Evidence map›Paper›PMID 40775487›Full record

ArticleNature reviews. Immunology2025

Fifty years of monoclonals: the past, present and future of antibody therapeutics.

Andrew C Chan, Greg D Martyn, Paul J Carter

Erratum issuedAbstract readHistorical Article
PubMed Publisher
In one paragraph

Article in Nature reviews. Immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Andrew C ChanDepartment of Research Biology, Genentech, South San Francisco, CA, USA. acc@gene.com.ORCID http://orcid.org/0000-0001-7523-6139
Greg D MartynDepartment of Antibody Engineering, Genentech, South San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-7373-7834
Paul J CarterDepartment of Antibody Engineering, Genentech, South San Francisco, CA, USA. pjc@gene.com.ORCID http://orcid.org/0000-0001-7854-062X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 1975, Köhler and Milstein invented hybridoma technology for the generation of murine monoclonal antibodies with predetermined antigen-binding specificity. The transformative impact of monoclonal antibodies is demonstrated by their ubiquitous use as biomedical research reagents and the worldwide approval of at least 212 antibody therapeutics with tens of millions of patients treated to date. Advances in antibody technologies, such as humanization and robust methods for human antibody generation, mitigated the major limitations of murine antibodies as therapeutics. These technologies, combined with progress in biomanufacturing, helped to launch this modern era of antibody therapeutics. Beyond IgG, antibody therapeutics have blossomed into multiple alternative formats, including bispecific antibodies and antibody-drug conjugates. Additionally, antibody fragments have been developed as stand-alone therapeutics and to target cell therapies, notably chimeric antigen receptor T cells. These advances in antibody technologies, plus innovation enabling subcutaneous delivery, have improved the therapeutic benefits and convenience of antibody treatment for many patients. This concept is illustrated here by multiple generations of antibody therapeutics for human epidermal growth factor receptor 2 (HER2)

Indexed as

Antibodies, MonoclonalImmunotherapyNeoplasmsAnimalsAntibodies, BispecificErb-b2 Receptor Tyrosine KinasesHistory, 20th CenturyHistory, 21st CenturyHumansAntibodies, BispecificAntibodies, MonoclonalERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

What OpenQuestion holds

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Read underepoch 390

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.