Evidence map›Paper›PMID 38862748›Full record

ArticleThe AAPS journal2024

Design of Crosslinking Antibodies For T-Cell Activation: Experimental and Computational Analysis of PD-1/CD137 Bispecific Agents.

Anna Kopp, Jiakun Guan, Colette Johnston, Steven Vance, James Legg, Laurie Galson-Holt, Greg M Thurber

Abstract read
In one paragraph

Article in The AAPS journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

7 authors.

Anna KoppDepartment of Chemical Engineering, University of Michigan, 2800 Plymouth Rd., Ann Arbor, Michigan, 48109, USA.
Jiakun GuanDepartment of Chemical Engineering, University of Michigan, 2800 Plymouth Rd., Ann Arbor, Michigan, 48109, USA.
Colette JohnstonCrescendo Biologics, Cambridge, UK.
Steven VanceCrescendo Biologics, Cambridge, UK.
James LeggCrescendo Biologics, Cambridge, UK.
Laurie Galson-HoltCrescendo Biologics, Cambridge, UK.
Greg M ThurberDepartment of Chemical Engineering, University of Michigan, 2800 Plymouth Rd., Ann Arbor, Michigan, 48109, USA. gthurber@umich.edu.ORCID 0000-0001-7570-2080

Funding

Maximizing Antibody Drug Conjugate Efficacy through Multiple Mechanisms of ActionR35GM128819 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Greg Thurber · 2018 to 2026
$2.8M
NIGMS NIH HHS R35 GM128819
6 · The paper itself

Abstract

Bispecific and multispecific agents have become increasingly utilized in cancer treatment and immunotherapy, yet their complex design parameters present a challenge in developing successful therapeutics. Bispecifics that crosslink receptors on two opposing cells can provide specific activation of a receptor only when these cells are in close spatial proximity, such as an immune cell and cancer cell in a tumor. These agents, including T cell activating bispecifics, can avoid off-tumor toxicity through activation only in the tumor microenvironment by utilizing a tumor target to cluster T-cell receptors for a selective costimulatory signal. Here, we investigate a panel of PD-1/CD137 targeted Humabody V

Indexed as

Antibodies, BispecificLymphocyte ActivationProgrammed Cell Death 1 ReceptorT-LymphocytesTumor Necrosis Factor Receptor Superfamily, Member 9Cross-Linking ReagentsDrug DesignHumansAntibodies, BispecificCross-Linking ReagentsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorTumor Necrosis Factor Receptor Superfamily, Member 9antibody crosslinkingbispecific antibody designcomputational modelingimmune synapse

Identifiers

PMID38862748
PMCPMC11497593

What OpenQuestion holds

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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.