tetano
Editor, Senior Moderator
Vaccine
. 2023 Aug 22;S0264-410X(23)00969-6.
doi: 10.1016/j.vaccine.2023.08.037. Online ahead of print. Formulation development and comparability studies with an aluminum-salt adjuvanted SARS-CoV-2 spike ferritin nanoparticle vaccine antigen produced from two different cell lines
Ozan S Kumru[SUP] 1 [/SUP], Mrinmoy Sanyal[SUP] 2 [/SUP], Natalia Friedland[SUP] 2 [/SUP], John M Hickey[SUP] 1 [/SUP], Richa Joshi[SUP] 1 [/SUP], Payton Weidenbacher[SUP] 2 [/SUP], Jonathan Do[SUP] 2 [/SUP], Ya-Chen Cheng[SUP] 2 [/SUP], Peter S Kim[SUP] 3 [/SUP], Sangeeta B Joshi[SUP] 1 [/SUP], David B Volkin[SUP] 4 [/SUP]
Affiliations
The development of safe and effective second-generation COVID-19 vaccines to improve affordability and storage stability requirements remains a high priority to expand global coverage. In this report, we describe formulation development and comparability studies with a self-assembled SARS-CoV-2 spike ferritin nanoparticle vaccine antigen (called DCFHP), when produced in two different cell lines and formulated with an aluminum-salt adjuvant (Alhydrogel, AH). Varying levels of phosphate buffer altered the extent and strength of antigen-adjuvant interactions, and these formulations were evaluated for their (1) in vivo performance in mice and (2) in vitro stability profiles. Unadjuvanted DCFHP produced minimal immune responses while AH-adjuvanted formulations elicited greatly enhanced pseudovirus neutralization titers independent of ∼100%, ∼40% or ∼10% of the DCFHP antigen adsorbed to AH. These formulations differed, however, in their in vitro stability properties as determined by biophysical studies and a competitive ELISA for measuring ACE2 receptor binding of AH-bound antigen. Interestingly, after one month of 4°C storage, small increases in antigenicity with concomitant decreases in the ability to desorb the antigen from the AH were observed. Finally, we performed a comparability assessment of DCFHP antigen produced in Expi293 and CHO cells, which displayed expected differences in their N-linked oligosaccharide profiles. Despite consisting of different DCFHP glycoforms, these two preparations were highly similar in their key quality attributes including molecular size, structural integrity, conformational stability, binding to ACE2 receptor and mouse immunogenicity profiles. Taken together, these studies support future preclinical and clinical development of an AH-adjuvanted DCFHP vaccine candidate produced in CHO cells.
Keywords: Adjuvants; Alhydrogel; Comparability; Ferritin; Formulation; Nanoparticle vaccine; SARS-CoV-2 spike protein; Stability.
. 2023 Aug 22;S0264-410X(23)00969-6.
doi: 10.1016/j.vaccine.2023.08.037. Online ahead of print. Formulation development and comparability studies with an aluminum-salt adjuvanted SARS-CoV-2 spike ferritin nanoparticle vaccine antigen produced from two different cell lines
Ozan S Kumru[SUP] 1 [/SUP], Mrinmoy Sanyal[SUP] 2 [/SUP], Natalia Friedland[SUP] 2 [/SUP], John M Hickey[SUP] 1 [/SUP], Richa Joshi[SUP] 1 [/SUP], Payton Weidenbacher[SUP] 2 [/SUP], Jonathan Do[SUP] 2 [/SUP], Ya-Chen Cheng[SUP] 2 [/SUP], Peter S Kim[SUP] 3 [/SUP], Sangeeta B Joshi[SUP] 1 [/SUP], David B Volkin[SUP] 4 [/SUP]
Affiliations
- PMID: 37620203
- DOI: 10.1016/j.vaccine.2023.08.037
The development of safe and effective second-generation COVID-19 vaccines to improve affordability and storage stability requirements remains a high priority to expand global coverage. In this report, we describe formulation development and comparability studies with a self-assembled SARS-CoV-2 spike ferritin nanoparticle vaccine antigen (called DCFHP), when produced in two different cell lines and formulated with an aluminum-salt adjuvant (Alhydrogel, AH). Varying levels of phosphate buffer altered the extent and strength of antigen-adjuvant interactions, and these formulations were evaluated for their (1) in vivo performance in mice and (2) in vitro stability profiles. Unadjuvanted DCFHP produced minimal immune responses while AH-adjuvanted formulations elicited greatly enhanced pseudovirus neutralization titers independent of ∼100%, ∼40% or ∼10% of the DCFHP antigen adsorbed to AH. These formulations differed, however, in their in vitro stability properties as determined by biophysical studies and a competitive ELISA for measuring ACE2 receptor binding of AH-bound antigen. Interestingly, after one month of 4°C storage, small increases in antigenicity with concomitant decreases in the ability to desorb the antigen from the AH were observed. Finally, we performed a comparability assessment of DCFHP antigen produced in Expi293 and CHO cells, which displayed expected differences in their N-linked oligosaccharide profiles. Despite consisting of different DCFHP glycoforms, these two preparations were highly similar in their key quality attributes including molecular size, structural integrity, conformational stability, binding to ACE2 receptor and mouse immunogenicity profiles. Taken together, these studies support future preclinical and clinical development of an AH-adjuvanted DCFHP vaccine candidate produced in CHO cells.
Keywords: Adjuvants; Alhydrogel; Comparability; Ferritin; Formulation; Nanoparticle vaccine; SARS-CoV-2 spike protein; Stability.