Evidence map›Paper›PMID 35874089›Full record

ArticleBiochemical engineering journal2022

From a recombinant key antigen to an accurate, affordable serological test: Lessons learnt from COVID-19 for future pandemics.

Renata G F Alvim, Tulio M Lima, Danielle A S Rodrigues, Federico F Marsili, Vicente B T Bozza, Luiza M Higa, Fabio L Monteiro, Daniel P B Abreu, Isabela C Leitão, Renato S Carvalho and 8 more

Abstract read
In one paragraph

Article in Biochemical engineering journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Dynamics of SARS-CoV-2 seroassay sensitivity: a systematic review and modelling study.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2023
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Ultrafast and high-throughput immunoassay assay to detect anti-SARS-CoV-2 IgG antibodies in dogs and cats.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

18 authors.

Renata G F AlvimCOPPE, Chemical Engineering Program, Cell Culture Engineering Lab, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Tulio M LimaCOPPE, Chemical Engineering Program, Cell Culture Engineering Lab, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Danielle A S RodriguesInstitute of Biophysics Carlos Chagas Filho, Program in Immunobiology, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Federico F MarsiliCOPPE, Chemical Engineering Program, Cell Culture Engineering Lab, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Vicente B T BozzaInstitute of Biophysics Carlos Chagas Filho, Program in Immunobiology, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Luiza M HigaBiology Institute, Genetics Dept., Molecular Virology Lab., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Fabio L MonteiroBiology Institute, Genetics Dept., Molecular Virology Lab., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Daniel P B AbreuCOPPE, Chemical Engineering Program, Cell Culture Engineering Lab, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Isabela C LeitãoInstitute of Biophysics Carlos Chagas Filho, Program in Immunobiology, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Renato S CarvalhoSchool of Pharmacy, Pharmaceutical Biotechnology Dept., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Rafael M GalliezMedical School, Infectious and Parasitic Disease Dept., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Terezinha M P P CastineirasMedical School, Infectious and Parasitic Disease Dept., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Leonardo H TravassosInstitute of Biophysics Carlos Chagas Filho, Program in Immunobiology, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Alberto NobregaInstitute of Microbiology, Immunology Dept., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Amilcar TanuriBiology Institute, Genetics Dept., Molecular Virology Lab., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Orlando C FerreiraBiology Institute, Genetics Dept., Molecular Virology Lab., Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
André M ValeInstitute of Biophysics Carlos Chagas Filho, Program in Immunobiology, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.
Leda R CastilhoCOPPE, Chemical Engineering Program, Cell Culture Engineering Lab, Universidade Federal do Rio de Janeiro - UFRJ, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serological tests detect antibodies generated by infection or vaccination, and are indispensable tools along different phases of a pandemic, from early monitoring of pathogen spread up to seroepidemiological studies supporting immunization policies. This work discusses the development of an accurate and affordable COVID-19 antibody test, from production of a recombinant protein antigen up to test validation and economic analysis. We first developed a cost-effective, scalable technology to produce SARS-COV-2 spike protein and then used this antigen to develop an enzyme-linked immunosorbent assay (ELISA). A receiver operator characteristic (ROC) analysis allowed optimizing the cut-off and confirmed the high accuracy of the test: 98.6% specificity and 95% sensitivity for 11+ days after symptoms onset. We further showed that dried blood spots collected by finger pricking on simple test strips could replace conventional plasma/serum samples. A cost estimate was performed and revealed a final retail price in the range of one US dollar, reflecting the low cost of the ELISA test platform and the elimination of the need for venous blood sampling and refrigerated sample handling in clinical laboratories. The presented workflow can be completed in 4 months from first antigen expression to final test validation. It can be applied to other pathogens and in future pandemics, facilitating reliable and affordable seroepidemiological surveillance also in remote areas and in low-income countries.

Indexed as

COVID-19Detection of antibodies elicited by infection or vaccinationDried blood spot for diagnostic testingPurification of SARS-COV-2 spike proteinRecombinant antigen production in mammalian cellsSerological test development

Identifiers

PMID35874089
PMCPMC9287463

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.