Literature DB >> 25371415

Chimeric antigen receptor T-cell therapy to target hematologic malignancies.

Saad Sirop Kenderian1, Marco Ruella2, Saar Gill3, Michael Kalos4.   

Abstract

Several decades of humoral immunotherapy using monoclonal antibodies and cellular immunotherapy using hematopoietic cell transplantation have recently culminated in a successful merger: the development and clinical application of genetically engineered antibody-T cell chimeras. Also known as chimeric antigen receptor T cells (CAR T cells), these entities combine the exquisite antigen specificity of antibodies with the polyfunctionality and potency of cellular immunity and are a prime example of the potential for synthetic biology to treat disease. CAR T cells overcome several of the biologic obstacles that have historically hampered immunotherapy while providing fundamental mechanistic insights into cellular immunology and revealing new challenges in genetic engineering and target selection. Results from early-phase CAR T-cell-based clinical trials demonstrate the significant potential for this approach to affect dramatic and complete clinical responses while revealing novel toxicities associated with activation of potent and specific antitumor immunity. ©2014 American Association for Cancer Research.

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Year:  2014        PMID: 25371415     DOI: 10.1158/0008-5472.CAN-14-1530

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  21 in total

Review 1.  Chimeric Antigen Receptor T Cells and Hematopoietic Cell Transplantation: How Not to Put the CART Before the Horse.

Authors:  Saad S Kenderian; David L Porter; Saar Gill
Journal:  Biol Blood Marrow Transplant       Date:  2016-09-13       Impact factor: 5.742

Review 2.  Clinically feasible approaches to potentiating cancer cell-based immunotherapies.

Authors:  V I Seledtsov; A G Goncharov; G V Seledtsova
Journal:  Hum Vaccin Immunother       Date:  2015       Impact factor: 3.452

Review 3.  Combination of celecoxib (Celebrex®) and CD19 CAR-redirected CTL immunotherapy for the treatment of B-cell non-Hodgkin's lymphomas.

Authors:  Tam Nm Dinh; Alexandra S Onea; Ali R Jazirehi
Journal:  Am J Clin Exp Immunol       Date:  2017-05-15

Review 4.  Engineering therapeutic T cells to suppress alloimmune responses using TCRs, CARs, or BARs.

Authors:  Antoine Sicard; Megan K Levings; David W Scott
Journal:  Am J Transplant       Date:  2018-04-21       Impact factor: 8.086

Review 5.  Next-Generation Chimeric Antigen Receptor T-Cell Therapy: Going off the Shelf.

Authors:  Marco Ruella; Saad S Kenderian
Journal:  BioDrugs       Date:  2017-12       Impact factor: 5.807

Review 6.  Minimal Residual Disease Monitoring in Adult ALL to Determine Therapy.

Authors:  Renato Bassan; Orietta Spinelli
Journal:  Curr Hematol Malig Rep       Date:  2015-06       Impact factor: 3.952

7.  GM-CSF inhibition reduces cytokine release syndrome and neuroinflammation but enhances CAR-T cell function in xenografts.

Authors:  Rosalie M Sterner; Reona Sakemura; Michelle J Cox; Nan Yang; Roman H Khadka; Cynthia L Forsman; Michael J Hansen; Fang Jin; Katayoun Ayasoufi; Mehrdad Hefazi; Kendall J Schick; Denise K Walters; Omar Ahmed; Dale Chappell; Tarek Sahmoud; Cameron Durrant; Wendy K Nevala; Mrinal M Patnaik; Larry R Pease; Karen E Hedin; Neil E Kay; Aaron J Johnson; Saad S Kenderian
Journal:  Blood       Date:  2018-11-21       Impact factor: 22.113

Review 8.  CD19-redirected chimeric antigen receptor-modified T cells: a promising immunotherapy for children and adults with B-cell acute lymphoblastic leukemia (ALL).

Authors:  Sarah K Tasian; Rebecca A Gardner
Journal:  Ther Adv Hematol       Date:  2015-10

Review 9.  IL-2 and Beyond in Cancer Immunotherapy.

Authors:  John M Wrangle; Alicia Patterson; C Bryce Johnson; Daniel J Neitzke; Shikhar Mehrotra; Chadrick E Denlinger; Chrystal M Paulos; Zihai Li; David J Cole; Mark P Rubinstein
Journal:  J Interferon Cytokine Res       Date:  2018-02       Impact factor: 2.607

10.  Novel Targeted Therapy for Precursor B Cell Acute Lymphoblastic Leukemia: anti-CD22 Antibody-MXD3 Antisense Oligonucleotide Conjugate.

Authors:  Noriko Satake; Connie Duong; Sakiko Yoshida; Michael Oestergaard; Cathy Chen; Rachael Peralta; Shuling Guo; Punit P Seth; Yueju Li; Laurel Beckett; Jong Chung; Jan Nolta; Nitin Nitin; Joseph M Tuscano
Journal:  Mol Med       Date:  2016-07-22       Impact factor: 6.354

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