Evidence map›Paper›PMID 22692757›Full record

ArticleCancer immunology, immunotherapy : CII2012

Using the allergic immune system to target cancer: activity of IgE antibodies specific for human CD20 and MUC1.

Pearline Zhaoying Teo, Paul J Utz, Joseph A Mollick

Abstract read
In one paragraph

Article 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 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. AllergoOncology in Review: Harnessing Allergy in the Field of Oncology to Improve Patient Outcomes.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Article
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  7. AllergoOncology: Role of immune cells and immune proteins.Clinical and translational allergy · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. IgE Antibodies against Cancer: Efficacy and Safety.Antibodies (Basel, Switzerland) · 2020
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  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

3 authors at 2 institutions in 1 country.

Pearline Zhaoying TeoDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA. pearline@stanfordalumni.org
Paul J Utz
Joseph A Mollick
Stanford University · USStanford Medicine · US

Funding

Strategies for Prevention of AutoimmunityU19DK061934 · NIDDK · STANFORD UNIVERSITY · PI FATHMAN, CHARLES GARRISON · 2001 to 2005
$4.4M
Using the Allergic Immune System to Target CancerK22CA111639 · NCI · STANFORD UNIVERSITY · PI MOLLICK, JOSEPH A · 2005 to 2009
$490k
Autoantigen Arrays to Select Vaccines for Model of PBCR21AR049328 · NIAMS · STANFORD UNIVERSITY · PI UTZ, PAUL JOSEPH · 2002 to 2003
$159k
NCI NIH HHS CA111639-01A1NCI NIH HHS K22 CA111639NIAID NIH HHS AI50854NIAID NIH HHS AI50865NIAMS NIH HHS AR49328NIAMS NIH HHS R21 AR049328NIDDK NIH HHS DK61934NIDDK NIH HHS U19 DK061934PHS HHS HHSN288201000034C
6 · The paper itself

Abstract

Monoclonal antibodies are widely used in the treatment of many B cell lymphomas and certain solid tumors. All currently approved therapeutic monoclonal antibodies are of the immunoglobulin G (IgG) isotype. We hypothesized that tumor-specific monoclonal antibodies of the IgE isotype may serve as effective cancer therapeutics. To test this hypothesis, we produced mouse-human chimeric IgE antibodies specific for the human B cell antigen CD20 and the epithelial antigen MUC1. We demonstrate here that anti-hCD20 IgE antibodies have in vitro cytotoxic activity when used with purified allergic effector cells derived from umbilical cord blood. At an effector-tumor ratio of 2:1, mast cells and tumor-specific IgE induced a 2.5-fold increase in tumor cell death, as compared to control IgE. Similar results were observed when eosinophils were used as effector cells. In an in vivo murine model of breast carcinoma, administration of anti-hMUC1 IgE reduced the growth of MUC1(+) tumors by 25-30 % in hFcεRI transgenic mice. In contrast, local production of IgE and cytokines chemotactic for macrophages, eosinophils and mast cells led to complete tumor eradication. These results suggest that allergic effector cells activated by IgE and cell surface antigens have the capacity to induce tumor cell death in vitro and in vivo. The use of chimeric antibodies and hFcεRI transgenic mice will greatly enhance investigations in the nascent field of allergo-oncology.

Indexed as

AnimalsAntibodies, MonoclonalAntibody SpecificityAntigens, CD20Antigens, SurfaceB-LymphocytesBreast NeoplasmsCarcinomaCell DeathCell LineCell Line, TumorChemokinesCHO CellsCricetinaeEosinophilsFemaleAntibodies, MonoclonalAntigens, CD20Antigens, SurfaceChemokinesImmunoglobulin EMUC1 protein, humanMucin-1

Identifiers

PMID22692757
PMCPMC3833261
OpenAlexW2057265591

What OpenQuestion holds

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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.