Publications by authors named "Baptiste Robin"

Article Synopsis
  • Aggregation of therapeutic antibodies, specifically under mild temperature stress, significantly influences the immune response by enhancing the activation of CD4 T-cells compared to native antibodies.
  • Large insoluble aggregates of infliximab (IFX) have been shown to recruit more CD4 T-cells and present a broader range of epitopes than the native form.
  • The study reveals that the size and quantity of antibody aggregates produced under mild conditions can modulate monocyte-derived dendritic cell activation and T-cell responses, indicating a dose-dependent relationship.
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Most nanoparticles produced for drug delivery purposes are spherical. However, the literature suggests that elongated particles are advantageous, notably in terms of cellular uptake. Thus, we synthesized biocompatible polylactide-b-poly(ethylene glycol) (PLA-PEG) polymers bearing carboxylate moieties, and used them to formulate worm-like nanoparticles by a simple emulsion-evaporation process.

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COVID-19 is caused by the infection of the lungs by SARS-CoV-2. Monoclonal antibodies, such as sotrovimab, showed great efficiency in neutralizing the virus before its internalization by lung epithelial cells. However, parenteral routes are still the preferred route of administration, even for local infections, which requires injection of high doses of antibody to reach efficacious concentrations in the lungs.

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Tissue engineering aims to restore or replace different types of biological tissues through the association of cells, biologic factors and biomaterials. Currently, stem cells arise as a major cell source for many therapeutic indications, and their association with 3D scaffolds allow increasing regenerative medicine efficiency. In this context, the use of RNA interference to enhance or control stem cell differentiation into the desired phenotype appears as a promising strategy.

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In this study, we proved that the stabilisation of Pickering emulsions by polymer nanoparticles (NPs) heavily depends on polymer characteristics. We prepared NPs with four poly(lactide-co-glycolide) polymers (PLGA), of different molar masses (14,000 and 32,000 g/mol) and end groups (acid or alkylester). NPs were either bare (without stabilising polymer) or covered by polyvinyl alcohol (PVA).

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Article Synopsis
  • The development of anti-drug antibodies (Abs) poses a significant challenge in treating patients with biological products (BPs), influenced by factors like BP aggregates which may trigger immune responses.
  • Aggregates of infliximab, an anti-TNF-α antibody, were found to stimulate maturation of human monocyte-derived dendritic cells (DCs) and enhance T cell proliferation and cytokine production.
  • The study identified that the FcγRIIa receptor and spleen tyrosine kinase (Syk) play crucial roles in the activation of DCs and T cells in response to infliximab aggregates, providing new insights into the immunogenicity of BPs.
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Biocompatible chemical cross-linked hybrid polyethylene glycol-based hydrogels were obtained from a sol-gel process using bis-silylated molecular precursors in biocompatible conditions. This soft procedure (pH = 7.4, at 25 °C), allows the production of microgels by microfluidics and easy encapsulation of a model protein (Bovin Serum Albumine, BSA).

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Pickering emulsions were formulated using biodegradable and biocompatible poly(lactic- co-glycolic acid) (PLGA) nanoparticles (NPs) prepared without surfactants or any other polymer than PLGA. A pharmaceutical and cosmetic oil (Miglyol) was chosen as the oil phase at a ratio of 10% w/w. These emulsions were then compared with emulsions using the same oil but formulated with well-described PLGA-poly(vinyl alcohol) (PVA) NPs, i.

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