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Delivery of MERS antigen encapsulated in α-GalCer-bearing liposomes elicits stronger antigen-specific immune responses.
Khan, Masood Alam; Malik, Ajamaluddin; Alruwetei, Abdulmohsen M; Alzohairy, Mohammad A; Alhatlani, Bader Y; Al Rugaie, Osamah; Alhumaydhi, Fahad A; Khan, Arif.
  • Khan MA; Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
  • Malik A; Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
  • Alruwetei AM; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
  • Alzohairy MA; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
  • Alhatlani BY; Department of Applied Medical Sciences, Applied College, Qassim University, Unayzah, Saudi Arabia.
  • Al Rugaie O; Department of Basic Medical Sciences, College of Medicine and Medical Sciences, Qassim University, Unayzah, Saudi Arabia.
  • Alhumaydhi FA; Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
  • Khan A; Department of Basic Health Sciences, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
J Drug Target ; 30(8): 884-893, 2022 09.
Article in English | MEDLINE | ID: covidwho-2001024
ABSTRACT
Alpha-Galactosylceramide (α-GalCer) effectively activates the natural killer T (NKT) cells to secrete remarkable amounts of Th1 and Th2 cytokines and therefore, acts as a potential immunoadjuvant in vaccine formulation. In the present study, we prepared α-GalCer-bearing or α-GalCer-free liposomes and loaded them with Middle East Respiratory Syndrome Coronavirus papain-like protease (α-GalCer-Lip-MERS-CoV PLpro or Lip-MERS-CoV PLpro). These formulations were injected in mice to investigate the antigen-specific humoral and cell-mediated immune responses. The immunisation with α-GalCer-Lip-MERS-CoV PLpro or Lip-MERS-CoV PLpro did not induce any notable toxicity in immunised mice. The results demonstrated that mice immunised with α-GalCer-Lip-MERS-CoV PLpro showed greater antigen-specific antibody titre, switching of IgG isotyping to IgG2a subclass and higher lymphocyte proliferation. Moreover, the splenocytes from α-GalCer-Lip-MERS-CoV PLpro immunised mice secreted greater levels of IFN-γ, IL-4, IL-2 and IL-12. Interestingly, a booster dose induced stronger memory immune responses in mice previously immunised with α-GalCer-Lip-MERS-CoV PLpro. In summary, α-GalCer-Lip-MERS-CoV PLpro may prove to be a promising vaccine formulation to protect the individuals against MERS-CoV infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Middle East Respiratory Syndrome Coronavirus / Liposomes Topics: Vaccines Limits: Animals Language: English Journal: J Drug Target Journal subject: Pharmacology Year: 2022 Document Type: Article Affiliation country: 1061186x.2022.2066681

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Middle East Respiratory Syndrome Coronavirus / Liposomes Topics: Vaccines Limits: Animals Language: English Journal: J Drug Target Journal subject: Pharmacology Year: 2022 Document Type: Article Affiliation country: 1061186x.2022.2066681