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Combined anti-PD-1 and anti-CTLA-4 checkpoint blockade: Treatment of melanoma and immune mechanisms of action.
Willsmore, Zena N; Coumbe, Ben G T; Crescioli, Silvia; Reci, Sara; Gupta, Ayushi; Harris, Robert J; Chenoweth, Alicia; Chauhan, Jitesh; Bax, Heather J; McCraw, Alexa; Cheung, Anthony; Osborn, Gabriel; Hoffmann, Ricarda M; Nakamura, Mano; Laddach, Roman; Geh, Jenny L C; MacKenzie-Ross, Alastair; Healy, Ciaran; Tsoka, Sophia; Spicer, James F; Josephs, Debra H; Papa, Sophie; Lacy, Katie E; Karagiannis, Sophia N.
Affiliation
  • Willsmore ZN; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Coumbe BGT; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Crescioli S; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Reci S; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Gupta A; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Harris RJ; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Chenoweth A; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Chauhan J; Breast Cancer Now Research Unit, School of Cancer & Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, London, United Kingdom.
  • Bax HJ; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • McCraw A; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Cheung A; School of Cancer & Pharmaceutical Sciences, King's College London, London, United Kingdom.
  • Osborn G; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Hoffmann RM; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Nakamura M; Breast Cancer Now Research Unit, School of Cancer & Pharmaceutical Sciences, King's College London, Guy's Cancer Centre, London, United Kingdom.
  • Laddach R; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Geh JLC; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • MacKenzie-Ross A; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Healy C; St. John's Institute of Dermatology, School of Basic & Medical Biosciences, King's College London, London, SE1 9RT, United Kingdom.
  • Tsoka S; Department of Informatics, Faculty of Natural and Mathematical Sciences, King's College London, London, United Kingdom.
  • Spicer JF; Department of Plastic Surgery at Guy's, King's, and St. Thomas' Hospitals, London, United Kingdom.
  • Josephs DH; Department of Plastic Surgery at Guy's, King's, and St. Thomas' Hospitals, London, United Kingdom.
  • Papa S; Department of Plastic Surgery at Guy's, King's, and St. Thomas' Hospitals, London, United Kingdom.
  • Lacy KE; Department of Informatics, Faculty of Natural and Mathematical Sciences, King's College London, London, United Kingdom.
  • Karagiannis SN; School of Cancer & Pharmaceutical Sciences, King's College London, London, United Kingdom.
Eur J Immunol ; 51(3): 544-556, 2021 03.
Article in En | MEDLINE | ID: mdl-33450785
ABSTRACT
Cytotoxic T-lymphocyte associated protein-4 (CTLA-4) and the Programmed Death Receptor 1 (PD-1) are immune checkpoint molecules that are well-established targets of antibody immunotherapies for the management of malignant melanoma. The monoclonal antibodies, Ipilimumab, Pembrolizumab, and Nivolumab, designed to interfere with T cell inhibitory signals to activate immune responses against tumors, were originally approved as monotherapy. Treatment with a combination of immune checkpoint inhibitors may improve outcomes compared to monotherapy in certain patient groups and these clinical benefits may be derived from unique immune mechanisms of action. However, treatment with checkpoint inhibitor combinations also present significant clinical challenges and increased rates of immune-related adverse events. In this review, we discuss the potential mechanisms attributed to single and combined checkpoint inhibitor immunotherapies and clinical experience with their use.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / CTLA-4 Antigen / Programmed Cell Death 1 Receptor / Immune Checkpoint Inhibitors / Melanoma / Antibodies, Monoclonal Limits: Animals / Humans Language: En Journal: Eur J Immunol Year: 2021 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Neoplasms / CTLA-4 Antigen / Programmed Cell Death 1 Receptor / Immune Checkpoint Inhibitors / Melanoma / Antibodies, Monoclonal Limits: Animals / Humans Language: En Journal: Eur J Immunol Year: 2021 Document type: Article Affiliation country: United kingdom