Evidence map›Paper›PMID 37288324›Full record

ArticleOncoimmunology2023

23ME-00610, a genetically informed, first-in-class antibody targeting CD200R1 to enhance antitumor T cell function.

Jill Fenaux, Xin Fang, Yao-Ming Huang, Cristina Melero, Caroline Bonnans, Earth Light Lowe, Tiziana Palumbo, Cecilia Lay, Zuoan Yi, Aileen Zhou and 7 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

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  12. Focusing on CD8Journal of experimental & clinical cancer research : CR · 2024
    Review
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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

17 authors at 1 institution in 1 country.

Jill FenauxImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Xin FangComputational Biology, 23andMe, South San Francisco, CA, USA.
Yao-Ming HuangAntibody and Protein Engineering, 23andMe, South San Francisco, CA, USA.
Cristina MeleroAntibody and Protein Engineering, 23andMe, South San Francisco, CA, USA.
Caroline BonnansIn Vivo Pharmacology, 23andMe, South San Francisco, CA, USA.
Earth Light LoweIn Vivo Pharmacology, 23andMe, South San Francisco, CA, USA.
Tiziana PalumboIn Vivo Pharmacology, 23andMe, South San Francisco, CA, USA.
Cecilia LayImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Zuoan YiImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Aileen ZhouImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Mauro PoggioImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Wei-Jen ChungComputational Biology, 23andMe, South San Francisco, CA, USA.
Sophia R MajeedClinical Science, 23andMe, South San Francisco, CA, USA.
Dylan GlattClinical Pharmacology, 23andMe, South San Francisco, CA, USA.
Alice ChenImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
Maike SchmidtBiomarker Translation, 23andMe, South San Francisco, CA, USA.
Clarissa C LeeImmuno-Oncology, 23andMe, South San Francisco, CA, USA.
23andMe (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibition (ICI) has revolutionized cancer treatment; however, only a subset of patients benefit long term. Therefore, methods for identification of novel checkpoint targets and development of therapeutic interventions against them remain a critical challenge. Analysis of human genetics has the potential to inform more successful drug target discovery. We used genome-wide association studies of the 23andMe genetic and health survey database to identify an immuno-oncology signature in which genetic variants are associated with opposing effects on risk for cancer and immune diseases. This signature identified multiple pathway genes mapping to the immune checkpoint comprising CD200, its receptor CD200R1, and the downstream adapter protein DOK2. We confirmed that CD200R1 is elevated on tumor-infiltrating immune cells isolated from cancer patients compared to the matching peripheral blood mononuclear cells. We developed a humanized, effectorless IgG1 antibody (23ME-00610) that bound human CD200R1 with high affinity (K

Indexed as

Leukocytes, MononuclearT-LymphocytesAnimalsGenome-Wide Association StudyHumansImmunoglobulinsMiceImmunoglobulins23ME-00610cancer immunotherapyCD200CD200R1immune checkpoint

Identifiers

PMID37288324
PMCPMC10243377
OpenAlexW4379471279

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.