| Literature DB >> 33352267 |
Joseph S Durgin1, David M Weiner1, Maria Wysocka1, Alain H Rook2.
Abstract
Cutaneous T cell lymphomas (CTCLs) are malignancies of skin-trafficking T cells. Patients with advanced CTCL manifest immune dysfunction that predisposes to infection and suppresses the antitumor immune response. Therapies that stimulate immunity have produced superior progression-free survival compared with conventional chemotherapy, reinforcing the importance of addressing the immune deficient state in the care of patients with CTCL. Recent research has better defined the pathogenesis of these immune deficits, explaining the mechanisms of disease progression and revealing potential therapeutic targets. The features of the malignant cell in mycosis fungoides and Sézary syndrome are now significantly better understood, including the T helper 2 cell phenotype, regulatory T cell cytokine production, immune checkpoint molecule expression, chemokine receptors, and interactions with the microenvironment. The updated model of CTCL immunopathogenesis provides understanding into clinical progression and therapeutic response.Entities:
Keywords: CTCL; Sézary syndrome; cutaneous T cell lymphoma; dermatologic oncology; drug response; immune deficiency; immunopathogenesis; immunotherapy; mycosis fungoides
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Year: 2020 PMID: 33352267 PMCID: PMC7897252 DOI: 10.1016/j.jaad.2020.12.027
Source DB: PubMed Journal: J Am Acad Dermatol ISSN: 0190-9622 Impact factor: 11.527