Literature DB >> 31578576

CAR T cell therapy: A new era for cancer treatment (Review).

Rimjhim Mohanty1, Chitran Roy Chowdhury1, Solomon Arega1, Prakriti Sen1, Pooja Ganguly1, Niladri Ganguly1.   

Abstract

Cancer has recently been identified as the leading cause of mortality worldwide. Several conventional treatments and cytotoxic immunotherapies have been developed and made available to the market. Considering the complex behavior of tumors and the involvement of numerous genetic and cellular factors involved in tumorigenesis and metastasis, there is a need to develop a promising immunotherapy that targets tumors at both the cellular and genetic levels. Chimeric antigen receptor (CAR) T cell therapy has emerged as a novel therapeutic T cell engineering practice, in which T cells derived from patient blood are engineered in vitro to express artificial receptors targeted to a specific tumor antigen. These directly identify the tumor antigen without the involvement of the major histocompatibility complex. The use of this therapy in the last few years has been successful, with a reduction in remission rates of up to 80% for hematologic cancer, particularly for acute lymphoblastic leukemia (ALL) and non‑Hodgkin lymphomas, such as large B cell lymphoma. Recently, anti‑CD19 CAR therapy, or UCART19, has been shown to be efficacious in treating relapsed/refractory hematologic cancer. Several other cell surface tumor antigens, such as CD20 and CD22, found in the majority of leukemias and lymphomas are considered potential targets by pharmaceutical companies and research organizations, and trials have been ongoing in this direction. Although this therapeutic regimen is currently confined to treating hematologic cancer, the increasing involvement of several auxiliary techniques, such as bispecific CAR, Tan‑CAR, inhibitory‑CAR, combined antigens, the clustered regularly interspaced short palindromic repeats gene‑editing tool and nanoparticle delivery, may substantially improve its overall anticancer effects. CAR therapy has the potential to offer a rapid and safer treatment regime to treat non‑solid and solid tumors. The present review presents an insight into the advantages and the advances of CAR immunotherapy and presents the emerging discrepancy of CAR therapy over usual forms of therapy, such as chemotherapy and radiotherapy.

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Year:  2019        PMID: 31578576     DOI: 10.3892/or.2019.7335

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  40 in total

1.  Not the comfy chair! Cancer drugs that act against multiple active sites.

Authors:  Laurence Booth; Andrew Poklepovic; Paul Dent
Journal:  Expert Opin Ther Targets       Date:  2019-11-14       Impact factor: 6.902

Review 2.  The challenge of selecting tumor antigens for chimeric antigen receptor T-cell therapy in ovarian cancer.

Authors:  Haigang Ding; Juan Zhang; Feng Zhang; Yan Xu; Yijun Yu; Wenqing Liang; Qingping Li
Journal:  Med Oncol       Date:  2022-09-29       Impact factor: 3.738

3.  Retinoblastoma cell-derived Twist protein promotes regulatory T cell development.

Authors:  Ruishi Zhang; Yan-Nan Song; Xiaoyan Duo; Zhihong Guo; Yanhua Sun; Zhixiong Zhang; Yongtian Lu; Beiping Miao; Ping-Chang Yang; Guohui Nie
Journal:  Cancer Immunol Immunother       Date:  2020-10-27       Impact factor: 6.968

Review 4.  Cancer immunotherapies revisited: state of the art of conventional treatments and next-generation nanomedicines.

Authors:  Coral García-Fernández; Anna Saz; Cristina Fornaguera; Salvador Borrós
Journal:  Cancer Gene Ther       Date:  2021-04-09       Impact factor: 5.987

Review 5.  Nanomedicine-based cancer immunotherapy: recent trends and future perspectives.

Authors:  Vinoth-Kumar Lakshmanan; Shlok Jindal; Gopinath Packirisamy; Shreesh Ojha; Sen Lian; Ajeet Kaushik; Abdulqadir Ismail M Abdullah Alzarooni; Yasser Abdelraouf Farahat Metwally; Sadras Panchatcharam Thyagarajan; Young Do Jung; Salem Chouaib
Journal:  Cancer Gene Ther       Date:  2021-02-08       Impact factor: 5.987

Review 6.  Tumor immune microenvironment in head and neck cancers.

Authors:  Samantha M Y Chen; Alexandra L Krinsky; Rachel A Woolaver; Xiaoguang Wang; Zhangguo Chen; Jing H Wang
Journal:  Mol Carcinog       Date:  2020-02-03       Impact factor: 4.784

Review 7.  New Insights into the Pathogenesis of Systemic Mastocytosis.

Authors:  Zhixiong Li
Journal:  Int J Mol Sci       Date:  2021-05-05       Impact factor: 5.923

Review 8.  CAR T cells: Building on the CD19 paradigm.

Authors:  Anat Globerson Levin; Isabelle Rivière; Zelig Eshhar; Michel Sadelain
Journal:  Eur J Immunol       Date:  2021-08-02       Impact factor: 6.688

9.  Combining selective inhibitors of nuclear export (SINEs) with chimeric antigen receptor (CAR) T cells for CD19‑positive malignancies.

Authors:  Sanmei Wang; Leopold Sellner; Lei Wang; Tim Sauer; Brigitte Neuber; Wenjie Gong; Sophia Stock; Ming Ni; Hao Yao; Christian Kleist; Anita Schmitt; Carsten Müller-Tidow; Michael Schmitt; Maria-Luisa Schubert
Journal:  Oncol Rep       Date:  2021-06-24       Impact factor: 3.906

Review 10.  The mechanisms of action of Plasmodium infection against cancer.

Authors:  Xiaoping Chen; Li Qin; Wen Hu; Dickson Adah
Journal:  Cell Commun Signal       Date:  2021-07-09       Impact factor: 5.712

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