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Computationally Optimized SARS-CoV-2 MHC Class I and II Vaccine Formulations Predicted to Target Human Haplotype Distributions.
Liu, Ge; Carter, Brandon; Bricken, Trenton; Jain, Siddhartha; Viard, Mathias; Carrington, Mary; Gifford, David K.
  • Liu G; MIT Computer Science and Artificial Intelligence Laboratory, Cambridge, MA, USA; MIT Electrical Engineering and Computer Science, Cambridge, MA, USA.
  • Carter B; MIT Computer Science and Artificial Intelligence Laboratory, Cambridge, MA, USA; MIT Electrical Engineering and Computer Science, Cambridge, MA, USA.
  • Bricken T; Duke University, Durham, NC, USA.
  • Jain S; MIT Computer Science and Artificial Intelligence Laboratory, Cambridge, MA, USA.
  • Viard M; Basic Science Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA; Ragon Institute of Massachusetts General Hospital, MIT and Harvard University, Cambridge, MA, USA.
  • Carrington M; Basic Science Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA; Ragon Institute of Massachusetts General Hospital, MIT and Harvard University, Cambridge, MA, USA.
  • Gifford DK; MIT Computer Science and Artificial Intelligence Laboratory, Cambridge, MA, USA; MIT Electrical Engineering and Computer Science, Cambridge, MA, USA; MIT Biological Engineering, Cambridge, MA, USA. Electronic address: gifford@mit.edu.
Cell Syst ; 11(2): 131-144.e6, 2020 08 26.
Article in English | MEDLINE | ID: covidwho-676381
ABSTRACT
We present a combinatorial machine learning method to evaluate and optimize peptide vaccine formulations for SARS-CoV-2. Our approach optimizes the presentation likelihood of a diverse set of vaccine peptides conditioned on a target human-population HLA haplotype distribution and expected epitope drift. Our proposed SARS-CoV-2 MHC class I vaccine formulations provide 93.21% predicted population coverage with at least five vaccine peptide-HLA average hits per person (≥ 1 peptide 99.91%) with all vaccine peptides perfectly conserved across 4,690 geographically sampled SARS-CoV-2 genomes. Our proposed MHC class II vaccine formulations provide 97.21% predicted coverage with at least five vaccine peptide-HLA average hits per person with all peptides having an observed mutation probability of ≤ 0.001. We provide an open-source implementation of our design methods (OptiVax), vaccine evaluation tool (EvalVax), as well as the data used in our design efforts here https//github.com/gifford-lab/optivax.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Haplotypes / Viral Vaccines / Histocompatibility Antigens Class I / Histocompatibility Antigens Class II / Sequence Analysis, DNA / Vaccines, Subunit / Betacoronavirus Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Cell Syst Year: 2020 Document Type: Article Affiliation country: J.cels.2020.06.009

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Haplotypes / Viral Vaccines / Histocompatibility Antigens Class I / Histocompatibility Antigens Class II / Sequence Analysis, DNA / Vaccines, Subunit / Betacoronavirus Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Cell Syst Year: 2020 Document Type: Article Affiliation country: J.cels.2020.06.009