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Tartour, E.

Publications and source records attributed to Tartour, E..

2 recordsLinked to original sources

A new spatial multi-omics approach to deeply characterize human cancer tissue using a single tissue section

In the ever-changing world of digital pathology, being able to extract a maximum amount of information from a patient tissue sample is of paramount importance for better diagnosis, disease characterization, and therapeutic strategies. Recent technologies such as multiplex immunofluorescence imaging and spatial transcriptomic now enable a deep analysis of protein and gene expression while retaining the spatial context of the tissue. Here, we describe an innovative approach combining a 34-protein Phenocycler panel and transcriptome analysis using Visium on a single head and neck squamous cell carcinoma section. While protein analysis reveals the complexity of the immune phenotypes involved in the disease, transcriptome analysis reveals the intricate cellular states of cancer cells that coexist within the patients tumor. Finally, integrating both omics modalities, we uncover unique comparison of gene and protein expression of spatially resolved cellular subspaces.

cancer biology↗

A synthetic delivery vector for mucosal vaccination

The success of mRNA-based vaccines during the Covid-19 pandemic has highlighted the value of this new platform for vaccine development against infectious disease. However, the CD8+ T cell response remains modest with mRNA vaccines, and these do not induce mucosal immunity, which would be needed to prevent viral spread in the healthy population. To address this drawback, we developed a dendritic cell targeting mucosal vaccination vector, the homopentameric STxB. Here, we describe the highly efficient chemical synthesis of the protein, and its in vitro folding. This straightforward preparation led to a synthetic delivery tool whose biophysical and intracellular trafficking characteristics were largely indistinguishable from recombinant STxB. The chemical approach allowed for the generation of new variants with bioorthogonal handles. Selected variants were chemically coupled to several types of antigens derived from the mucosal viruses SARS-CoV-2 and type 16 human papillomavirus. Upon intranasal administration in mice, mucosal immunity, including resident memory CD8+ T cells and IgA antibodies was induced against these antigens. Our study thereby identifies a novel synthetic antigen delivery tool for mucosal vaccination with an unmatched potential to respond to an urgent medical need.

biochemistry↗