Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.

Although vaccine delivery through the oral route remains the most convenient and safest way for mass immunization purposes, this method is limited by the requirement for large antigen doses and low vaccine efficacy. In this study, we generated recombinant baculoviruses (rBVs) expressing influenza he...

Full description

Bibliographic Details
Main Authors: Swarnendu Basak, Hae-Ji Kang, Su-Hwa Lee, Ki-Back Chu, Eun-Kyung Moon, Fu-Shi Quan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0233520
id doaj-c990545c91444132a659d6640f2d6cd5
record_format Article
spelling doaj-c990545c91444132a659d6640f2d6cd52021-03-03T21:48:19ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01155e023352010.1371/journal.pone.0233520Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.Swarnendu BasakHae-Ji KangSu-Hwa LeeKi-Back ChuEun-Kyung MoonFu-Shi QuanAlthough vaccine delivery through the oral route remains the most convenient and safest way for mass immunization purposes, this method is limited by the requirement for large antigen doses and low vaccine efficacy. In this study, we generated recombinant baculoviruses (rBVs) expressing influenza hemagglutinin (A/PR/8/34) and orally delivered a low dose of rBVs to evaluate its vaccine efficacy in mice. Intranasal rBV vaccination was included in the whole experiment for comparison. We found that oral vaccination elicited high levels of virus-specific IgG and IgA antibody responses in both serum and mucosal samples (lung, tracheal, intestinal, fecal and vaginal). Surprisingly, complete protection from the lethal influenza challenge was observed, as indicated by reductions in the virus titer, inflammatory cytokine production, body weight change, and enhanced survival. These results suggest that oral delivery of the influenza rBV vaccine induces mucosal and systemic immunity, which protect mice from the lethal influenza virus challenge. Oral delivery of baculovirus vaccines can be developed as an effective vaccination route.https://doi.org/10.1371/journal.pone.0233520
collection DOAJ
language English
format Article
sources DOAJ
author Swarnendu Basak
Hae-Ji Kang
Su-Hwa Lee
Ki-Back Chu
Eun-Kyung Moon
Fu-Shi Quan
spellingShingle Swarnendu Basak
Hae-Ji Kang
Su-Hwa Lee
Ki-Back Chu
Eun-Kyung Moon
Fu-Shi Quan
Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
PLoS ONE
author_facet Swarnendu Basak
Hae-Ji Kang
Su-Hwa Lee
Ki-Back Chu
Eun-Kyung Moon
Fu-Shi Quan
author_sort Swarnendu Basak
title Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
title_short Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
title_full Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
title_fullStr Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
title_full_unstemmed Influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
title_sort influenza vaccine efficacy induced by orally administered recombinant baculoviruses.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description Although vaccine delivery through the oral route remains the most convenient and safest way for mass immunization purposes, this method is limited by the requirement for large antigen doses and low vaccine efficacy. In this study, we generated recombinant baculoviruses (rBVs) expressing influenza hemagglutinin (A/PR/8/34) and orally delivered a low dose of rBVs to evaluate its vaccine efficacy in mice. Intranasal rBV vaccination was included in the whole experiment for comparison. We found that oral vaccination elicited high levels of virus-specific IgG and IgA antibody responses in both serum and mucosal samples (lung, tracheal, intestinal, fecal and vaginal). Surprisingly, complete protection from the lethal influenza challenge was observed, as indicated by reductions in the virus titer, inflammatory cytokine production, body weight change, and enhanced survival. These results suggest that oral delivery of the influenza rBV vaccine induces mucosal and systemic immunity, which protect mice from the lethal influenza virus challenge. Oral delivery of baculovirus vaccines can be developed as an effective vaccination route.
url https://doi.org/10.1371/journal.pone.0233520
work_keys_str_mv AT swarnendubasak influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
AT haejikang influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
AT suhwalee influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
AT kibackchu influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
AT eunkyungmoon influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
AT fushiquan influenzavaccineefficacyinducedbyorallyadministeredrecombinantbaculoviruses
_version_ 1714815081423831040