Evidence map›Paper›PMID 37006289›Full record

ArticleFrontiers in immunology2023

A humanized anti-human adenovirus 55 monoclonal antibody with good neutralization ability.

Lei Chen, Jiansheng Lu, Junjie Yue, Rong Wang, Peng Du, Yunzhou Yu, Jiazheng Guo, Xi Wang, Yujia Jiang, Kexuan Cheng and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Lei ChenAcademy of Military Medical Sciences (AMMS), Beijing, China.
Jiansheng LuAcademy of Military Medical Sciences (AMMS), Beijing, China.
Junjie YueAcademy of Military Medical Sciences (AMMS), Beijing, China.
Rong WangAcademy of Military Medical Sciences (AMMS), Beijing, China.
Peng DuAcademy of Military Medical Sciences (AMMS), Beijing, China.
Yunzhou YuAcademy of Military Medical Sciences (AMMS), Beijing, China.
Jiazheng GuoAcademy of Military Medical Sciences (AMMS), Beijing, China.
Xi WangAcademy of Military Medical Sciences (AMMS), Beijing, China.
Yujia JiangAcademy of Military Medical Sciences (AMMS), Beijing, China.
Kexuan ChengAcademy of Military Medical Sciences (AMMS), Beijing, China.
Zhixin YangAcademy of Military Medical Sciences (AMMS), Beijing, China.
Tao ZhengAcademy of Military Medical Sciences (AMMS), Beijing, China.
Academy of Military Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human adenovirus type 55 (HAdV55) has a re-emerged as pathogen causing an acute respiratory disease presenting as a severe lower respiratory illness that can cause death. To date, there is no HAdV55 vaccine or treatment available for general use. Methods: Herein, a monoclonal antibody specific for HAdV55, mAb 9-8, was isolated from an scFv-phage display library derived from mice immunized with the purified inactived-HAdV55 virions. By using ELISA and a virus micro-neutralization assay, we evaluated the binding and neutralizing activity of mAb 9-8 following humanization. Western blotting analysis and antigen-antibody molecular docking analysis were used to identify the antigenic epitopes that the humanized monoclonal antibody 9-8-h2 recognized. After that, their thermal stability was determined. Results: MAb 9-8 showed potent neutralization activity against HAdV55. After humanization, the humanized neutralizing monoclonal antibody (9-8-h2) was identified to neutralize HAdV55 infection with an IC50 of 0.6050 nM. The mAb 9-8-h2 recognized HAdV55 and HAdV7 virus particles, but not HAdV4 particles. Although mAb 9-8-h2 could recognize HAdV7, it could not neutralize HAdV7. Furthermore, mAb 9-8-h2 recognized a conformational neutralization epitope of the fiber protein and the crucial amino acid residues (Arg 288, Asp 157, and Asn 200) were identified. MAb 9-8-h2 also showed favorable general physicochemical properties, including good thermostability and pH stability. Conclusions: Overall, mAb 9-8-h2 might be a promising molecule for the prevention and treatment of HAdV55.

Indexed as

Antibodies, NeutralizingAntibodies, ViralAdenoviridaeAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedEpitopesMiceMolecular Docking SimulationAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntibodies, NeutralizingAntibodies, ViralEpitopesconformational epitopehuman adenovirus type 55(HAdV55)monoclonal antibody(mAb)neutralizing antibodyscFv-phage immune library

Identifiers

PMID37006289
PMCPMC10060833
OpenAlexW4327617437

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.