P36 Investigating the role of the IgE–FcεRI axis in human cutaneous squamous cell carcinoma

Abstract Introduction and aims The IgE–FcεRI axis is primarily studied in the context of helminth infection and allergy. Here, we focus on IgE–FcεRI in skin cancer immune surveillance. We have previously shown in mouse models of cutaneous squamous cell carcinoma (cSCC) that autoreactive IgE is induced de novo and protects against cancer development via FceRI. FcεRI-expressing cells have also been reported in human solid cancers, with Fcer1a gene expression generally correlating with better disease outcomes. In mice and humans alike, mast cells and basophils express a tetrameric FcεRI (αβγ2); however, in humans FceRI is also expressed as a trimer (αγ2) on numerous myeloid cells. Knowledge of the trimeric receptor remains limited. Here, we investigate the expression-pattern of FcεRI in human cSCC and its function in tumour immunity. Methods We have used high-parameter spectral-unmixing flow cytometry and microscopy of human cSCC. To understand the in situ function of trimeric FcεRI+ cells, a humanized mouse model capable of switching to human IgE and expressing human FceRI was used. Results We report that in patients with cSCC, IgE–FcεRI+ cells decreased in blood compared with healthy controls. However, an average of 10% of tumour-infiltrating leucocytes (TILs) expressed FceRI and carried IgE, with this reaching 50% in some patients. TILs with the highest expression of FceRI included cDC2s, pDCs and a subset of CD14+MHCII+ cells; most notably, FceRI+ cDC1s and pDC increased in cSCC tissue. In humanized mice, we show that FcεRI is expressed in a human-like pattern and that administration of tumour-specific IgE reduced tumour growth in a transplantable tumour model. We are now investigating the mechanism whereby the IgE–FcεRI axis affects the tumour microenvironment and promotes antitumour immunity. Conclusions IgE–FcεRI signalling inhibits tumour growth. Understanding how this occurs will be relevant to cSCC and, more broadly, to other solid cancers, potentially unveiling novel targets for cancer immunotherapy.

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Publication Details

Journal
British Journal of Dermatology
Published
2026-01-01
DOI
https://doi.org/10.1093/bjd/ljaf429.063
Primary Topic
Mast cells and histamine
Type
article
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article

P36 Investigating the role of the IgE–FcεRI axis in human cutaneous squamous cell carcinoma

Matin Dokht Ashoori, Jessica Strid, Jennifer Shelley, Christina Malaktou et al.
British Journal of Dermatology
Mast cells and histamine
article

P36 Investigating the role of the IgE–FcεRI axis in human cutaneous squamous cell carcinoma

Matin Dokht Ashoori, Jessica Strid, Jennifer Shelley, Christina Malaktou, Holly Webster, Sophie Ward, Catherine Hardwood
article en

Abstract

Abstract Introduction and aims The IgE–FcεRI axis is primarily studied in the context of helminth infection and allergy. Here, we focus on IgE–FcεRI in skin cancer immune surveillance. We have previously shown in mouse models of cutaneous squamous cell carcinoma (cSCC) that autoreactive IgE is induced de novo and protects against cancer development via FceRI. FcεRI-expressing cells have also been reported in human solid cancers, with Fcer1a gene expression generally correlating with better disease outcomes. In mice and humans alike, mast cells and basophils express a tetrameric FcεRI (αβγ2); however, in humans FceRI is also expressed as a trimer (αγ2) on numerous myeloid cells. Knowledge of the trimeric receptor remains limited. Here, we investigate the expression-pattern of FcεRI in human cSCC and its function in tumour immunity. Methods We have used high-parameter spectral-unmixing flow cytometry and microscopy of human cSCC. To understand the in situ function of trimeric FcεRI+ cells, a humanized mouse model capable of switching to human IgE and expressing human FceRI was used. Results We report that in patients with cSCC, IgE–FcεRI+ cells decreased in blood compared with healthy controls. However, an average of 10% of tumour-infiltrating leucocytes (TILs) expressed FceRI and carried IgE, with this reaching 50% in some patients. TILs with the highest expression of FceRI included cDC2s, pDCs and a subset of CD14+MHCII+ cells; most notably, FceRI+ cDC1s and pDC increased in cSCC tissue. In humanized mice, we show that FcεRI is expressed in a human-like pattern and that administration of tumour-specific IgE reduced tumour growth in a transplantable tumour model. We are now investigating the mechanism whereby the IgE–FcεRI axis affects the tumour microenvironment and promotes antitumour immunity. Conclusions IgE–FcεRI signalling inhibits tumour growth. Understanding how this occurs will be relevant to cSCC and, more broadly, to other solid cancers, potentially unveiling novel targets for cancer immunotherapy.

British Journal of DermatologyVol. 194(1)
Queen Mary University of London (GB), Faculty of 1000 (United Kingdom) (GB), Imperial College London (GB)
Good health and well-being
Openalex Percentile: Top 95%
Mast cells and histamine
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