Evidence map›Paper›PMID 34654739›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

A class II MHC-targeted vaccine elicits immunity against SARS-CoV-2 and its variants.

Novalia Pishesha, Thibault J Harmand, Paul W Rothlauf, Patrique Praest, Ryan K Alexander, Renate van den Doel, Mariel J Liebeskind, Maria A Vakaki, Nicholas McCaul, Charlotte Wijne and 11 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Sortase A Catalyzed Transpeptidation for Protein Bioengineering.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
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  12. Review
  13. An antibody from single human VScience immunology · 2022
    Article
  14. Article
  15. Aptamers as promising nanotheranostic tools in the COVID-19 pandemic era.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2022
    Review
  16. Enzymatic C-to-C Protein Ligation.Angewandte Chemie (International ed. in English) · 2022
    Article
  17. T cells in SARS-CoV-2 infection and vaccination.Therapeutic advances in vaccines and immunotherapy · 2022
    Review
  18. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Novalia PisheshaSociety of Fellows, Harvard University, Cambridge, MA 02138; novalia.pishesha@childrens.harvard.edu hidde.ploegh@childrens.harvard.edu.
Thibault J HarmandProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Paul W RothlaufDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-0941-4467
Patrique PraestDepartment of Medical Microbiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
Ryan K AlexanderProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Renate van den DoelProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Mariel J LiebeskindDepartment of Genetics, Washington University School of Medicine, St. Louis, MO 63110.
Maria A VakakiDepartment of Genetics, Washington University School of Medicine, St. Louis, MO 63110.
Nicholas McCaulProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Charlotte WijneProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Elisha VerhaarProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
William PinneyProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Hailey HestonProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115.
Louis-Marie BloyetDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-5648-3190
Marjorie Cornejo PontelliDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110.
Ma Xenia G IlaganHigh Throughput Screening Center, Washington University School of Medicine, St. Louis, MO 63110.
Robert Jan LebbinkDepartment of Medical Microbiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
William J BuchserDepartment of Genetics, Washington University School of Medicine, St. Louis, MO 63110.
Emmanuel J H J WiertzDepartment of Medical Microbiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.ORCID 0000-0001-6080-7058
Sean P J WhelanDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0003-1564-8590
Hidde L PloeghProgram in Cellular and Molecular Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115; novalia.pishesha@childrens.harvard.edu hidde.ploegh@childrens.harvard.edu.ORCID 0000-0002-1090-6071

Funding

Imposing order on the family of ubiquitin-conjugating (E2) enzymes through intracellular perturbation with nanobodiesDP1AI150593 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI PLOEGH, HIDDE L. · 2019 to 2023
$7.1M
NIAID NIH HHS DP1 AI150593NIH HHS 1DP1 AI150593-01
6 · The paper itself

Abstract

The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in over 100 million infections and millions of deaths. Effective vaccines remain the best hope of curtailing SARS-CoV-2 transmission, morbidity, and mortality. The vaccines in current use require cold storage and sophisticated manufacturing capacity, which complicates their distribution, especially in less developed countries. We report the development of a candidate SARS-CoV-2 vaccine that is purely protein based and directly targets antigen-presenting cells. It consists of the SARS-CoV-2 Spike receptor-binding domain (Spike

Indexed as

PandemicsAmino Acid SequenceAnimalsAntibodies, NeutralizingAntibodies, ViralAntigen-Presenting CellsCamelids, New WorldCD8-Positive T-LymphocytesCOVID-19COVID-19 VaccinesFemaleHistocompatibility Antigens Class IIHumansImmunity, CellularImmunity, HumoralImmunization, SecondaryAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesHistocompatibility Antigens Class IIRecombinant Fusion ProteinsSingle-Domain AntibodiesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19nanobodyvaccine

Identifiers

PMID34654739
PMCPMC8612213

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.