Evidence map›Paper›PMID 38415660›Full record

ArticleMicrobiology spectrum2024

Characterization of a neutralizing antibody that recognizes a loop region adjacent to the receptor-binding interface of the SARS-CoV-2 spike receptor-binding domain.

Itsuki Anzai, Junso Fujita, Chikako Ono, Yoichiro Kosaka, Yuki Miyamoto, Shintaro Shichinohe, Kosuke Takada, Shiho Torii, Shuhei Taguwa, Koichiro Suzuki and 6 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

16 authors at 4 institutions in 1 country.

Itsuki AnzaiDepartment of Molecular Virology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.ORCID 0000-0001-9307-943X
Junso FujitaGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Chikako OnoCenter for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan.
Yoichiro KosakaBio Matrix Research Inc., Nagareyama, Chiba, Japan.
Yuki MiyamotoBio Matrix Research Inc., Nagareyama, Chiba, Japan.
Shintaro ShichinoheDepartment of Molecular Virology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Kosuke TakadaDepartment of Molecular Virology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Shiho ToriiLaboratory of Virus Control, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
Shuhei TaguwaCenter for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan.
Koichiro SuzukiThe Research Foundation for Microbial Diseases of Osaka University (BIKEN), Suita, Osaka, Japan.
Fumiaki MakinoGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Tadahiro KajitaBio Matrix Research Inc., Nagareyama, Chiba, Japan.
Tsuyoshi InoueGraduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, Japan.
Keiichi NambaGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.
Tokiko WatanabeDepartment of Molecular Virology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.ORCID 0000-0001-6461-5379
Yoshiharu MatsuuraCenter for Infectious Disease Education and Research (CiDER), Osaka University, Suita, Osaka, Japan.ORCID 0000-0001-9091-8285
The University of Osaka · JPJEOL (Japan) · JPKyoto Biken Laboratories (Japan) · JPRIKEN Center for Biosystems Dynamics Research · JP

Funding

Japan Agency for Medical Research and Development (AMED) JP19fk0108113, JP20fk0108281, JP20pc0101047Japan Agency for Medical Research and Development (AMED) JP20fk0108401, JP21fk0108493Japan Agency for Medical Research and Development (AMED) JP21am0101117, JP17pc0101020Japan Agency for Medical Research and Development (AMED) JP223fa627002Japan Agency for Medical Research and Development (AMED) JP223fa627002, JP22am0401030, JP23fk0108659, JP20jk0210021, JP22gm1610010, JP19fk0108113MEXT | Japan Science and Technology Agency (JST) JPMJMS2025MEXT | Japan Science and Technology Agency (JST) JPMJOP1861MEXT | Japan Society for the Promotion of Science (JSPS) JP20K22630MEXT | Japan Society for the Promotion of Science (JSPS) JP21H02736MEXT | Japan Society for the Promotion of Science (JSPS) JP21K15042MEXT | Japan Society for the Promotion of Science (JSPS) JP22H02521MEXT | Japan Society for the Promotion of Science (JSPS) JP25K000013Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP16H06429, JP16K21723, JP16H06432Ministry of Education, Culture, Sports, Science and Technology (MEXT) JP16H06429, JP16K21723, JP16H06434
6 · The paper itself

Abstract

Although the global crisis caused by the coronavirus disease 2019 (COVID-19) pandemic is over, the global epidemic of the disease continues. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the cause of COVID-19, initiates infection via the binding of the receptor-binding domain (RBD) of its spike protein to the human angiotensin-converting enzyme II (ACE2) receptor, and this interaction has been the primary target for the development of COVID-19 therapeutics. Here, we identified neutralizing antibodies against SARS-CoV-2 by screening mouse monoclonal antibodies and characterized an antibody, CSW1-1805, that targets a narrow region at the RBD ridge of the spike protein. CSW1-1805 neutralized several variants

Indexed as

Antibodies, NeutralizingCOVID-19Angiotensin-Converting Enzyme 2AnimalsAntibodies, ViralEpitopesHumansMiceSARS-CoV-2Spike Glycoprotein, CoronavirusAngiotensin-Converting Enzyme 2Antibodies, NeutralizingAntibodies, ViralEpitopesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2conformational transitionmonoclonal antibodyneutralizing epitopereceptor-binding domainsevere acute respiratory syndrome-coronavirus 2 (SARS-CoV-2)spike protein

Identifiers

PMID38415660
PMCPMC10986471
OpenAlexW4392232137

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.