Harnessing Tumor Necrosis Factor Alpha to Achieve Effective Cancer Immunotherapy

被引:81
作者
Florencia Mercogliano, Maria [1 ]
Bruni, Sofia [2 ]
Mauro, Florencia [2 ]
Virginia Elizalde, Patricia [2 ]
Schillaci, Roxana [2 ]
机构
[1] Consejo Nacl Invest Cient & Tecn IQUIBICEN CONICE, Lab Biofisicoquim Proteinas, Inst Quim Biol, Fac Ciencias Exactas & Nat, RA-1428 Buenos Aires, DF, Argentina
[2] Inst Biol & Med Expt IBYME CONICET, Lab Mol Mech Carcinogenesis, RA-1428 Buenos Aires, DF, Argentina
关键词
TNFα immunotherapy; adoptive cell therapy; monoclonal antibody; immune checkpoint inhibitor; cancer;
D O I
10.3390/cancers13030564
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Inflammation has been acknowledged as one of the causes of increased cancer risk. Among the pro-inflammatory mediators, tumor necrosis factor alpha (TNF alpha) has been identified as an important player in cancer progression and metastasis. On the other hand, TNF alpha has a central role in promoting innate and adaptive immune responses. These apparently controversial effects are now starting to be uncovered through different studies on TNFalpha isoforms and distinct mechanisms of action of TNF alpha receptors. The use of immunotherapies for cancer treatment such as monoclonal antibodies against cancer cells or immune checkpoints and adoptive cell therapy, are beginning to broaden our understanding of TNF alpha's actions and its potential therapeutic role. This work describes TNF alpha participation as a source of treatment resistance and its implication in side effects to immunotherapy, as well as its participation in different cancer types, where TNF alpha can be a suitable target to improve therapy outcome. Tumor necrosis factor alpha (TNF alpha) is a pleiotropic cytokine known to have contradictory roles in oncoimmunology. Indeed, TNF alpha has a central role in the onset of the immune response, inducing both activation and the effector function of macrophages, dendritic cells, natural killer (NK) cells, and B and T lymphocytes. Within the tumor microenvironment, however, TNF alpha is one of the main mediators of cancer-related inflammation. It is involved in the recruitment and differentiation of immune suppressor cells, leading to evasion of tumor immune surveillance. These characteristics turn TNF alpha into an attractive target to overcome therapy resistance and tackle cancer. This review focuses on the diverse molecular mechanisms that place TNF alpha as a source of resistance to immunotherapy such as monoclonal antibodies against cancer cells or immune checkpoints and adoptive cell therapy. We also expose the benefits of TNF alpha blocking strategies in combination with immunotherapy to improve the antitumor effect and prevent or treat adverse immune-related effects.
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页码:1 / 33
页数:33
相关论文
共 350 条
[1]   SERUM LEVELS OF TUMOR-NECROSIS-FACTOR-ALPHA IN PATIENTS WITH B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA [J].
ADAMI, F ;
GUARINI, A ;
PINI, M ;
SIVIERO, F ;
SANCETTA, R ;
MASSAIA, M ;
TRENTIN, L ;
FOA, R ;
SEMENZATO, G .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (09) :1259-1263
[2]   Monoclonal antibody therapy of cancer [J].
Adams, GP ;
Weiner, LM .
NATURE BIOTECHNOLOGY, 2005, 23 (09) :1147-1157
[3]   STABILIZATION OF THE BIOACTIVITY OF TUMOR-NECROSIS-FACTOR BY ITS SOLUBLE RECEPTORS [J].
ADERKA, D ;
ENGELMANN, H ;
MAOR, Y ;
BRAKEBUSCH, C ;
WALLACH, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (02) :323-329
[4]   Suppression of Tregs by anti-glucocorticoid induced TNF receptor antibody enhances the antitumor immunity of interferon-α gene therapy for pancreatic cancer [J].
Aida, Kouichirou ;
Miyakawa, Reina ;
Suzuki, Koji ;
Narumi, Kenta ;
Udagawa, Takeshi ;
Yamamoto, Yuki ;
Chikaraishi, Tatsuya ;
Yoshida, Teruhiko ;
Aoki, Kazunori .
CANCER SCIENCE, 2014, 105 (02) :159-167
[5]   Selective inhibition of the p38 alternative activation pathway in infiltrating T cells inhibits pancreatic cancer progression [J].
Alam, Muhammad S. ;
Gaida, Matthias M. ;
Bergmann, Frank ;
Lasitschka, Felix ;
Giese, Thomas ;
Giese, Nathalia A. ;
Hackert, Thilo ;
Hinz, Ulf ;
Hussain, S. Perwez ;
Kozlov, Serguei V. ;
Ashwell, Jonathan D. .
NATURE MEDICINE, 2015, 21 (11) :1337-1343
[6]  
Antoni C, 2002, CLIN EXP RHEUMATOL, V20, pS152
[7]   Epidermal growth factor receptor transactivation mediates tumor necrosis factor-induced hepatocyte replication [J].
Argast, GM ;
Campbell, JS ;
Brooling, JT ;
Fausto, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (33) :34530-34536
[8]   Infliximab for IPILIMUMAB-Related Colitis-Letter [J].
Arriola, Edurne ;
Wheater, Matthew ;
Karydis, Ioannis ;
Thomas, Gareth ;
Ottensmeier, Christian .
CLINICAL CANCER RESEARCH, 2015, 21 (24) :5642-5643
[9]   Haematopoietic malignancies in rheumatoid arthritis:: lymphoma risk and characteristics after exposure to tumour necrosis factor antagonists [J].
Askling, J ;
Fored, CM ;
Baecklund, E ;
Brandt, L ;
Backlin, C ;
Ekbom, A ;
Sundström, C ;
Bertilsson, L ;
Cöster, L ;
Geborek, P ;
Jacobsson, LT ;
Lindblad, S ;
Lysholm, J ;
Rantapää-Dahlqvist, S ;
Saxne, T ;
Klareskog, L ;
Feltelius, N .
ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (10) :1414-1420
[10]  
Atzeni F., 2014, Autoantibodies, P795, DOI [10.1016/B978-0-444-56378-1.00092-7, DOI 10.1016/B978-0-444-56378-1.00092-7]