Evidence map›Paper›PMID 35152188›Full record

ArticleResearch in veterinary science2022

A SARS-CoV-2 nanobody that can bind to the RBD region may be used for treatment in COVID-19 in animals.

Peng Wu, Qin Yang, Xiaoli Zhao, Qingqing Liu, Jing Xi, Fan Zhang, Jinke He, Hang Yang, Chao Zhang, Zhongchen Ma and 3 more

Open access · greenAbstract read
In one paragraph

Article in Research in veterinary science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

13 authors at 1 institution in 1 country.

Peng WuCollege of Life Sciences, Shihezi University, Shihezi, China.
Qin YangCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Xiaoli ZhaoCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Qingqing LiuCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Jing XiCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Fan ZhangCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Jinke HeCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Hang YangCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Chao ZhangCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Zhongchen MaCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Xiaoyu DengCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Yong WangCollege of Animal Science and Technology, Shihezi University, Shihezi, China.
Chuangfu ChenCollege of Animal Science and Technology, Shihezi University, Shihezi, China; Key Laboratory of Prevention and Control of Animal Disease of Xinjiang Crops, Shihezi, China. Electronic address: chuangfu_chen@163.com.
Shihezi University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) caused by an infectious virus, severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2), poses a threat to the world. The suitable treatments must be identified for this disease in animals. Nanobody have therapeutic potential in the COVID-19. In this study, SARS-CoV-2 Spike RBD protein was used to make the nanobody. Nanobodies binding to the SARS-CoV-2 Spike RBD protein was obtained. Interestingly, the nanobody could bind to SARS-CoV-2 Spike S protein and RBD protein at the same time. Nanobodies were validated with a neutralizing antibody detection kit. The use of pseudoviruses confirmed that nanobodies could prevent pseudoviruses from infecting cells. We believe the nanobody are very valuable and could be used in the treatment of COVID-19. SARS-CoV-2 nanobodies can be rapidly mass-produced from microorganisms to block SARS-CoV-2 infection in vitro and in vivo with preventive and therapeutic effects.

Indexed as

COVID-19COVID-19 Drug TreatmentAnimalsAntibodies, NeutralizingAntibodies, ViralProtein BindingSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Coronavirus disease 2019NanobodyRBD proteinSARS-CoV-2S protein

Identifiers

PMID35152188
PMCPMC8821020
OpenAlexW4210936752

What OpenQuestion holds

Textmetadata
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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.