Future perspectives on drug targeting in adult T cell leukemia-lymphoma

Abstract

Human T cell leukemia virus type 1 (HTLV-1) is the etiological agent of adult T cell leukemia/lymphoma (ATL), HTLV-1 associated myelopathy (HAM/TSP), and of a number of inflammatory diseases with an estimated 10-20 million infected individuals worldwide. Despite a number of therapeutic approaches, a cure for ATL is still in its infancy. Conventional chemotherapy has short-term efficacy, particularly in the acute subtype. Allogeneic stem cell transplantation offers long-term disease control to around one third of transplanted patients, but few can reach to transplant. This prompted, over the past recent years, the conduction of a number of clinical trials using novel treatments. Meanwhile, new data have been accumulated on biological and molecular bases of HTLV-1 transforming and infecting activity. These data offer new rational for targeted therapies of ATL. Taking into account the double-face of ATL as an hematologic malignancy as well as a viral infectious disease, this Mini-Review seeks to provide an up-to-date overview of recent efforts in the understanding of the mechanisms involved in already used therapeutic regimens showing promising results, and in selecting novel drug targets for ATL. © 2018 Marino-Merlo, Mastino, Grelli, Hermine, Bazarbachi and Macchi.

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Keywords

Antiviral agents, Atl, Biological therapy, Htlv-1, Targeted therapy, Adult, Allogeneic stem cell transplantation, Antiretroviral therapy, Article, Cell migration, Disease control, Disease exacerbation, Hematologic malignancy, Human, Human t-lymphotropic virus 1, Inflammatory disease, Molecularly targeted therapy, Protein phosphorylation, T cell leukemia, Tropical spastic paraparesis

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