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Mariëlle C. Haks

Researcher at Leiden University Medical Center

Publications -  42
Citations -  1241

Mariëlle C. Haks is an academic researcher from Leiden University Medical Center. The author has contributed to research in topics: Tuberculosis & Immune system. The author has an hindex of 17, co-authored 42 publications receiving 887 citations. Previous affiliations of Mariëlle C. Haks include Maastricht University.

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The DNA Damage-Regulated Autophagy Modulator DRAM1 Links Mycobacterial Recognition via TLR-MYD88 to Autophagic Defense

TL;DR: Analysis in zebrafish and human macrophage models of mycobacterial infection reveals that the DNA damage-regulated autophagy modulator DRAM1 functions downstream of pathogen recognition by the Toll-like receptor (TLR)/interleukin-1 receptor (IL1R)-MYD88-NF-κB innate immune sensing pathway to activate selective Autophagy.
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Identification of biomarkers for tuberculosis disease using a novel dual-color RT-MLPA assay

TL;DR: To identify/monitor multi-component host biomarker signatures at the transcriptomic level in large human cohort studies, a dual-color reverse-transcriptase multiplex ligation-dependent probe amplification (dcRT–MLPA) method is developed and validated, permitting rapid and accurate expression profiling of as many as 60–80 transcripts in a single reaction.
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Human CD8+ T-cells recognizing peptides from Mycobacterium tuberculosis (Mtb) presented by HLA-E have an unorthodox Th2-like, multifunctional, Mtb inhibitory phenotype and represent a novel human T-cell subset.

TL;DR: These results identify a novel human T-cell subset with an unorthodox, multifunctional Th2 like phenotype and cytolytic or regulatory capacities, involved in the human immune response to mycobacteria and demonstrable in active TB patients’ blood.
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Longitudinal Immune Responses and Gene Expression Profiles in Type 1 Leprosy Reactions

TL;DR: Investigation of the longitudinal host response of a leprosy patient, who was affected by a type 1 reaction (T1R) after MDT-treatment, shows that increased inflammation, vasculoneogenesis and cytotoxicity, perturbed T-cell regulation as well as IFN-induced genes play an important role in T1R and provide potential T1r-specific host biomarkers.