Systemic immunosuppression from ultraviolet radiation exposure inhibits cancer immunotherapy
Pedro Durao, Timothy Budden, Karthik Mallela, Martha Gutteridge, Isabella Mataloni, Shilpa Gurung, Mirco Mastrangelo, Luke Roberts, Antonia Banyard, Garry Ashton, Graham M Lord, Adam Hurlstone, Sara Valpione, Amaya Viros

TL;DR
Repeated sun exposure weakens the immune system's response to cancer immunotherapy, especially in melanoma and colorectal cancer.
Contribution
This study reveals that systemic immunosuppression from UV radiation reduces the effectiveness of immune checkpoint blockade therapy in cancer.
Findings
Chronic UVR exposure decreases immune checkpoint blockade response in mouse models of cancer.
UVR increases systemic Tregs, leading to immunosuppression in tumors and ICB resistance.
Pharmacological depletion of Tregs restores ICB response in UVR-exposed animals.
Abstract
Ultraviolet radiation (UVR) affects local cutaneous and systemic immunity acutely. The wavelength, pattern and intensity of UVR exposure, individual skin phototype and immune state of individuals modulate the impact of UVR systemically. Local cutaneous immunity after UVR leads to immunosuppression that impacts melanoma. However, the effects of systemic UVR-induced changes on solid cancer therapy are not known. We investigated the impact of repeated UVR exposure on systemic immunity and immune checkpoint blockade (ICB) tumor responses in colorectal cancer and melanoma mouse models. Animals exposed to chronic UVR exhibit decreased ICB response, which is mediated by systemic factors. Repeated UVR exposure expanded systemic lymphocyte populations and contracted total systemic myeloid cells. Specifically, UVR expanded peripheral blood CD4+ regulatory T cells (Tregs), which in turn led to…
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Taxonomy
TopicsSkin Protection and Aging · Cancer Immunotherapy and Biomarkers · Nonmelanoma Skin Cancer Studies
