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Asger Jakobsen
BMBCh, MRCP, DPhil
Postdoctoral Clinical Research Fellow
Research groups
I studied medical sciences at the University of Cambridge, and qualified in clinical medicine from Oxford Medical School in 2014. I am currently working as a Postdoctoral Clinical Research Fellow in the MRC Molecular Haematology Unit supervised by Prof Paresh Vyas.
My research focuses on how mutations affecting epigenetic regulators lead to clonal expansion in haematopoietic stem and progenitor cells. Proteins that control DNA methylation, such as DNMT3A and TET2, are important in stem cell differentiation and regulating how genes are expressed. Mutations in these genes are commonly found in blood cells of healthy older people, lead to clonal expansion, and are associated with increased risk of developing blood cancers, such as acute myeloid leukaemia (AML), and other adverse outcomes.
In collaboration with surgical teams at NDORMS and the Nuffield Orthopaedic Centre, I established the MARCH Study to collect bone marrow and blood samples from individuals undergoing hip replacement surgery. This has made it possible to study clonal haematopoiesis in healthy older individuals, where samples are otherwise difficult to obtain.
We have developed single-cell methods for analysing genotype along with gene expression and epigenetic readouts, and are using these to study the consequences of mutations on blood stem and progenitor cells. Through this work, we hope to gain a better understanding of how age-related clones are selected and identify a basis for rational therapeutic targeting to reduce the risk of leukaemia and other diseases.
Key publications
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Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging.
Journal article
Jakobsen NA. et al, (2024), Cell Stem Cell, 31, 1127 - 1144.e17
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GTAC enables parallel genotyping of multiple genomic loci with chromatin accessibility profiling in single cells.
Journal article
Turkalj S. et al, (2023), Cell Stem Cell, 30, 722 - 740.e11
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A hematopoietic stem cell subset that retains memory of prior inflammatory stress accumulates in aging and clonal hematopoiesis
Preprint
Zeng AGX. et al, (2023)
Recent publications
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Supplementary Protocol from A phase Ib/II study of ivosidenib with venetoclax +/- azacitidine in IDH1-mutated myeloid malignancies
Other
Lachowiez CA. et al, (2024)
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Supplementary Protocol from A phase Ib/II study of ivosidenib with venetoclax +/- azacitidine in IDH1-mutated myeloid malignancies
Other
Lachowiez CA. et al, (2024)
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Supplementary Tables and Figures from A phase Ib/II study of ivosidenib with venetoclax +/- azacitidine in IDH1-mutated myeloid malignancies
Other
Lachowiez CA. et al, (2024)
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Supplementary Tables and Figures from A phase Ib/II study of ivosidenib with venetoclax +/- azacitidine in IDH1-mutated myeloid malignancies
Other
Lachowiez CA. et al, (2024)
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Risk Stratification in Older Intensively Treated Patients With AML.
Journal article
Versluis J. et al, (2024), J Clin Oncol