2019
DOI: 10.1007/s12602-019-09598-7
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Oral Vaccination with Hepatitis E Virus Capsid Protein and Immunobiotic Bacterium-Like Particles Induce Intestinal and Systemic Immunity in Mice

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Cited by 18 publications
(14 citation statements)
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“…Furthermore, we demonstrate that our strategy not only stimulate the humoral immunity but in addition, a specific Th1 mucosal response can be also generated against the antigens administered with IBLP. Our results suggest that the adjuvant potential of IBLPs could also be exploited for subunit vaccines, as it was the case of the hepatitis E virus (HEV) capsid protein (ORF2) orally administered with IBLP1505 or IBLP027, which induced both antigen-specific humoral and cellular immune responses in mice (30). Then, the evaluation of the ability of rotavirus antigens co-administered with IBLP or fused to a LysM domain and expressed on the surface of IBLP to generate specific protective immune responses is an interesting topic of on-going research.…”
Section: Discussionmentioning
confidence: 92%
“…Furthermore, we demonstrate that our strategy not only stimulate the humoral immunity but in addition, a specific Th1 mucosal response can be also generated against the antigens administered with IBLP. Our results suggest that the adjuvant potential of IBLPs could also be exploited for subunit vaccines, as it was the case of the hepatitis E virus (HEV) capsid protein (ORF2) orally administered with IBLP1505 or IBLP027, which induced both antigen-specific humoral and cellular immune responses in mice (30). Then, the evaluation of the ability of rotavirus antigens co-administered with IBLP or fused to a LysM domain and expressed on the surface of IBLP to generate specific protective immune responses is an interesting topic of on-going research.…”
Section: Discussionmentioning
confidence: 92%
“…From that study, we were able to select a set of potential biomarkers that would allow us to efficiently select new immunobiotic strains with antiviral capabilities including IFNα, IFNβ, RIG1, TLR3, OAS1, RNASEL, MX2, A20, CXCL5, CCL4, IL-15, SELL, SELE, EPCAM, PTGS2, PLA2G4A, PTEGES, and PTGER4. Then, in order to validate this assumption, PIE cells were stimulated with different lactobacilli including immunomodulatory (L. rhamnosus CRL1505, L. plantarum CRL1506, L. rhamnosus IBL07, and L. plantarum MPL16) (8,16,24,25) and non-immunomodulatory (L. rhamnosus CRL576 and L. plantarum CRL681) strains and then challenged with poly(I:C). The expression of the biomarkers was then evaluated.…”
Section: Modulation Of Tlr3-induced Immunotranscriptome Changes In Pimentioning
confidence: 99%
“…The second is a three-dose oral vaccine consisting of proteins derived from a gt 3 strain and immunobiotic bacterium-like particles. The oral vaccine aims to induce an immune response at the site of infection and both a cellular and humoral (IgG and IgA) response have been shown in mice [95], but trials in pigs are not yet reported.…”
Section: Discussion and Hev Risk Mitigation Strategiesmentioning
confidence: 99%