Evidence map›Paper›PMID 36142278›Full record

ReviewInternational journal of molecular sciences2022

Finding the Right Heavy Chains for Immunostimulatory Antibodies.

Pierre Boulard, Valérie Gouilleux-Gruart, Hervé Watier

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Targeting Co-Stimulatory Receptors of the TNF Superfamily for Cancer Immunotherapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
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

3 authors at 1 institution in 1 country.

Pierre BoulardEA7501, GICC, Faculté de Médecine, Université de Tours, F-37032 Tours, France.ORCID 0000-0002-2792-0267
Valérie Gouilleux-GruartEA7501, GICC, Faculté de Médecine, Université de Tours, F-37032 Tours, France.
Hervé WatierEA7501, GICC, Faculté de Médecine, Université de Tours, F-37032 Tours, France.ORCID 0000-0002-2139-4171
Université de Tours · FR

Funding

Agence Nationale de la Recherche ANR-10-LABX- 431 53-01
6 · The paper itself

Abstract

For twelve years, the oncology field has been revolutionized by antibodies targeting immune checkpoints. They must be considered as a heterogenous family of immunostimulatory antibodies displaying very different mechanisms of action, not only depending on the target or on the cells expressing it, but also on the IgG subclass or IgG variant that has been chosen. To dissect this complex landscape, the clinical experience has been confronted with a precise analysis of the heavy chain isotypes, referred as new Ge nomenclature. For antibodies targeting inhibitory receptors, anti-CTLA-4 antibodies (whose main effect is to kill regulatory T cells) will be distinguished from anti-PD-1 antibodies and other true antagonistic antibodies. Antibodies targeting ligands of inhibitory receptors (PD-L1, CD47) represent another different category, due to the antigen expression on tumors and a possible beneficial killing effect. The case of agonistic antibodies targeting lymphocyte activatory receptors, such as CD40 or 4-1BB, is still another "under construction" category because these products are less advanced in their clinical development. Altogether, it appears that choosing the right heavy chain is crucial to obtain the desired pharmacological effect in patients.

Indexed as

B7-H1 AntigenNeoplasmsAntibodies, MonoclonalCD47 AntigenHumansImmunoglobulin GImmunotherapyAntibodies, MonoclonalB7-H1 AntigenCD47 AntigenImmunoglobulin Gantibody engineeringFc variantsGe nomenclatureimmunoglobulin heavy chainsimmunostimulatory antibodiestherapeutic antibodies

Identifiers

PMID36142278
PMCPMC9499592
OpenAlexW4296087200

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.