Evidence map›Paper›PMID 33314603›Full record

ArticleAngewandte Chemie (International ed. in English)2021

Glycoengineering of NK Cells with Glycan Ligands of CD22 and Selectins for B-Cell Lymphoma Therapy.

Senlian Hong, Chenhua Yu, Peng Wang, Yujie Shi, Weiqian Cao, Bo Cheng, Digantkumar G Chapla, Yuanhui Ma, Jie Li, Emily Rodrigues and 8 more

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 79 citations in OpenAlex.

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  18. Glycoengineering in antigen-specific immunotherapies.Current opinion in chemical biology · 2024
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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

18 authors at 5 institutions in 4 countries.

Senlian HongDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Chenhua YuDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Peng WangDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Yujie ShiDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Weiqian CaoDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Bo ChengCollege of Chemistry and Molecular Engineering, Beijing University, Beijing, 100871, China.
Digantkumar G ChaplaComplex Carbohydrate Research Center, University of Georgia, Athens, GA, 30602, USA.
Yuanhui MaDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Jie LiDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Emily RodriguesDepartment of Chemistry, University of Alberta, 11227 Saskatchewan Dr NW, Edmonton, AB, T6G 2G2, Alberta, Canada.ORCID 0000-0002-4058-7980
Yoshiki NarimatsuCopenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
John R YatesDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Xing ChenCollege of Chemistry and Molecular Engineering, Beijing University, Beijing, 100871, China.
Henrik ClausenCopenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
Kelly W MoremenComplex Carbohydrate Research Center, University of Georgia, Athens, GA, 30602, USA.
Matthew Scott MacauleyDepartment of Chemistry, University of Alberta, 11227 Saskatchewan Dr NW, Edmonton, AB, T6G 2G2, Alberta, Canada.ORCID 0000-0003-4579-1048
James C PaulsonDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Peng WuDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, 92037, USA.ORCID 0000-0002-5204-0229
Scripps Research Institute · USPeking University · CNUniversity of Alberta · CAUniversity of Copenhagen · DKUniversity of Georgia · US

Funding

Treating lung inflammation by targeting SiglecsP01HL107151 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SCHNAAR, RONALD L · 2011 to 2017
$15.4M
TR&D3. Approaches to Proteoglycan Function at Biochemical and Cellular LevelsP41GM103390 · NIGMS · UNIVERSITY OF GEORGIA · PI MOREMEN, KELLEY W. · 2012 to 2019
$14.5M
Using siglecs and their ligands to treat allergic diseases SALTADU19AI136443 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHNAAR, RONALD L · 2018 to 2022
$7.6M
Recombinant Production of Glycosylation Enzymes for Biochem/Structural StudiesP01GM107012 · NIGMS · UNIVERSITY OF GEORGIA · PI MOREMEN, KELLEY · 2013 to 2017
$7.5M
REGULATION OF SIALOSIDE EXPRESSION IN LEUKOCYTESR01AI050143 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2003 to 2018
$7.0M
Glycan dependent epitopes of HIV broadly neutralizing antibodiesR01AI113867 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C, SCHIEF, WILLIAM R. · 2014 to 2018
$4.8M
Engineer Immune Cells via Chemoenzymatic Glycan EditingR01AI143884 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI TEIJARO, JOHN ROSS, WU, PENG · 2019 to 2023
$4.7M
Origin of N-Glycan Site-Specific HeterogeneityR01GM130915 · NIGMS · UNIVERSITY OF GEORGIA · PI KANNAN, NATARAJAN, MOREMEN, KELLEY W. · 2019 to 2022
$3.4M
Chemical Tools for Studying Fucosylated GlycansR01GM093282 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI WU, PENG · 2010 to 2019
$3.4M
Exploiting inhibitory Siglecs for desensitizing mast cellsR01AI132790 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2018 to 2022
$3.1M
Chemoenzymatic methods for the detection of cellsurface glycansR01GM113046 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI WU, PENG · 2015 to 2018
$1.9M
Role of CD22 in the Germinal Center ReactionR01AI118842 · NIAID · UNIVERSITY OF ALBERTA · PI MACAULEY, MATTHEW SCOTT · 2017 to 2021
$1.4M
NHLBI NIH HHS P01 HL107151NIAID NIH HHS R01 AI050143NIAID NIH HHS R01 AI113867NIAID NIH HHS R01 AI118842NIAID NIH HHS R01 AI132790NIAID NIH HHS R01 AI143884NIAID NIH HHS U19 AI136443NIGMS NIH HHS P01 GM107012NIGMS NIH HHS P41 GM103390NIGMS NIH HHS R01 GM093282NIGMS NIH HHS R01 GM113046NIGMS NIH HHS R01 GM130915NIH HHS P01GM107012NIH HHS P01HL107151NIH HHS P41GM103390NIH HHS R01AI050143NIH HHS R01GM113046NIH HHS U19AI136443
6 · The paper itself

Abstract

CD22, a member of Siglec family of sialic acid binding proteins, has restricted expression on B cells. Antibody-based agents targeting CD22 or CD20 on B lymphoma and leukemia cells exhibit clinical efficacy for treating these malignancies, but also attack normal B cells leading to immune deficiency. Here, we report a chemoenzymatic glycocalyx editing strategy to introduce high-affinity and specific CD22 ligands onto NK-92MI and cytokine-induced natural killer cells to achieve tumor-specific CD22 targeting. These CD22-ligand modified cells exhibited significantly enhanced tumor cell binding and killing in vitro without harming healthy B cells. For effective lymphoma cell killing in vivo, we further functionalized CD22 ligand-modified NK-92MI cells with the E-selectin ligand sialyl Lewis X to promote trafficking to bone marrow. The dual-functionalized cells resulted in the efficient suppression of B lymphoma in a xenograft model. Our results suggest that natural killer cells modified with glycan ligands to CD22 and selectins promote both targeted killing of B lymphoma cells and improved trafficking to sites where the cancer cells reside, respectively.

Indexed as

Metabolic EngineeringAnimalsCarbohydrate ConformationCell Line, TumorHEK293 CellsHumansKiller Cells, NaturalLigandsLymphoma, B-CellMiceMice, Inbred NODMice, SCIDNeoplasms, ExperimentalPolysaccharidesSialic Acid Binding Ig-like Lectin 2CD22 protein, humanLigandsPolysaccharidesSialic Acid Binding Ig-like Lectin 2B-lymphomaCD22 ligandschemoenzymatic glycan editingE-selectinsLeX

Identifiers

PMID33314603
PMCPMC7980786
OpenAlexW3113017727

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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.