Evidence map›Paper›PMID 22139135›Full record

ReviewCancer immunology, immunotherapy : CII2012

Recombinant IgE antibodies for passive immunotherapy of solid tumours: from concept towards clinical application.

Sophia N Karagiannis, Debra H Josephs, Panagiotis Karagiannis, Amy E Gilbert, Louise Saul, Sarah M Rudman, Tihomir Dodev, Alexander Koers, Philip J Blower, Christopher Corrigan and 4 more

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 2 pooled it
5.0field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 2 syntheses or guidelines pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  6. Article
  7. Review
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  9. Review
  10. Research Advances in Fusion Protein-Based Drugs for Diabetes Treatment.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  11. Review
  12. Generation and Characterization of Native and Sialic Acid-Deficient IgE.International journal of molecular sciences · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. Novel insights into the role of aptamers in the fight against cancer.Journal of cancer research and clinical oncology · 2019
    Review
  17. Review
  18. Article
  19. Review
  20. 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

14 authors at 4 institutions in 1 country.

Sophia N KaragiannisNIHR Biomedical Research Centre at Guy's and St Thomas's Hospitals and King's College London, London, UK. sophia.karagiannis@kcl.ac.uk
Debra H Josephs
Panagiotis Karagiannis
Amy E Gilbert
Louise Saul
Sarah M Rudman
Tihomir Dodev
Alexander Koers
Philip J Blower
Christopher Corrigan
Andrew J Beavil
James F Spicer
Frank O Nestle
Hannah J Gould
King's College London · GBGuy's Hospital · GBSt Thomas' Hospital · GBAsthma UK · GB

Funding

Cancer Research UK C1519/A10331Cancer Research UK C30122/A11527Medical Research Council G0400106Medical Research Council G0501494
6 · The paper itself

Abstract

Therapeutic antibodies have revolutionised treatment of some cancers and improved prognosis for many patients. Over half of those available are approved for haematological malignancies, but efficacious antibodies for solid tumours are still urgently needed. Clinically available antibodies belong to the IgG class, the most prevalent antibody class in human blood, while other classes have not been extensively considered. We hypothesised that the unique properties of IgE, a class of tissue-resident antibodies commonly associated with allergies, which can trigger powerful immune responses through strong affinity for their particular receptors on effector cells, could be employed for passive immunotherapy of solid tumours such as ovarian and breast carcinomas. Our laboratory has examined this concept by evaluating two chimaeric antibodies of the same specificity (MOv18) but different isotype, an IgG1 and an IgE against the tumour antigen folate receptor α (FRα). The latter demonstrates the potency of IgE to mount superior immune responses against tumours in disease-relevant models. We identified Fcε receptor-expressing cells, monocytes/macrophages and eosinophils, activated by MOv18 IgE to kill tumour cells by mechanisms such as ADCC and ADCP. We also applied this notion to a marketed therapeutic, the humanised IgG1 antibody trastuzumab and engineered an IgE counterpart, which retained the functions of trastuzumab in restricting proliferation of HER2/neu-expressing tumour cells but also activated effector cells to kill tumour cells by different mechanisms. On-going efficacy, safety evaluations and future first-in-man clinical studies of IgE therapeutics constitute key metrics for this concept, providing new scope for antibody immunotherapies for solid tumours.

Indexed as

AnimalsHumansImmunization, PassiveImmunoglobulin ENeoplasmsReceptors, FcImmunoglobulin EReceptors, Fc

Identifiers

PMID22139135
PMCPMC11028906
OpenAlexW2072278160

What OpenQuestion holds

Textmetadata
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.