Evidence map›Paper›PMID 31867291›Full record

ArticleFrontiers in cellular and infection microbiology2019

A Murine Monoclonal Antibody With Potent Neutralization Ability Against Human Adenovirus 7.

Rong Wang, Jiansheng Lu, Quan Zhou, Lei Chen, Ying Huang, Yunzhou Yu, Zhixin Yang

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

7 authors.

Rong WangLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Jiansheng LuLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Quan ZhouLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Lei ChenLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Ying HuangLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Yunzhou YuLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
Zhixin YangLaboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B1-type human adenoviruses (HAdVs) HAdV-3, HAdV-7, and HAdV-55 have caused epidemics in North America, Asia, and Europe. However, to date, no adenovirus vaccines or antiviral drugs have been approved for general use. In the present work, a scFv-phage immune library was constructed and mouse monoclonal antibody (MMAb) 10G12 was obtained through selection. 10G12 is specific for HAdV-7 and binds the hexon loop1 and loop2 (LP12), resulting in strong neutralization activity against HAdV-7. Additionally, it is stable in serum and buffer at various pH values. The findings provide insight into adenovirus and antibody responses and may facilitate the design and development of adenovirus vaccines and antiviral drugs.

Indexed as

Adenoviruses, HumanAdenovirus Infections, HumanAnimalsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralCell Line, TumorCell Surface Display TechniquesEnzyme-Linked Immunosorbent AssayEpitope MappingFemaleHost-Pathogen InteractionsHumansHydrogen-Ion ConcentrationMiceNeutralization TestsAntibodies, MonoclonalAntibodies, NeutralizingAntibodies, ViralSingle-Chain Antibodiesantiviral drugshuman adenovirus type 7 (HAdV-7)immune librarymouse monoclonal antibody (MMAb)neutralizing antibody

Identifiers

PMID31867291
PMCPMC6904267

What OpenQuestion holds

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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.