Melanomas have long been considered to be immunogenic tumors. Although anti-programmed death 1 (PD-1) therapy has been approved worldwide as first-line treatment, many patients do not benefit from it, so there is an important therapeutic gap. Adoptive cell therapy with tumor-infiltrating lymphocytes (TILs) was described in the 1980s by Rosenberg and colleagues.(1) This personalized treatment for cancer is based on the infusion of autologous T lymphocytes that have been obtained directly from surgically removed autologous tumors and then expanded in culture with the use of interleukin-2 stimulation. Both preconditioning lymphodepletion with high-dose, nonmyeloablative chemotherapy and the intravenous administration of high-dose . . .
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Dept Cardiovasc Med, Mayo Clin, 4500 San Pablo, Jacksonville, FL 32224 USA
Mayo Clin, Dept Cardiovasc Med, Jacksonville, FL USADept Cardiovasc Med, Mayo Clin, 4500 San Pablo, Jacksonville, FL 32224 USA
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Politecn Torino, Dept Appl Sci & Technol DISAT, Inst Mat Phys & Engn, POB 10129, Turin, ItalyMashhad Univ Med Sci, Sch Med, Dept Modern Sci & Technol, POB 917794-8564, Mashhad, Iran
Baino, Francesco
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Hamzehlou, Sepideh
Hill, Robert G.
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Queen Mary Univ London, Barts & London Sch Med & Dent, Unit Dent Phys Sci, Mile End Rd, London E1 4NS, EnglandMashhad Univ Med Sci, Sch Med, Dept Modern Sci & Technol, POB 917794-8564, Mashhad, Iran
Hill, Robert G.
Mozafari, Masoud
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MERC, Nanotechnol & Adv Mat Dept, Bioengn Res Grp, POB 14155-4777, Tehran, Iran
IUMS, Cellular & Mol Res Ctr, Tehran, Iran
IUMS, Fac Adv Technol Med, Dept Tissue Engn & Regenerat Med, Tehran, IranMashhad Univ Med Sci, Sch Med, Dept Modern Sci & Technol, POB 917794-8564, Mashhad, Iran