Evidence map›Paper›PMID 20655599›Full record

ArticleVeterinary immunology and immunopathology2010

Generation and characterization of anti-alpha-enolase single-chain antibodies in chicken.

Sy-Jye Leu, Yu-Ching Lee, Neng-Yao Shih, I-Jen Huang, Ko-Jiunn Liu, Hsu-Feng Lu, Shih-Yi Huang, Yi-Yuan Yang

Abstract read
In one paragraph

Article in Veterinary immunology and immunopathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

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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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Promising immunotherapeutic targets for treating candidiasis.Frontiers in cellular and infection microbiology · 2024
    Review
  2. In Vitro Characterization of Neutralizing Hen Antibodies toInternational journal of molecular sciences · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Avian IgY antibodies and their recombinant equivalents in research, diagnostics and therapy.Biologicals : journal of the International Association of Biological Standardization · 2012
    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

8 authors at 5 institutions in 1 country.

Sy-Jye LeuDepartment of Microbiology and Immunology, School of Medicine, Taipei Medical University, Taipei 110, Taiwan.
Yu-Ching Lee
Neng-Yao Shih
I-Jen Huang
Ko-Jiunn Liu
Hsu-Feng Lu
Shih-Yi Huang
Yi-Yuan Yang
National Health Research Institutes · TWTaipei Medical University Hospital · TWCheng Hsin General Hospital · TWGenomics Research Center, Academia Sinica · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It was previously reported that up-regulation of alpha-enolase protein was detected in 65% of patients with non-small cell lung cancers (NSCLC). Moreover, a high titer of anti-alpha-enolase antibodies was developed in a smaller proportion (7.4%) of these patients than in non-tumor-associated patients and healthy subjects. In the present study, we characterized polyclonal and single-chain variable fragment (scFv) anti-alpha-enolase antibodies from immunized chickens. The E. coli-derived recombinant alpha-enolase protein was purified to its high homogenicity as verified by SDS-PAGE. After the 4th immunization, a high titer of specific polyclonal anti-alpha-enolase antibodies was elicited in immunized chickens and specifically recognized the purified human alpha-enolase antigen as determined by Western blot and ELISA. The expressed heavy and light chain variable genes (VH and VL) were isolated from spleen B cells and amplified to construct phage antibody libraries containing scFv molecules. After four rounds of panning selection, the scFv antibodies of randomly chosen clones were expressed and their binding specificity to alpha-enolase protein was verified using competitive ELISA, flow cytometry and immunofluorescence staining. Nucleotide sequence analysis from 10 alpha-enolase binding clones showed that 3 (30%) clones used identical heavy and light genes for scFv antibody expression, as represented by EnL5. Notably, amino acid changes in complementarity-determining regions (CDRs) were more frequently observed than those in framework regions (FRs) in all clones, indicating a strong affinity selection through mutations. All together, it is believed that these polyclonal and scFv IgY antibodies may be helpful in the development of molecular diagnostic and therapeutic agents for lung cancers in the future.

Indexed as

Amino Acid SequenceAnimalsChickensEnzyme-Linked Immunosorbent AssayEscherichia coliFemaleFlow CytometryFluorescent Antibody TechniqueImmunizationImmunoglobulinsMicroscopy, ConfocalMolecular Sequence DataPeptide LibraryPhosphopyruvate HydrataseRecombinant ProteinsSingle-Chain AntibodiesIgYImmunoglobulinsPeptide LibraryPhosphopyruvate HydrataseRecombinant ProteinsSingle-Chain Antibodies

Identifiers

PMID20655599
PMCPMC7112641
OpenAlexW2074493203

What OpenQuestion holds

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Registered trials

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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.