2014
DOI: 10.4161/hv.29609
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Mucosal immunization in perspective

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Cited by 10 publications
(9 citation statements)
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“…The recent discovery of shared IgA antibody sequences in both the serum and the gut further supports the connection between steady-state circulating IgA-secreting cells and mucosa-localized cells (23). This possible shared origin, combined with the enhanced neutralization capacity of IgA antibodies, makes them an ideal target population for vaccines aimed to induce localized mucosal protection (24)(25)(26)(27)(28)(29). This current goal in vaccine development is based on the hypothesis that localized protective antibodies would prevent initial infection of the host, reducing the pathogen burden and the need for neutralizing serum IgG antibodies.…”
Section: Resultsmentioning
confidence: 85%
“…The recent discovery of shared IgA antibody sequences in both the serum and the gut further supports the connection between steady-state circulating IgA-secreting cells and mucosa-localized cells (23). This possible shared origin, combined with the enhanced neutralization capacity of IgA antibodies, makes them an ideal target population for vaccines aimed to induce localized mucosal protection (24)(25)(26)(27)(28)(29). This current goal in vaccine development is based on the hypothesis that localized protective antibodies would prevent initial infection of the host, reducing the pathogen burden and the need for neutralizing serum IgG antibodies.…”
Section: Resultsmentioning
confidence: 85%
“…Compared to systemic immunization, mucosal immunization efficiently induces a local mucosal immune response ( 102 ), which can induce “frontline immunity” with local Igs production in the MALT, neutralizing pathogens and finally preventing infection ( 103 ). Additionally, mucosal vaccines are superior to systemic vaccines from a production and regulatory standpoint ( 104 ).…”
Section: Immunoglobulin Responses Following Mucosal Immunizationmentioning
confidence: 99%
“…Sows vaccinated orally with live attenuated PEDV induced better passive protection to piglets compared to the same vaccine administered by intramuscular injection [15]. Several studies showed that mucosal immunity is induced effectively when vaccines are delivered at the mucosal surface [19], where microfold (M) cells take up and transport the antigens to dendritic cells and macrophages in the local lymph nodes to initiate antigen specific immune response. In addition, antigen specific response activated at a specific mucosal surface, such as intestine, can mediate an effector response at a distant site.…”
Section: Plos Onementioning
confidence: 99%