Evidence map›Paper›PMID 24751715›Full record

ArticlePloS one2014

Development of VHH antibodies against dengue virus type 2 NS1 and comparison with monoclonal antibodies for use in immunological diagnosis.

Aneela Fatima, Haiying Wang, Keren Kang, Liliang Xia, Ying Wang, Wei Ye, Jufang Wang, Xiaoning Wang

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-weighted citation impact, top 9% of its field
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

29 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. An update on antiviral antibody-based biopharmaceuticals.International immunopharmacology · 2020
    Review
  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

8 authors at 3 institutions in 1 country.

Aneela FatimaSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, PR China.
Haiying WangSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, PR China.
Keren KangGuangzhou Wondfo Biotech Co., Ltd, Scientific City, Guangzhou, PR China.
Liliang XiaShanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center at Shanghai, Shanghai, PR China.
Ying WangShanghai-MOST Key Laboratory of Health and Disease Genomics, Chinese National Human Genome Center at Shanghai, Shanghai, PR China.
Wei YeSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, PR China.
Jufang WangSchool of Bioscience and Bioengineering, South China University of Technology, Guangzhou, PR China.
Xiaoning WangInstitute of Life Science, General Hospital of The People's Liberation Army, Beijing, PR China.
Bioscience (China) · CNChinese National Human Genome Center at Shanghai · CNPeople's Liberation Army No. 150 Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The possibility of using variable domain heavy-chain antibodies (VHH antibodies) as diagnostic tools for dengue virus (DENV) type 2 NS1 protein was investigated and compared with the use of conventional monoclonal antibodies. After successful expression of DENV type 2 NS1 protein, the genes of VHH antibodies against NS1 protein were biopanned from a non-immune llama library by phage display. VHH antibodies were then expressed and purified from Escherichia coli. Simultaneously, monoclonal antibodies were obtained by the conventional route. Sequence analysis of the VHH antibodies revealed novel and long complementarity determining regions 3 (CDR3). Epitope mapping was performed via a phage display peptide library using purified VHH and monoclonal antibodies as targets. Interestingly, the same region of NS1, which comprises amino acids 224HWPKPHTLW232, was conserved for both kinds of antibodies displaying the consensus motif histidine-tryptophan-tryptophan or tryptophan-proline-tryptophan. The two types of antibodies were used to prepare rapid diagnostic kits based on immunochromatographic assay. The VHH antibody immobilized rapid diagnostic kit showed better sensitivity and specificity than the monoclonal antibody immobilized rapid diagnostic kit, which might be due to the long CDR3 regions of the VHH antibodies and their ability to bind to the pocket and cleft of the targeted antigen. This demonstrates that VHH antibodies are likely to be an option for developing point-of-care tests against DENV infection.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalAntibodies, ViralChromatography, AffinityDengueDengue VirusEnzyme-Linked Immunosorbent AssayEpitope MappingFemaleImmobilized ProteinsImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionImmunologic TestsKineticsMice, Inbred BALB CAntibodies, MonoclonalAntibodies, ViralImmobilized ProteinsImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionNS1 protein, Dengue virus type 2PeptidesReagent Kits, DiagnosticRecombinant ProteinsViral Nonstructural Proteins

Identifiers

PMID24751715
PMCPMC3994031
OpenAlexW2086867356

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.