Evidence map›Paper›PMID 26742760›Full record

ReviewCurrent allergy and asthma reports2016

IgG4 Characteristics and Functions in Cancer Immunity.

Silvia Crescioli, Isabel Correa, Panagiotis Karagiannis, Anna M Davies, Brian J Sutton, Frank O Nestle, Sophia N Karagiannis

Open access · hybridAbstract readReview
In one paragraph

Review in Current allergy and asthma reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 104 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Humoral immunity in cancer.Signal transduction and targeted therapy · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. IMGTNAR genomics and bioinformatics · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. Article

16 more citing papers are in PubMed but not listed here.

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 at 2 institutions in 3 countries.

Silvia CrescioliSt. John's Institute of Dermatology, Division of Genetics and Molecular Medicine; Faculty of Life Sciences and Medicine, King's College London, London, UK. silvia.crescioli@kcl.ac.uk.
Isabel CorreaSt. John's Institute of Dermatology, Division of Genetics and Molecular Medicine; Faculty of Life Sciences and Medicine, King's College London, London, UK. isabel.correa@kcl.ac.uk.
Panagiotis KaragiannisSt. John's Institute of Dermatology, Division of Genetics and Molecular Medicine; Faculty of Life Sciences and Medicine, King's College London, London, UK. panos.karagiannis@kcl.ac.uk.
Anna M DaviesRandall Division of Cell and Molecular Biophysics, Faculty of Life Sciences and Medicine, King's College London, London, UK. anna.davies@kcl.ac.uk.
Brian J SuttonRandall Division of Cell and Molecular Biophysics, Faculty of Life Sciences and Medicine, King's College London, London, UK. brian.sutton@kcl.ac.uk.
Frank O NestleSt. John's Institute of Dermatology, Division of Genetics and Molecular Medicine; Faculty of Life Sciences and Medicine, King's College London, London, UK. frank.nestle@kcl.ac.uk.
Sophia N KaragiannisSt. John's Institute of Dermatology, Division of Genetics and Molecular Medicine; Faculty of Life Sciences and Medicine, King's College London, London, UK. sophia.karagiannis@kcl.ac.uk.
King's College London · GBInstitute of Dermatology · TH

Funding

Cancer Research UK C30122/A11527Cancer Research UK C30122/A15774Medical Research Council G1100090Medical Research Council MR/L023091/1
6 · The paper itself

Abstract

IgG4 is the least abundant subclass of IgG in normal human serum, but elevated IgG4 levels are triggered in response to a chronic antigenic stimulus and inflammation. Since the immune system is exposed to tumor-associated antigens over a relatively long period of time, and tumors notoriously promote inflammation, it is unsurprising that IgG4 has been implicated in certain tumor types. Despite differing from other IgG subclasses by only a few amino acids, IgG4 possesses unique structural characteristics that may be responsible for its poor effector function potency and immunomodulatory properties. We describe the unique attributes of IgG4 that may be responsible for these regulatory functions, particularly in the cancer context. We discuss the inflammatory conditions in tumors that support IgG4, the emerging and proposed mechanisms by which IgG4 may contribute to tumor-associated escape from immune surveillance and implications for cancer immunotherapy.

Indexed as

Antigens, NeoplasmHumansImmunoglobulin GNeoplasmsTumor EscapeAntigens, NeoplasmImmunoglobulin GAntibodiesCancerEffector functionsIgG4Immune escapeImmunotherapy

Identifiers

PMID26742760
PMCPMC4705142
OpenAlexW2229885885

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.