Evidence map›Paper›PMID 33628623›Full record

ArticleOncoimmunology2021

IgG4 induces tolerogenic M2-like macrophages and correlates with disease progression in colon cancer.

Galateja Jordakieva, Rodolfo Bianchini, Daniel Reichhold, Jakob Piehslinger, Alina Groschopf, Sebastian A Jensen, Ettore Mearini, Giuseppe Nocentini, Richard Crevenna, Gerhard J Zlabinger and 3 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 46 citations in OpenAlex.

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  15. Advances in tumor-infiltrating B lymphocytes.Central-European journal of immunology · 2025
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  17. Tumors in the setting of dupilumab use: A review of the literature.The World Allergy Organization journal · 2025
    Review
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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

13 authors at 7 institutions in 5 countries.

Galateja JordakievaDepartment of Physical Medicine, Rehabilitation and Occupational Medicine, Vienna, Austria.ORCID 0000-0001-5884-8256
Rodolfo BianchiniThe Interuniversity Messerli Research Institute of the University of Veterinary Medicine, the Medical University of Vienna and the University of Vienna, Unit of Comparative Medicine, Vienna, Austria.ORCID 0000-0003-0351-6937
Daniel ReichholdDepartment of General Surgery, Barmherzige Schwestern Krankenhaus Wien, Vienna, Austria.
Jakob PiehslingerDepartment of General Surgery, Barmherzige Schwestern Krankenhaus Wien, Vienna, Austria.
Alina GroschopfThe Interuniversity Messerli Research Institute of the University of Veterinary Medicine, the Medical University of Vienna and the University of Vienna, Unit of Comparative Medicine, Vienna, Austria.
Sebastian A JensenDepartment of General Surgery, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-6216-193X
Ettore MeariniDepartment of Surgical and Biomedical Sciences, Urology Clinic of Perugia, University of Perugia, Perugia, Italy.ORCID 0000-0003-1652-2965
Giuseppe NocentiniSection of Pharmacology, Department of Medicine, University of Perugia, Perugia, Italy.ORCID 0000-0002-5209-0488
Richard CrevennaDepartment of Physical Medicine, Rehabilitation and Occupational Medicine, Vienna, Austria.ORCID 0000-0002-9177-0101
Gerhard J ZlabingerDivision of Clinical and Experimental Immunology, Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-7478-4173
Sophia N KaragiannisSt. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, UK.ORCID 0000-0002-4100-7810
Alexander KlausDepartment of General Surgery, Barmherzige Schwestern Krankenhaus Wien, Vienna, Austria.ORCID 0000-0003-3832-6957
Erika Jensen-JarolimThe Interuniversity Messerli Research Institute of the University of Veterinary Medicine, the Medical University of Vienna and the University of Vienna, Unit of Comparative Medicine, Vienna, Austria.ORCID 0000-0003-4019-5765
Barmherzige Schwestern Krankenhaus Wien · ATUniversity of Veterinary Medicine Vienna · ATRHI Magnesita (Austria) · ATUniversity of Perugia · ITInstitute of Immunology · HRKing's College - North Carolina · USMedical University of Vienna · AT

Funding

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

Abstract

IgG4 subclass antibodies are expressed in alternative Th2 environments featuring high IL-10 expression, including several solid tumors such as melanoma. To induce tolerance, allergen immunotherapy mediates antibody class switching from pro-inflammatory IgE to anti-inflammatory IgG4. We previously reported that IgG4 drives allergic M2 macrophages toward tolerogenic states. Here we assessed the roles of IgG4 and macrophage activation in colorectal cancer (CRC). In this observer-blinded, case-control study, we analyzed total circulating serum IgE, IgG1 and IgG4 levels in CRC (n = 38) patients with (n = 13, TxNxM1) or without (n = 25, TxNxM0) metastasis, and in healthy donors (n = 21). Primary cultures of circulating monocyte-derived macrophages from healthy controls and CRC patients were further evaluated in their responses to stimulation with IgG1 or IgG4. We found higher absolute serum levels of IgG4 in patients with CRC. IgG4 enabled polarization of macrophages derived from CRC patients and healthy controls into alternatively-activated tolerogenic M2b phenotypes. IgG4-stimulated M2 macrophages were characterized by lower surface CD206, CD163, CD14, and CD11b expression and higher CCL-1, IL-10, and IL-6 production. IgG4 was less potent that IgG1 in triggering antibody-dependent cell-mediated phagocytosis (ADCP) of cancer cells. Further, higher z-normalized IgG4/-IgE sera level ratios correlated with the presence of metastasis (

Indexed as

Colonic NeoplasmsImmunoglobulin GCase-Control StudiesDisease ProgressionHumansMacrophagesTumor MicroenvironmentImmunoglobulin GallergooncologyIgEIgG4M2btumor-associated macrophages

Identifiers

PMID33628623
PMCPMC7889146
OpenAlexW3126571838

What OpenQuestion holds

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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.