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A Live Probiotic Vaccine Prototype Based on Conserved Influenza a Virus Antigens Protect Mice against Lethal Influenza Virus Infection. | LitMetric

AI Article Synopsis

  • Researchers are exploring the use of the L3 bacterial vector as a novel oral vaccine platform to induce immune responses against the influenza virus.
  • Two vaccine prototypes were developed by modifying the L3 strain to express specific viral proteins, and their effectiveness was tested in mice.
  • The results showed one prototype provided full protection against lethal influenza challenges, suggesting its potential as a promising candidate for further development in preventing influenza.

Article Abstract

Background: Due to the highly variable nature of the antigenic properties of the influenza virus, many efforts have been made to develop broadly reactive influenza vaccines. Various vaccine platforms have been explored to deliver conserved viral antigens to the target cells to induce cross-reactive immune responses. Here, we assessed the feasibility of using L3 as a bacterial vector for oral immunization against influenza virus.

Methods: we generated two vaccine prototypes by inserting full-length HA2 (L3-HA2) protein or its long alpha helix (LAH) domain in combination with four M2e tandem repeats (L3-LAH+M2e) into genome of L3 probiotic strain. The immunogenicity and protective potential of these oral vaccines were assessed in a lethal challenge model in BALB/c mice.

Results: as expected, both vaccine prototypes induced HA stem-targeting antibodies, whereas only L3-LAH+4M2e vaccine induced M2e-specific antibody. The L3-HA2 vaccine partially protected mice against lethal challenge with two H1N1 heterologous viruses, while 100% of animals in the L3-LAH+4M2e vaccine group survived in both challenge experiments, and there was significant protection against weight loss in this group, compared to the L3 vector-immunized control mice.

Conclusions: the recombinant enterococcal strain L3-LAH+4M2e can be considered as a promising live probiotic vaccine candidate for influenza prevention and warrants further evaluation in relevant pre-clinical models.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615285PMC
http://dx.doi.org/10.3390/biomedicines9111515DOI Listing

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