دورية أكاديمية

Chimeric antigen receptor-engineered T cells for cancer immunotherapy: progress and challenges.

التفاصيل البيبلوغرافية
العنوان: Chimeric antigen receptor-engineered T cells for cancer immunotherapy: progress and challenges.
المؤلفون: Han EQ; Drexel University College of Medicine, Philadelphia, PA 19129, USA., Li XL, Wang CR, Li TF, Han SY
المصدر: Journal of hematology & oncology [J Hematol Oncol] 2013 Jul 08; Vol. 6, pp. 47. Date of Electronic Publication: 2013 Jul 08.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Review
اللغة: English
بيانات الدورية: Publisher: Biomed Central Country of Publication: England NLM ID: 101468937 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-8722 (Electronic) Linking ISSN: 17568722 NLM ISO Abbreviation: J Hematol Oncol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: [London] : Biomed Central, 2008-
مواضيع طبية MeSH: Immunotherapy, Adoptive/*methods , Neoplasms/*immunology , Neoplasms/*therapy , Receptors, Antigen, T-Cell/*immunology , T-Lymphocytes/*immunology, Animals ; Humans ; Neoplasms/drug therapy ; Receptors, Antigen, T-Cell/genetics ; Recombinant Fusion Proteins/genetics ; Recombinant Fusion Proteins/immunology
مستخلص: Recent years have witnessed much progress in both basic research and clinical trials regarding cancer immunotherapy with chimeric antigen receptor (CAR)-engineered T cells. The unique structure of CAR endows T cell tumor specific cytotoxicity and resistance to immunosuppressive microenvironment in cancers, which helps patients to better tackle the issue of immunological tolerance. Adoptive immunotherapy (AIT) using this supernatural T cell have gained momentum after decades of intense debates because of the promising results obtained from preclinical models and clinical trials. However, it is very important for us to evaluate thoroughly the challenges/obstacles before widespread clinical application, which clearly warrants more studies to improve our understanding of the mechanism underlying AIT. In this review, we focus on the critical issues related to the clinical outcomes of CAR-based adoptive immunotherapy and discuss the rationales to refine this new cancer therapeutic modality.
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المشرفين على المادة: 0 (Receptors, Antigen, T-Cell)
0 (Recombinant Fusion Proteins)
تواريخ الأحداث: Date Created: 20130709 Date Completed: 20140505 Latest Revision: 20211021
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC3706354
DOI: 10.1186/1756-8722-6-47
PMID: 23829929
قاعدة البيانات: MEDLINE