Evidence map›Paper›PMID 38863708›Full record

ArticleFrontiers in immunology2024

Preclinical immunogenicity risk assessment of biotherapeutics using CD4 T cell assays.

Robin E Walsh, Angela Nix, Chloé Ackaert, Aurélie Mazy, Jana Schockaert, Sofie Pattyn, Laurent Malherbe

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. 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

7 authors.

Robin E WalshLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States.
Angela NixLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States.
Chloé AckaertImmunXperts SA| Rue August Piccard 48, Gosselies, Belgium.
Aurélie MazyImmunXperts SA| Rue August Piccard 48, Gosselies, Belgium.
Jana SchockaertImmunXperts SA| Rue August Piccard 48, Gosselies, Belgium.
Sofie PattynImmunXperts SA| Rue August Piccard 48, Gosselies, Belgium.
Laurent MalherbeLilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell dependent antibody responses to biotherapeutics remain a challenge to the optimal clinical application of biotherapeutics because of their capacity to impair drug efficacy and their potential to cause safety issues. To minimize this clinical immunogenicity risk, preclinical assays measuring the capacity of biotherapeutics to elicit CD4 T cell response

Indexed as

Biological ProductsCD4-Positive T-LymphocytesDrug Evaluation, PreclinicalAntibodiesCD8-Positive T-LymphocytesCell ProliferationCells, CulturedCoculture TechniquesDendritic CellsHumansLeukocytes, MononuclearLymphocyte ActivationRisk AssessmentAntibodiesBiological ProductsCD4 T cell proliferationdendritic cellsimmunogenicitymajor histocompatibility complex class IIT cell epitopes, therapeutic proteins

Identifiers

PMID38863708
PMCPMC11165089

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.