Evidence map›Paper›PMID 33420997›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2021

Recombinant Anti-idiotypic Antibodies in Ligand Binding Assays for Antibody Drug Development.

Stefan Harth, Christian Frisch

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

2 authors at 1 institution in 1 country.

Stefan HarthBio-Rad AbD Serotec GmbH, Puchheim, Germany.
Christian FrischBio-Rad AbD Serotec GmbH, Puchheim, Germany. christian_frisch@bio-rad.com.
Bio-Rad (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sensitive and reproducible pharmacokinetic (PK) assays and immunogenicity assessment are required as part of the complex and lengthy development process for biotherapeutic proteins. Ligand binding assays (LBAs) are included in a range of approaches applied to understand the nature and properties of the drug as well as the induction of anti-drug antibodies (ADA) against the therapeutic, which can cause adverse events and loss of efficacy. Currently, most biotherapeutics are monoclonal human or humanized antibodies. Anti-idiotypic antibodies, targeting the idiotopic determinants of individual antibody drugs are recognized as perfect reagents for such LBAs. Here we describe the typical setups for these assays and how different types of anti-biotherapeutic antibodies can be used to establish selective and sensitive assays.

Indexed as

Drug DevelopmentDrug MonitoringEpitopesImmunoassayAntibodies, Anti-IdiotypicAntibodies, Monoclonal, HumanizedAntibody SpecificityBiological ProductsHumansImmunoglobulin IdiotypesLigandsProtein BindingProteinsAntibodies, Anti-IdiotypicAntibodies, Monoclonal, HumanizedBiological ProductsEpitopesImmunoglobulin IdiotypesLigandsProteinsAnti-biotherapeutic antibodyAnti-drug antibodyAnti-idiotypic antibodyHuCALImmunogenicity assayLigand binding assayPharmacokinetic analysis

Identifiers

PMID33420997
OpenAlexW3121121438

What OpenQuestion holds

Textmetadata
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Registered trials

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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.