Improved OMV vaccine against Neisseria meningitidis using genetically engineered strains and a detergent-free purification process |
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Authors: | Bas van de Waterbeemd,Mathieu Streefland,Peter van der Ley,Bert Zomer,Harry van Dijken,Dirk Martens,René Wijffels,Leo van der Pol |
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Affiliation: | 1. Netherlands Vaccine Institute, Unit Research and Development, The Netherlands;2. Wageningen University, Bioprocess Engineering, The Netherlands |
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Abstract: | The use of detergent-extracted outer membrane vesicles (OMVs) is an established approach for development of a multivalent PorA vaccine against N. meningitidis serogroup B. Selective removal of lipopolysaccharide (LPS) decreases toxicity, but promotes aggregation and narrows the immune response. Detergent-free OMV vaccines retain all LPS, which preserves the native vesicle structure, but result in high toxicity and lower yield. The present study assessed the effects of gene mutations that attenuated LPS toxicity (lpxL1) or improved OMV yield (rmpM) in combination with the available OMV purification processes. The results substantiate that OMVs from a strain with both mutations, produced with a detergent-free process provide better vaccine characteristics than the traditional detergent-based approach. With comparable toxicity and yield, no aggregation and cross-protection against other PorA subtypes, these OMV vaccines are potentially safe and effective for parenteral use in humans. |
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Keywords: | OMV, outer membrane vesicles (in general) dOMV, detergent OMVs made with combined detergent/EDTA extraction nOMV, native OMVs made with EDTA extraction (without detergent) sOMV, spontaneously released OMVs purified from the culture supernatant dOMV process, purification process for detergent-extracted OMVs dOMV vaccine, OMV vaccine produced with the dOMV process ΔR-dOMV, dOMV vaccine from a specific bacterial strain (in this case the ΔR strain) LPS, lipopolysaccharide PL, phospholipid DOC, deoxycholate EDTA, ethylenediaminetetraacetic acid |
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