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http://hdl.handle.net/11452/25848
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DC Field | Value | Language |
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dc.contributor.author | Pedrazzoli, Paolo | - |
dc.contributor.author | Comoli, Patrizia | - |
dc.contributor.author | Montagna, Daniela | - |
dc.contributor.author | Bregni, Marco | - |
dc.date.accessioned | 2022-04-19T06:49:02Z | - |
dc.date.available | 2022-04-19T06:49:02Z | - |
dc.date.issued | 2012-08 | - |
dc.identifier.citation | Pedrazzoli, P. vd. (2012). "Is adoptive T-cell therapy for solid tumors coming of age". Bone Marrow Transplantation, 47(8), 1013-1019. | en_US |
dc.identifier.issn | 0268-3369 | - |
dc.identifier.issn | 1476-5365 | - |
dc.identifier.uri | https://doi.org/10.1038/bmt.2011.155 | - |
dc.identifier.uri | https://www.nature.com/articles/bmt2011155 | - |
dc.identifier.uri | http://hdl.handle.net/11452/25848 | - |
dc.description.abstract | Among the novel biological therapeutics that will increase our ability to cure human cancer in years to come, adoptive cellular therapy is one of the most promising approaches. Although this is a complex and challenging field, there have been major advances in basic and translational research resulting in clinical trial activity that is now beginning to confirm this promise. The results obtained with tumor-infiltrating lymphocytes therapy for melanoma, and virus-specific CTLs for EBV-associated malignancies are encouraging in terms of both ability to obtain clinical benefit and limited toxicity profile. In both settings, objective responses were obtained in at least 50% of treated patients. However, improvements to the clinical protocols, in terms of better patient selection and timing of administration, as well as cell product quality and availability, are clearly necessary to further ameliorate outcome, and logistical solutions are warranted to extend T-cell therapy beyond academic centers. In particular, there is a need to simplify cell production, in order to decrease costs and ease preparation. Promising implementations are underway, including harnessing the therapeutic potential of T cells transduced with TCRs directed against shared tumor antigens, and delineating strategies aimed at targeting immune evasion mechanisms exerted by tumor cells. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springernature | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Biophysics | en_US |
dc.subject | Oncology | en_US |
dc.subject | Hematology | en_US |
dc.subject | Immunology | en_US |
dc.subject | Transplantation | en_US |
dc.subject | Immunotherapy | en_US |
dc.subject | Solid tumors | en_US |
dc.subject | T-cells | en_US |
dc.subject | Epstein-barr-virus | en_US |
dc.subject | Activated killer-cells | en_US |
dc.subject | Lymphoproliferative disease | en_US |
dc.subject | Metastatic melanoma | en_US |
dc.subject | Nasopharyngeal carcinoma | en_US |
dc.subject | Successful | en_US |
dc.subject | Antitumor-activity | en_US |
dc.subject | Phase-i | en_US |
dc.subject | Lymphocytes | en_US |
dc.subject | Expansion | en_US |
dc.subject.mesh | Adoptive transfer | en_US |
dc.subject.mesh | Epstein-barr virus infections | en_US |
dc.subject.mesh | Herpesvirus 4, human | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunity, cellular | en_US |
dc.subject.mesh | Melanoma | en_US |
dc.subject.mesh | Receptors, antigen, t-cell | en_US |
dc.subject.mesh | T-lymphocytes | en_US |
dc.subject.mesh | Transduction, genetic | en_US |
dc.subject.mesh | Tumor escape | en_US |
dc.title | Is adoptive T-cell therapy for solid tumors coming of age | en_US |
dc.type | Review | en_US |
dc.identifier.wos | 000307648300001 | tr_TR |
dc.identifier.scopus | 2-s2.0-84864866991 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı. | tr_TR |
dc.identifier.startpage | 1013 | tr_TR |
dc.identifier.endpage | 1019 | tr_TR |
dc.identifier.volume | 47 | tr_TR |
dc.identifier.issue | 8 | tr_TR |
dc.relation.journal | Bone Marrow Transplantation | tr_TR |
dc.contributor.buuauthor | Demirer, Taner | - |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 21804611 | tr_TR |
dc.subject.wos | Biophysics | en_US |
dc.subject.wos | Oncology | en_US |
dc.subject.wos | Hematology | en_US |
dc.subject.wos | Immunology | en_US |
dc.subject.wos | Transplantation | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 55393694800 | tr_TR |
dc.subject.scopus | Cytokine Induced Killer Cell; Chimeric Antigen Receptor Immunotherapy; Immunotherapy | en_US |
dc.subject.emtree | Chimeric protein | en_US |
dc.subject.emtree | Tumor antigen | en_US |
dc.subject.emtree | Virus antigen | en_US |
dc.subject.emtree | Adoptive t cell therapy | en_US |
dc.subject.emtree | Allogeneic hematopoietic stem cell transplantation | en_US |
dc.subject.emtree | Cancer control | en_US |
dc.subject.emtree | Cell specificity | en_US |
dc.subject.emtree | Cell therapy | en_US |
dc.subject.emtree | Cell transfer | en_US |
dc.subject.emtree | Clinical effectiveness | en_US |
dc.subject.emtree | Cytokine induced killer cell | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Immunosurveillance | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Protein expression | en_US |
dc.subject.emtree | Review | en_US |
dc.subject.emtree | Solid tumor | en_US |
dc.subject.emtree | T lymphocyte | en_US |
dc.subject.emtree | Tumor associated leukocyte | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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