Publications by authors named "Anucha Preechanukul"

Natural killer (NK) cells are innate lymphocytes that can rapidly mount a response to their targets by employing diverse mechanisms. Due to their functional attributes, NK cells have been implicated in anti-viral and anti-tumour immune responses. Although traditionally known to mount non-specific, rapid immune responses, in recent years, the notion of memory NK cells with adaptive features has gained more recognition.

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Article Synopsis
  • The study explores the metabolic requirements of natural killer (NK) cells with a focus on their memory-like differentiation in response to bacterial infections, particularly melioidosis caused by Gram-negative bacteria.
  • Researchers used a specific NK cell memory assay to analyze how BP (the bacteria responsible for melioidosis) stimulates metabolism in recovered patients, noting key changes in transporter expression and metabolic pathways.
  • Findings suggest a significant role of oxidative phosphorylation and fatty acid oxidation in the formation and function of memory-like NK cells, highlighting potential implications for vaccine development and infection monitoring.
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NK cells are endowed with immunological memory to a range of pathogens but the development of NK cell memory in bacterial infections remains elusive. Here, we establish an assay inducing memory-like NK cell response to , the causative agent of the severe bacterial disease called melioidosis, and explore NK cell memory in a melioidosis patient cohort. We show that NK cells require bacteria-primed monocytes to acquire memory-like properties, demonstrated by bacteria-specific responses, features that strongly associate with CD160 expression.

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Sepsis is a complex heterogeneous condition, and the current lack of effective risk and outcome predictors hinders the improvement of its management. Using a reductionist approach leveraging publicly available transcriptomic data, we describe a knowledge gap for the role of ACVR1B (activin A receptor type 1B) in sepsis. ACVR1B, a member of the transforming growth factor-beta (TGF-beta) superfamily, was selected based on the following: 1) induction upon exposure of neutrophils from healthy subjects with the serum of septic patients (GSE49755), and 2) absence or minimal overlap between ACVR1B, sepsis, inflammation, or neutrophil in published literature.

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Article Synopsis
  • Burkholderia pseudomallei is a bacterium that causes melioidosis and can create multinucleated giant cells (MNGCs) in lab settings, but its genetic variations and how they relate to plaque formation are not well understood.
  • A study screened 52 clinical and 11 environmental isolates of B. pseudomallei, revealing that most could induce plaque formation in some cell lines, except for one environmental strain and one morphotype that showed impaired growth and MNGC formation.
  • Genomic analysis indicated that the isolates lacking plaque formation had significant gene loss on chromosome 2, suggesting that genetic differences among environmental isolates may impact their potential to cause clinical infections.
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