tetano
Editor, Senior Moderator
ACS Appl Mater Interfaces
. 2023 Oct 30.
doi: 10.1021/acsami.3c11756. Online ahead of print. Chitosan-Alginate Polymeric Nanocomposites as a Potential Oral Vaccine Carrier Against Influenza Virus Infection
Hae-Ji Kang[SUP] 1 [/SUP], Jiaoyang Li[SUP] 2 3 [/SUP], Md Abdur Razzak[SUP] 2 3 [/SUP], Gi-Deok Eom[SUP] 1 [/SUP], Keon-Woong Yoon[SUP] 1 [/SUP], Jie Mao[SUP] 1 [/SUP], Ki-Back Chu[SUP] 1 4 [/SUP], Hui Jin[SUP] 2 [/SUP], Shin Sik Choi[SUP] 2 3 5 6 [/SUP], Fu-Shi Quan[SUP] 7 4 [/SUP]
Affiliations
Lessons from the recent COVID-19 pandemic underscore the importance of rapidly developing an efficacious vaccine and its immediate administration for prophylaxis. Oral vaccines are of particular interest, as the presence of healthcare professionals is not needed for this stress-free vaccination approach. In this study, we designed a chitosan (CH)-alginate (AL) complex carrier system encapsulating an inactivated influenza virus vaccine (A/PR/8/34, H1N1), and the efficacy of these orally administered nanocomposite vaccines was evaluated in mice. Interestingly, CH-AL complexes were able to load large doses of vaccine (≥90%) with a stable dispersion. The encapsulated vaccine was protected from gastric acid and successfully released from the nanocomposite upon exposure to conditions resembling those of the small intestines. Scanning electron microscopy of the CH-virus-AL complexes revealed that the connections between the lumps became loose and widened pores were visible on the nanocomposite's surface at pH 7.4, thereby increasing the chance of virus release into the surroundings. Orally inoculating CH-virus-AL into mice elicited higher virus-specific IgG compared to the unimmunized controls. CH-virus-AL immunization also enhanced CD4 and CD8 T cell responses while diminishing lung virus titer, inflammatory cytokine production, and body weight loss compared to the infection control group. These results suggest that chitosan-alginate polymeric nanocomposites could be promising delivery complexes for oral influenza vaccines.
Keywords: chitosan-alginate complexes; influenza virus; oral vaccine; pH responsiveness; protection.
. 2023 Oct 30.
doi: 10.1021/acsami.3c11756. Online ahead of print. Chitosan-Alginate Polymeric Nanocomposites as a Potential Oral Vaccine Carrier Against Influenza Virus Infection
Hae-Ji Kang[SUP] 1 [/SUP], Jiaoyang Li[SUP] 2 3 [/SUP], Md Abdur Razzak[SUP] 2 3 [/SUP], Gi-Deok Eom[SUP] 1 [/SUP], Keon-Woong Yoon[SUP] 1 [/SUP], Jie Mao[SUP] 1 [/SUP], Ki-Back Chu[SUP] 1 4 [/SUP], Hui Jin[SUP] 2 [/SUP], Shin Sik Choi[SUP] 2 3 5 6 [/SUP], Fu-Shi Quan[SUP] 7 4 [/SUP]
Affiliations
- PMID: 37903218
- DOI: 10.1021/acsami.3c11756
Lessons from the recent COVID-19 pandemic underscore the importance of rapidly developing an efficacious vaccine and its immediate administration for prophylaxis. Oral vaccines are of particular interest, as the presence of healthcare professionals is not needed for this stress-free vaccination approach. In this study, we designed a chitosan (CH)-alginate (AL) complex carrier system encapsulating an inactivated influenza virus vaccine (A/PR/8/34, H1N1), and the efficacy of these orally administered nanocomposite vaccines was evaluated in mice. Interestingly, CH-AL complexes were able to load large doses of vaccine (≥90%) with a stable dispersion. The encapsulated vaccine was protected from gastric acid and successfully released from the nanocomposite upon exposure to conditions resembling those of the small intestines. Scanning electron microscopy of the CH-virus-AL complexes revealed that the connections between the lumps became loose and widened pores were visible on the nanocomposite's surface at pH 7.4, thereby increasing the chance of virus release into the surroundings. Orally inoculating CH-virus-AL into mice elicited higher virus-specific IgG compared to the unimmunized controls. CH-virus-AL immunization also enhanced CD4 and CD8 T cell responses while diminishing lung virus titer, inflammatory cytokine production, and body weight loss compared to the infection control group. These results suggest that chitosan-alginate polymeric nanocomposites could be promising delivery complexes for oral influenza vaccines.
Keywords: chitosan-alginate complexes; influenza virus; oral vaccine; pH responsiveness; protection.