ABSTRACT
Introduction
Near-Infrared Photoimmunotherapy (NIR-PIT) is a novel molecularly targeted phototherapy. This technique is based on a conjugate of a near-infrared photo-inducible molecule (antibody-photon absorber conjugate, APC) and a monoclonal antibody that targets a tumor-specific antigen. To date, this novel approach has been successfully applied to several types of cancer.
Areas covered
The authors discuss the possible use of NIR-PIT for the management of skin diseases, with special attention given to squamous cell carcinomas, advanced melanomas, and primary cutaneous lymphomas.
Expert opinion
NIR-PIT may be an attractive strategy for the treatment of skin disorders. The main advantage of NIR-PIT therapy is its low toxicity to healthy tissues. Cutaneous lymphocyte antigen is a potential molecular target for NIR-PIT for both cutaneous T-cell lymphomas and inflammatory skin disorders.
Article highlights
Near-Infrared Photoimmunotherapy (NIR-PIT) is based on a conjugate of a near-infrared photo-inducible molecule (antibody-photon absorber conjugate, APC) and a monoclonal antibody that targets a tumor-specific antigen.
Near-Infrared Photoimmunotherapy (NIR-PIT) has been successfully applied in several types of cancer.
Several trials have shown that Epidermal Growth Factor Receptor (EGFR)-targeted NIR-PIT is a promising therapy for recurrent and advanced head and neck squamous cell carcinomas (SCCs).
Programmed Death Ligand-1 (PD-L1)-targeted NIR-PIT may be a promising therapy for advanced melanoma.
In vitro Cutaneous Lymphocyte Antigen (CLA)-targeted NIR-PIT showed high selective cytotoxicity on a mycosis fungoides cell line.
While interfering with skin homing mechanisms seems to control Th-cell mediated skin inflammation, a skin-directed therapy based on CLA-targeted NIR-PIT may be investigated as a novel approach for the treatment of inflammatory skin disorders.
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Declaration of Interests
The authors have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
Reviewer Disclosures
Peer reviewers on this manuscript have no relevant financial relationships or otherwise to disclose.