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NK cell receptors in anti-tumor and healthy tissue protection: Mechanisms and therapeutic advances.
Greppi, Marco; De Franco, Fabiana; Obino, Valentina; Rebaudi, Federico; Goda, Rayan; Frumento, Davide; Vita, Giorgio; Baronti, Camilla; Melaiu, Ombretta; Bozzo, Matteo; Candiani, Simona; Vellone, Valerio G; Papaccio, Federica; Pesce, Silvia; Marcenaro, Emanuela.
Afiliação
  • Greppi M; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • De Franco F; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Obino V; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Rebaudi F; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Goda R; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Frumento D; Department of Education Sciences, University of Rome Tre, Rome, Italy.
  • Vita G; Department of Internal Medicine (DIMI), University of Genoa, Genoa, Italy.
  • Baronti C; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Melaiu O; Department of Clinical Sciences and Translational Medicine, University of Rome "Tor Vergata", Rome, Italy.
  • Bozzo M; Department of Earth, Environmental and Life Sciences (DISTAV), University of Genoa, Genoa, Italy.
  • Candiani S; Department of Earth, Environmental and Life Sciences (DISTAV), University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino, Genova, Italy.
  • Vellone VG; Department of Integrated Surgical and Diagnostic Sciences (DISC), University of Genoa, Genoa, Italy; Pathology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
  • Papaccio F; Department of Medicine, Surgery and Dentistry "Scuola Medica Salernitana", University of Salerno, Baronissi, Italy. Electronic address: fpapaccio@unisa.it.
  • Pesce S; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino, Genova, Italy. Electronic address: silvia.pesce@unige.it.
  • Marcenaro E; Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy; IRCCS Ospedale Policlinico San Martino, Genova, Italy. Electronic address: emanuela.marcenaro@unige.it.
Immunol Lett ; 270: 106932, 2024 Sep 18.
Article em En | MEDLINE | ID: mdl-39303993
ABSTRACT
Natural Killer (NK) cells are integral to the innate immune system, renowned for their ability to target and eliminate cancer cells without the need for antigen presentation, sparing normal tissues. These cells are crucial in cancer immunosurveillance due to their diverse array of activating and inhibitory receptors that modulate their cytotoxic activity. However, the tumor microenvironment can suppress NK cell function through various mechanisms. Over recent decades, research has focused on overcoming these tumor escape mechanisms. Initially, efforts concentrated on enhancing T cell activity, leading to impressive results with immunotherapeutic approaches aimed at boosting T cell responses. Nevertheless, a substantial number of patients do not benefit from these treatments and continue to seek effective alternatives. In this context, NK cells present a promising avenue for developing new treatments, given their potent cytotoxic capabilities, safety profile, and activity against T cell-resistant tumors, such as those lacking HLA-I expression. Recent advancements in immunotherapy include strategies to restore and amplify NK cell activity through immune checkpoint inhibitors, cytokines, adoptive NK cell therapy, and CAR-NK cell technology. This review provides a comprehensive overview of NK cell receptors, the tumor escape mechanisms that hinder NK cell function, and the evolving field of NK cell-based cancer immunotherapy, highlighting ongoing efforts to develop more effective and targeted cancer treatment strategies.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article