Evidence map›Paper›PMID 21559411›Full record

ArticlePloS one2011

Monitoring the systemic human memory B cell compartment of melanoma patients for anti-tumor IgG antibodies.

Amy E Gilbert, Panagiotis Karagiannis, Tihomir Dodev, Alexander Koers, Katie Lacy, Debra H Josephs, Pooja Takhar, Jenny L C Geh, Ciaran Healy, Mark Harries and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

61 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Poor Outcome in Postpartum Breast Cancer Patients Is Associated with Distinct Molecular and Immunologic Features.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  18. Article
  19. Review
  20. Multicellular network analysis of melanoma heterogeneity by scRNA-seq.American journal of translational research · 2023
    Article

1 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

19 authors at 7 institutions in 2 countries.

Amy E GilbertCutaneous Medicine and Immunotherapy Unit, Division of Genetics and Molecular Medicine, NIHR Biomedical Research Centre at Guy's and St. Thomas's Hospitals and King's College London, King's College London School of Medicine, St. John's Institute of Dermatology, Guy's Hospital, King's College London, London, United Kingdom.
Panagiotis Karagiannis
Tihomir Dodev
Alexander Koers
Katie Lacy
Debra H Josephs
Pooja Takhar
Jenny L C Geh
Ciaran Healy
Mark Harries
Katharine M Acland
Sarah M Rudman
Rebecca L Beavil
Philip J Blower
Andrew J Beavil
Hannah J Gould
James Spicer
Frank O Nestle
Sophia N Karagiannis
King's College London · GBGuy's Hospital · GBGuy's and St Thomas' NHS Foundation Trust · GBAsthma UK · GBKing's College Hospital · GBLondon Cancer · GBSt. Thomas Hospital · CA

Funding

Cancer Research UK C1519/A10331Cancer Research UK C30122/A11527Department of HealthMedical Research Council G0501494Medical Research Council G1000758
6 · The paper itself

Abstract

Melanoma, a potentially lethal skin cancer, is widely thought to be immunogenic in nature. While there has been much focus on T cell-mediated immune responses, limited knowledge exists on the role of mature B cells. We describe an approach, including a cell-based ELISA, to evaluate mature IgG antibody responses to melanoma from human peripheral blood B cells. We observed a significant increase in antibody responses from melanoma patients (n = 10) to primary and metastatic melanoma cells compared to healthy volunteers (n = 10) (P<0.0001). Interestingly, we detected a significant reduction in antibody responses to melanoma with advancing disease stage in our patient cohort (n = 21) (P<0.0001). Overall, 28% of melanoma patient-derived B cell cultures (n = 1,800) compared to 2% of cultures from healthy controls (n = 600) produced antibodies that recognized melanoma cells. Lastly, a patient-derived melanoma-specific monoclonal antibody was selected for further study. This antibody effectively killed melanoma cells in vitro via antibody-mediated cellular cytotoxicity. These data demonstrate the presence of a mature systemic B cell response in melanoma patients, which is reduced with disease progression, adding to previous reports of tumor-reactive antibodies in patient sera, and suggesting the merit of future work to elucidate the clinical relevance of activating humoral immune responses to cancer.

Indexed as

Antibodies, MonoclonalAntibodies, NeoplasmB-LymphocytesCase-Control StudiesCell LineCell Line, TumorCohort StudiesDisease ProgressionEnzyme-Linked Immunosorbent AssayFibroblastsHumansImmune SystemImmunoglobulin GImmunohistochemistryMelanomaTime FactorsAntibodies, MonoclonalAntibodies, NeoplasmImmunoglobulin G

Identifiers

PMID21559411
PMCPMC3084832
OpenAlexW2148830146

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.