Evidence map›Paper›PMID 33953162›Full record

ArticleNature communications2021

Selection of a picomolar antibody that targets CXCR2-mediated neutrophil activation and alleviates EAE symptoms.

Xiaojie Shi, Yue Wan, Nan Wang, Jiangchao Xiang, Tao Wang, Xiaofeng Yang, Ju Wang, Xuxue Dong, Liang Dong, Lei Yan and 8 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Interleukin-8 in health and disease.Molecular biomedicine · 2026
    Review
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  12. Article
  13. Knockdown ofFrontiers in pharmacology · 2024
    Article
  14. Article
  15. Article
  16. 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

18 authors at 3 institutions in 2 countries.

Xiaojie Shi *Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Yue Wan *Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Nan Wang *Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Jiangchao Xiang *Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Tao WangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Xiaofeng YangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Ju WangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Xuxue DongShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Liang DongShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Lei YanShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Yu LiShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Lili LiuShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Shinchen HouShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Zhenwei ZhongShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.
Ian A WilsonDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, California, CA, USA.ORCID 0000-0002-6469-2419
Bei YangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China.ORCID 0000-0001-5389-3859
Guang YangShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China. yangguang@shanghaitech.edu.cn.
Richard A LernerShanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, Shanghai, China. rlerner@scripps.edu.
ShanghaiTech University · CNChinese Academy of Sciences · CNScripps Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Receptors and their ligands are important therapeutic targets for about one third of marketed drugs. Here, we describe an epitope-guided approach for selection of antibodies that modulate cellular signaling of targeted receptors. We chose CXC chemokine receptor 2 (CXCR2) in the G-protein coupled receptor superfamily as receptor and a CXCR2 N-terminal peptide for antibody selection. We obtain a highly selective, tight-binding antibody from a 10

Indexed as

AnimalsAntibodiesBinding SitesChemokinesChemotaxisEncephalomyelitis, Autoimmune, ExperimentalEndocytosisEpitopesHumansImmunoglobulin GInterleukin-8LigandsMiceNeutrophil ActivationReceptors, Interleukin-8BSignal TransductionAntibodiesChemokinesEpitopesImmunoglobulin GInterleukin-8LigandsReceptors, Interleukin-8BTumor Necrosis Factor-alpha

Identifiers

PMID33953162
PMCPMC8100106
OpenAlexW3159013796

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.