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. 2022 Jul;8(7):e09887.
doi: 10.1016/j.heliyon.2022.e09887. Epub 2022 Jul 6.

Examining the interactions of Galahad™ compound with viruses to develop a novel inactivated influenza A virus vaccine

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Free PMC article

Examining the interactions of Galahad™ compound with viruses to develop a novel inactivated influenza A virus vaccine

Dale L Barnard et al. Heliyon. 2022 Jul.
Free PMC article

Abstract

Galahad™ is a proanthocyanidin complexed with polysaccharides that inactivates viruses and indicates potential for an innovative approach to making protective vaccines. The polysaccharide portion of Galahad™ consists mainly of arabinan and arabinogalactan. In a seven-day toxicity study in rats, it was not toxic even when tested undiluted. Galahad™ inactivated a wide range of DNA and RNA viruses including adenoviruses, corona viruses such as SARS-CoV-2, and influenza viruses. Electron microscopy studies showed that exposure to Galahad™ caused extensive clumping of virions followed by lack of detection of virions after longer periods of exposure. Based on the viral inactivation data, the hypotheses tested is that Galahad™ inactivation of virus can be used to formulate a protective inactivated virus vaccine. To evaluate this hypothesis, infectious influenza A virus (H5N1, Duck/MN/1525/81) with a titer of 105.7 CCID50/0.1 ml was exposed for 10 min to Galahad™. This treatment caused the infectious virus titer to be reduced to below detectable limits. The Galahad™ -inactivated influenza preparation without adjuvant or preservative was given to BALB/c mice using a variety of routes of administration and dosing regimens. The most protective route of administration and dosing regimen was when mice were given the vaccine twice intranasally, the second dose coming 14 days after the primary vaccine dose. All the mice receiving this vaccine regimen survived the virus challenge while only 20% of the mice receiving placebo survived. This suggests that a Galahad™-inactivated influenza virus vaccine can elicit a protective immune response even without the use of an adjuvant. This technology should be investigated further for its potential to make effective human vaccines.

Keywords: Catechin; H5N1; Influenza; Polysaccharide; SARS-CoV-2 (COVID-19); Vaccine.

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Conflict of interest statement

The authors declare the following conflict of interests: Thomas Konowalchuk owns shares of Galaxy Force Technologies, LLC that has patent rights to produce vaccines using GalahadTM. The other authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. Research on GalahadTM did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors, but was financed by companies with ownership interest in GalahadTM without role in experimental design, data analysis, collection and interpretation.

References

    1. Phytother Res. 2020 Feb;34(2):239-253 - PubMed
    1. J Biol Chem. 2011 Oct 21;286(42):36198-214 - PubMed
    1. Antivir Chem Chemother. 2007;18(3):125-32 - PubMed
    1. J Virol. 1999 Oct;73(10):8303-7 - PubMed
    1. Medicine (Baltimore). 2016 Aug;95(33):e4247 - PubMed

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