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From an in vivo to an in vitro relative potency (IVRP) assay to fully characterize a multicomponent O-antigen based vaccine against Shigella. | LitMetric

AI Article Synopsis

  • Outer membrane vesicles (OMV), particularly those from engineered Gram-negative bacteria called Generalized Modules for Membrane Antigens (GMMA), are being developed as a platform for new polysaccharide vaccines targeting Shigella.
  • The altSonflex1-2-3 vaccine targets multiple O-Antigens associated with Shigella serotypes to provide broad protection, especially for children in low-middle income countries.
  • Researchers developed an in vitro potency assay that can replace animal testing, enabling better detection of vaccine effectiveness while minimizing variability, and their methods can be extended to improve other O-Antigen based vaccines.

Article Abstract

Outer membrane vesicles (OMV) represent an innovative platform for the design of polysaccharide based vaccines. Generalized Modules for Membrane Antigens (GMMA), OMV released from engineered Gram-negative bacteria, have been proposed for the delivery of the O-Antigen, key target for protective immunity against several pathogens including Shigella. altSonflex1-2-3 is a GMMA based vaccine, including S. sonnei and S. flexneri 1b, 2a and 3a O-Antigens, with the aim to elicit broad protection against the most prevalent Shigella serotypes, especially affecting children in low-middle income countries. Here we developed an In Vitro Relative Potency assay, based on recognition of O-Antigen by functional monoclonal antibodies selected to bind the key epitopes of the different O-Antigen active ingredients, directly applied to our Alhydrogel-formulated vaccine. Heat-stressed altSonflex1-2-3 formulations were generated and extensively characterized. The impact of detected biochemical changes in in vivo and in vitro potency assays was assessed. The overall results showed how the in vitro assay can replace the use of animals, overcoming the inherently high variability of in vivo potency studies. The entire panel of physico-chemical methods developed will contribute to detect suboptimal batches and will be valuable to perform stability studies. The work on Shigella vaccine candidate can be easily extended to other O-Antigen based vaccines.

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Source
http://dx.doi.org/10.1016/j.carbpol.2023.120920DOI Listing

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