New York, July 31: Scientists have developed a new nanoparticle vaccine that could effectively protect mice against influenza A virus, providing a promising approach for developing universal vaccines for the infectious disease.
The double-layered vaccine made with peptides, which are compounds consisting of two or more amino acids linked in a chain, showed strong potential for combating influenza viruses.
The nanoparticles, delivered by skin vaccination with a dissolvable microneedle patch, mimic the biological cues of viruses and initiate danger signals that activate immune responses, the Xinhua reported.
The microneedle patch is syringe-free, painless, thermostable and self-applicable, said Wang Baozhong, Associate Professor at Georgia State University in the US.
Each double-layered nanoparticle has a core made of peptides from nucleoprotein (NP) — an internal influenza protein that has been found to produce cross-protection against influenza virus by inducing T-cell immune responses.
The nanoparticle also has an outside coating made of four peptides from the ectodomain of the influenza A M2 protein (M2e), a promising target for universal flu vaccines. The M2e sequences came from human, swine and avian influenza strains.
In the paper published in the Proceedings of the National Academy of Sciences, the team found that mice which received the nanoparticle vaccines completely survived various influenza A virus exposures while all mice that received a placebo died within one week.
“The adaptive immune system includes B lymphocytes mediating antibody responses and T lymphocytes mediating cellular responses,” Baozhong said.
“Our novel nanoparticles trigger immune responses of both immune branches. We have seen the synergistic role of the two branches in providing broad cross-protection against a wide range of diverse influenza virus challenges after vaccination with these layered peptide nanoparticles,” he added. This vaccine approach could also be used to develop vaccines for other pathogens and cancers, Wang said. (IANS)