| Literature DB >> 33651967 |
Nobunao Ikewaki1,2, Masaru Iwasaki3, Gene Kurosawa4, Kosagi-Sharaf Rao5, Johant Lakey-Beitia5, Senthilkumar Preethy6, Samuel Jk Abraham6,7,8,9,10.
Abstract
Conventional vaccines to combat COVID-19 through different approaches are at various stages of development. The complexity of COVID-19 such as the potential mutations of the virus leading to antigenic drift and the uncertainty on the duration of the immunity induced by the vaccine have hampered the efforts to control the COVID-19 pandemic. Thus, we suggest an alternative interim treatment strategy based on biological response modifier glucans such as the Aureobasidium pullulans AFO-202-derived β-glucan, which has been reported to induce trained immunity, akin to that induced by the Bacille Calmette-Guérin vaccine, by epigenetic modifications at the central level in the bone marrow. These β-glucans act as pathogen-associated molecular patterns, activating mucosal immunity by binding with specific pathogen recognition receptors such as dectin-1 and inducing both the adaptive and innate immunity by reaching distant lymphoid organs. β-Glucans have also been used as immune adjuvants for vaccines such as the influenza vaccine. Therefore, until a conventional vaccine is widely available, an orally consumable vaccine adjuvant that acts like biosimilars, termed as the wide-spectrum immune-balancing food-supplement-based enteric (β-WIFE) vaccine adjuvant approach, with well-reported safety is worth in-depth investigation and can be considered for a clinical trial.Entities:
Keywords: AFO-202 Beta glucan; Covid-19; immune enhancement; trained Immunity; vaccine adjuvant
Year: 2021 PMID: 33651967 PMCID: PMC7938654 DOI: 10.1080/21645515.2021.1880210
Source DB: PubMed Journal: Hum Vaccin Immunother ISSN: 2164-5515 Impact factor: 3.452