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Botey-Bataller, J.

Publications and source records attributed to Botey-Bataller, J..

2 recordsLinked to original sources

CellDemux: coherent genetic demultiplexing in single-cell and single-nuclei experiments.

Multiplexed single-cell experiment designs are superior in terms of reduced batch effects, increased cost-effectiveness, throughput and statistical power. However, current computational strategies using genetics to demultiplex single-cell (sc) libraries are limited when applied to single-nuclei (sn) sequencing data (e.g., snATAC-seq and snMultiome). Here, we present CellDemux: a computational framework for genetic demultiplexing within and across data modalities, including single-cell, single-nuclei and paired snMultiome measurements. CellDemux uses a consensus approach, leveraging modality-specific tools to robustly identify non-empty oil droplets and singlets, which are subsequently demultiplexed to donors. Notable, CellDemux demonstrates good performance in demultiplexing snMultiome data and is generalizable to single modalities, i.e. snATAC-seq and sc/snRNA-seq libraries. We benchmark CellDemux on 187 genetically multiplexed libraries from 800 samples (scRNA-seq, snATAC-seq, CITE-seq and snMultiome), confidently identifying and assigning cells to 88% of donors. In paired snMultiome libraries, CellDemux achieves consistent demultiplexing across data modalities. Moreover, analysis of 38 snATAC libraries from 149 samples shows that CellDemux retains more genetically demultiplexed nuclei for downstream analyses compared to existing methods. In summary, CellDemux is a modular and robust framework that deconvolves donors from genetically multiplexed single-cell and single-nuclei RNA/ATAC/Multiome libraries.

genomics↗

MMR vaccination induces a trained immunity program characterized by functional and metabolic reprogramming of γδ T cells

The measles, mumps and rubella (MMR) vaccine protects against all-cause mortality in children, but the immunological mechanisms mediating these effects are poorly known. We systematically investigated whether MMR can induce long-term functional changes in innate immune cells, a process termed trained immunity, that could at least partially mediate this heterologous protection. In a randomized placebo-controlled trial, 39 healthy adults received either the MMR vaccine or a placebo. By using single-cell RNA-sequencing, we found that MMR caused transcriptomic changes in CD14-positive monocytes and NK cells, but most profoundly in {gamma}{delta} T cells. Surprisingly, monocyte function was not altered by MMR vaccination. In contrast, the function of {gamma}{delta} T cells was significantly enhanced by MMR vaccination, with higher production of TNF and IFN{gamma}, as well as upregulation of cellular metabolic pathways. In conclusion, we describe a new trained immunity program characterized by modulation of {gamma}{delta} T cell function induced by MMR vaccination. One-sentence summaryMMR vaccination induces cellular and metabolic reprogramming in {gamma}{delta} T cells towards a more active phenotype.

immunology↗