Evidence map›Paper›PMID 31001248›Full record

ArticleFrontiers in immunology2019

Evaluation of

Hannah Morgan, Su-Yi Tseng, Yann Gallais, Margret Leineweber, Pascale Buchmann, Sabrina Riccardi, Myriam Nabhan, Jeannette Lo, Zaahira Gani, Natacha Szely and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

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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 7 institutions in 4 countries.

Hannah MorganTranslational Immunology, Discovery & Investigative Safety, Preclinical Safety, Novartis Institute for Biomedical Research, Basel, Switzerland.
Su-Yi TsengBiologics Research, Lead Discovery, Immunoprofiling, Bayer US LLC, San Francisco, CA, United States.
Yann GallaisInflammation, Chimiokines et Immunopathologie, INSERM, Fac. de pharmacie - Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Margret LeineweberImmunotoxicology, Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
Pascale BuchmannImmunotoxicology, Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
Sabrina RiccardiTranslational Immunology, Discovery & Investigative Safety, Preclinical Safety, Novartis Institute for Biomedical Research, Basel, Switzerland.
Myriam NabhanInflammation, Chimiokines et Immunopathologie, INSERM, Fac. de pharmacie - Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Jeannette LoBiologics Research, Lead Discovery, Immunoprofiling, Bayer US LLC, San Francisco, CA, United States.
Zaahira GaniTranslational Immunology, Discovery & Investigative Safety, Preclinical Safety, Novartis Institute for Biomedical Research, Basel, Switzerland.
Natacha SzelyInflammation, Chimiokines et Immunopathologie, INSERM, Fac. de pharmacie - Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Cornelia S ZhuImmunotoxicology, Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
Ming YangBiologics Research, Lead Discovery, Immunoprofiling, Bayer US LLC, San Francisco, CA, United States.
Andrea KiesslingTranslational Immunology, Discovery & Investigative Safety, Preclinical Safety, Novartis Institute for Biomedical Research, Basel, Switzerland.
Hans-Werner VohrImmunotoxicology, Pharmaceuticals, Research and Development, Bayer AG, Wuppertal, Germany.
Marc PallardyInflammation, Chimiokines et Immunopathologie, INSERM, Fac. de pharmacie - Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Fred AswadBiologics Research, Lead Discovery, Immunoprofiling, Bayer US LLC, San Francisco, CA, United States.
Isabelle TurbicaInflammation, Chimiokines et Immunopathologie, INSERM, Fac. de pharmacie - Univ. Paris-Sud, Université Paris-Saclay, Châtenay-Malabry, France.
Bayer (Germany) · DEBayer (United States) · USInserm · FRNovartis (Switzerland) · CHNovartis Institutes for BioMedical ResearchUniversité Paris-Saclay · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic antibodies have the potential to induce immunogenicity leading to the development of anti-drug antibodies (ADA) that consequently may result in reduced serum drug concentrations, a loss of efficacy or potential hypersensitivity reactions. Among other factors, aggregated antibodies have been suggested to promote immunogenicity, thus enhancing ADA production. Dendritic cells (DC) are the most efficient antigen-presenting cell population and are crucial for the initiation of T cell responses and the subsequent generation of an adaptive immune response. This work focuses on the development of predictive

Indexed as

Antibodies, MonoclonalBiological AssayCells, CulturedCytokinesDendritic CellsHumansAntibodies, MonoclonalCytokinesaggregatesanti-drug antibodiesdendritic cellsimmunogenicityintracellular signalingin vitro assays

Identifiers

PMID31001248
PMCPMC6455063
OpenAlexW2926267620

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.