Evidence map›Paper›PMID 32203189›Full record

ArticleCellular & molecular immunology2020

Characterization of the receptor-binding domain (RBD) of 2019 novel coronavirus: implication for development of RBD protein as a viral attachment inhibitor and vaccine.

Wanbo Tai, Lei He, Xiujuan Zhang, Jing Pu, Denis Voronin, Shibo Jiang, Yusen Zhou, Lanying Du

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 971 papers.

0numbers the graph read from it
0cells of the map it votes in
971citing papers in PubMed
40.8field-weighted citation impact, top 1% 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.

NCT04530448 phase4terminatednot on this map

Coronavirus Induced Acute Kidney Injury: Prevention Using Urine Alkalinization

TypeinterventionalSponsorWest Virginia UniversityRan2020 to 2021Enrolled3ConditionsCOVID, Coronavirus, Coronavirus Infection, AKIArmsSodium bicarbonate, Standard of Care
NCT04596098 completednot on this map

Immune Responses to COVID-19 (SARS-CoV-2 Related Infection); Isolation of Human Neutralizing Monoclonal Antibodies for Therapeutics and Vaccine Design Approaches: a Prospective Monocentric Trial With Collaborative Sample Collection.

TypeobservationalSponsorUniversity Hospital, GrenobleRan2020 to 2022Enrolled55ConditionsSARS-CoV 2ArmsBlood sampling
3 · Its place in the literature

Who cites it

971 citing papers in PubMed, 1,806 citations in OpenAlex.

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  8. Machine learning-guided rational engineering of ACE2-derived peptides for broad-spectrum neutralization of SARS-CoV-2 variants.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2026
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  15. Current pharmaceutical biotechnology · 2026
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911 more citing papers are in PubMed but not listed here.

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 2 countries.

Wanbo TaiLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA.
Lei HeBeijing Institute of Microbiology and Epidemiology, Beijing, China.
Xiujuan ZhangLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA.
Jing PuLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA.
Denis VoroninLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA.ORCID http://orcid.org/0000-0003-2652-0787
Shibo JiangLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA. sjiang@nybc.org.
Yusen ZhouBeijing Institute of Microbiology and Epidemiology, Beijing, China. yszhou@bmi.ac.cn.
Lanying DuLindsley F. Kimball Research Institute, New York Blood Center, New York, NY, USA. ldu@nybc.org.
New York Blood Center · USInstitute of Microbiology · CNShanghai Medical College of Fudan University · CN

Funding

Structure-based design of coronavirus subunit vaccinesR01AI139092 · NIAID · NEW YORK BLOOD CENTER · PI DU, LANYING · 2018 to 2022
$4.2M
Rational design and evaluation of novel mRNA vaccines against MERS-CoVR01AI137472 · NIAID · NEW YORK BLOOD CENTER · PI DU, LANYING · 2018 to 2022
$4.1M
NIAID NIH HHS R01 AI137472NIAID NIH HHS R01 AI139092U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AI137472U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01AI139092
6 · The paper itself

Abstract

The outbreak of Coronavirus Disease 2019 (COVID-19) has posed a serious threat to global public health, calling for the development of safe and effective prophylactics and therapeutics against infection of its causative agent, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), also known as 2019 novel coronavirus (2019-nCoV). The CoV spike (S) protein plays the most important roles in viral attachment, fusion and entry, and serves as a target for development of antibodies, entry inhibitors and vaccines. Here, we identified the receptor-binding domain (RBD) in SARS-CoV-2 S protein and found that the RBD protein bound strongly to human and bat angiotensin-converting enzyme 2 (ACE2) receptors. SARS-CoV-2 RBD exhibited significantly higher binding affinity to ACE2 receptor than SARS-CoV RBD and could block the binding and, hence, attachment of SARS-CoV-2 RBD and SARS-CoV RBD to ACE2-expressing cells, thus inhibiting their infection to host cells. SARS-CoV RBD-specific antibodies could cross-react with SARS-CoV-2 RBD protein, and SARS-CoV RBD-induced antisera could cross-neutralize SARS-CoV-2, suggesting the potential to develop SARS-CoV RBD-based vaccines for prevention of SARS-CoV-2 and SARS-CoV infection.

Indexed as

Viral VaccinesAmino Acid SequenceAnimalsAntibodies, ViralBetacoronavirusBinding SitesChiropteraCoronavirus InfectionsCOVID-19COVID-19 VaccinesCross ReactionsHEK293 CellsHumansMicePandemicsPneumonia, ViralAntibodies, ViralCOVID-19 VaccinesReceptor, Angiotensin, Type 2Spike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Vaccines2019 novel coronaviruscross-neutralizationreceptor-binding domainSARS-CoV-2spike proteinviral inhibitor

Identifiers

PMID32203189
PMCPMC7091888
OpenAlexW3011537081

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.