pathophysiological consequences and the translational implications for diseases that affect older individuals.

MeSH Terms

Humans; Clonal Hematopoiesis; Inflammation; Hematopoietic Stem Cells; Aging; Animals; Hematopoiesis; Hematologic Neoplasms