2020
DOI: 10.1016/j.ijbiomac.2020.02.287
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Alginate-coated chitosan nanoparticles act as effective adjuvant for hepatitis A vaccine in mice

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Cited by 52 publications
(31 citation statements)
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“…In recent years, several studies involving nanoparticles have reported satisfactory results for the control of HBV-A and HBV-B A potential vaccine based in alginate-coated chitosan nanoparticles (ACNp) loaded with hepatitis B surface antibodies (HBsAg) and anchored with lipopolysaccharide, as adjuvant for oral mucosal immunization, showed that HBsAg was protected by the nanoparticles, and it was detected that a significant production of immunoglobulin A (sIgA) in mucosal, and IgG antibodies in blood circulation. [102] Similar results were reported by AbdelAllah et al, [103] where ACNp was evaluated as effective adjuvant for hepatitis A. Nanoparticle application in mice showed production of interferon gamma (INF-γ), interleukin-10 (IL-10), and an increase in seroconversion rate (100%), splenocyte proliferation, and hepatitis A antibodies level. Given that HBV can cause hepatocellular injury, polypeptide penetratin-based hybrid nanoparticle system carrying IL-22 gene demonstrated that locally IL-22 protein (interleukin-22) expression and activation of STAT3 signaling pathway allowed to repair hepatocyte injury.…”
Section: Nanoparticles For Hepatitis Virus Infectionsupporting
confidence: 74%
“…In recent years, several studies involving nanoparticles have reported satisfactory results for the control of HBV-A and HBV-B A potential vaccine based in alginate-coated chitosan nanoparticles (ACNp) loaded with hepatitis B surface antibodies (HBsAg) and anchored with lipopolysaccharide, as adjuvant for oral mucosal immunization, showed that HBsAg was protected by the nanoparticles, and it was detected that a significant production of immunoglobulin A (sIgA) in mucosal, and IgG antibodies in blood circulation. [102] Similar results were reported by AbdelAllah et al, [103] where ACNp was evaluated as effective adjuvant for hepatitis A. Nanoparticle application in mice showed production of interferon gamma (INF-γ), interleukin-10 (IL-10), and an increase in seroconversion rate (100%), splenocyte proliferation, and hepatitis A antibodies level. Given that HBV can cause hepatocellular injury, polypeptide penetratin-based hybrid nanoparticle system carrying IL-22 gene demonstrated that locally IL-22 protein (interleukin-22) expression and activation of STAT3 signaling pathway allowed to repair hepatocyte injury.…”
Section: Nanoparticles For Hepatitis Virus Infectionsupporting
confidence: 74%
“…The numerous recent hepatitis A outbreaks emphasize the need for vaccination; despite the effectiveness of the current vaccination, further development is needed to overcome its high cost plus some immune response limitations. AbdelaAllah et al [212] evaluated the use of CS and ALG-coated CS NPs as an adjuvant/carrier for the hepatitis A (HA) vaccine against the traditional adjuvant alum (AL). Immune responses towards the HA-AL, HA-CS, and HA-ALG/CS NPs were assessed in mice.…”
Section: Vaccine Deliverymentioning
confidence: 99%
“…In a recent study, an effective adjuvant for Hepatitis A vaccine was used and compared with traditional alum adjuvant [ 34 ]. The immune response of vaccines was evaluated.…”
Section: The Role Of Alginate-based Adjuvant and Vaccine Delivery System For Pandemic Strainsmentioning
confidence: 99%