CAR T-cell therapy: toxicity and the relevance of preclinical models.

Chimeric antigen receptor (CAR) T cells form part of a broad wave of immunotherapies that are showing promise in early phase cancer clinical trials. This clinical delivery has been based upon preclinical efficacy testing that confirmed the proof of principle of the therapy. However, CAR T-cell therapy does not exist alone as T cells are generally given in combination with patient preconditioning, most commonly in the form of chemotherapy, and may also include systemic cytokine support, both of which are associated with toxicity. Consequently, complete CAR T-cell therapy includes elements where the toxicity profile is well known, but also includes the CAR T cell itself, for which toxicity profiles are largely unknown. With recent reports of adverse events associated with CAR T-cell therapy, there is now concern that current preclinical models may not be fit for purpose with respect to CAR T-cell toxicity profiling. Here, we explore the preclinical models used to validate CAR T-cell function and examine their potential to predict CAR T-cell driven toxicities for the future.

[1]  林雨樵 Targeting Fibroblast Activation Protein in Tumor Stroma with Chimeric Antigen Receptor T Cells Can Inhibit Tumor Growth and Augment Host Immunity without Severe Toxicity , 2015 .

[2]  S. Grupp,et al.  Nature of Tumor Control by Permanently and Transiently Modified GD2 Chimeric Antigen Receptor T Cells in Xenograft Models of Neuroblastoma , 2014, Cancer Immunology Research.

[3]  S. Grupp,et al.  Engineered T cells for cancer therapy , 2014, Cancer Immunology, Immunotherapy.

[4]  C. Creighton,et al.  Closely related T-memory stem cells correlate with in vivo expansion of CAR.CD19-T cells and are preserved by IL-7 and IL-15. , 2014, Blood.

[5]  Marcela V Maus,et al.  Antibody-modified T cells: CARs take the front seat for hematologic malignancies. , 2014, Blood.

[6]  G. Ashton,et al.  Differential Role of Th1 and Th2 Cytokines in Autotoxicity Driven by CD19-Specific Second-Generation Chimeric Antigen Receptor T Cells in a Mouse Model , 2014, The Journal of Immunology.

[7]  Q. Shen,et al.  Humanized NOD-SCID IL2rg–/– mice as a preclinical model for cancer research and its potential use for individualized cancer therapies. , 2014, Cancer letters.

[8]  D. Teachey,et al.  Managing Cytokine Release Syndrome Associated With Novel T Cell-Engaging Therapies , 2014, Cancer journal.

[9]  Qing He,et al.  Efficacy and Toxicity Management of 19-28z CAR T Cell Therapy in B Cell Acute Lymphoblastic Leukemia , 2014, Science Translational Medicine.

[10]  M. Essand,et al.  Systemic treatment with CAR-engineered T cells against PSCA delays subcutaneous tumor growth and prolongs survival of mice , 2014, BMC Cancer.

[11]  C. June,et al.  Engineering T cells for cancer: our synthetic future , 2014, Immunological reviews.

[12]  S. Gottschalk,et al.  Design and development of therapies using chimeric antigen receptor‐expressing T cells , 2014, Immunological reviews.

[13]  H. Abken,et al.  Of CARs and TRUCKs: chimeric antigen receptor (CAR) T cells engineered with an inducible cytokine to modulate the tumor stroma , 2014, Immunological reviews.

[14]  S. Riddell,et al.  Design and implementation of adoptive therapy with chimeric antigen receptor‐modified T cells , 2014, Immunological reviews.

[15]  Michel Sadelain,et al.  PD-1– and CTLA-4–Based Inhibitory Chimeric Antigen Receptors (iCARs) Divert Off-Target Immunotherapy Responses , 2013, Science Translational Medicine.

[16]  S. Ghaem-Maghami,et al.  Preclinical In Vivo Modeling of Cytokine Release Syndrome Induced by ErbB-Retargeted Human T Cells: Identifying a Window of Therapeutic Opportunity? , 2013, The Journal of Immunology.

[17]  D. Gilham,et al.  Isolation of tumor antigen-specific single-chain variable fragments using a chimeric antigen receptor bicistronic retroviral vector in a Mammalian screening protocol. , 2013, Human gene therapy methods.

[18]  J. Spicer,et al.  Design of a phase I clinical trial to evaluate intratumoral delivery of ErbB-targeted chimeric antigen receptor T-cells in locally advanced or recurrent head and neck cancer. , 2013, Human gene therapy. Clinical development.

[19]  R. Stahel,et al.  Treatment of malignant pleural mesothelioma by fibroblast activation protein-specific re-directed T cells , 2013, Journal of Translational Medicine.

[20]  D. Gilham,et al.  Potential limitations of the NSG humanized mouse as a model system to optimize engineered human T cell therapy for cancer. , 2013, Human gene therapy methods.

[21]  Hao Liu,et al.  Antitumor effects of chimeric receptor engineered human T cells directed to tumor stroma. , 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

[22]  M. Smyth,et al.  Anti-PD-1 Antibody Therapy Potently Enhances the Eradication of Established Tumors By Gene-Modified T Cells , 2013, Clinical Cancer Research.

[23]  Matthew L Baker,et al.  TanCAR: A Novel Bispecific Chimeric Antigen Receptor for Cancer Immunotherapy , 2013, Molecular therapy. Nucleic acids.

[24]  P. Delvenne,et al.  Infusion of clinical‐grade enriched regulatory T cells delays experimental xenogeneic graft‐versus‐host disease , 2013, Transfusion.

[25]  S. Rosenberg,et al.  Immune targeting of fibroblast activation protein triggers recognition of multipotent bone marrow stromal cells and cachexia , 2013, The Journal of experimental medicine.

[26]  R. Vile,et al.  CARbodies: Human Antibodies Against Cell Surface Tumor Antigens Selected From Repertoires Displayed on T Cell Chimeric Antigen Receptors , 2013, Molecular therapy. Nucleic acids.

[27]  S. Rosenberg,et al.  Treating B-cell cancer with T cells expressing anti-CD19 chimeric antigen receptors , 2013, Nature Reviews Clinical Oncology.

[28]  Michel Sadelain,et al.  The basic principles of chimeric antigen receptor design. , 2013, Cancer discovery.

[29]  Qing He,et al.  CD19-Targeted T Cells Rapidly Induce Molecular Remissions in Adults with Chemotherapy-Refractory Acute Lymphoblastic Leukemia , 2013, Science Translational Medicine.

[30]  Michel Sadelain,et al.  Combinatorial antigen recognition with balanced signaling promotes selective tumor eradication by engineered T cells , 2012, Nature Biotechnology.

[31]  A. Biondi,et al.  Comparison of different suicide-gene strategies for the safety improvement of genetically manipulated T cells. , 2012, Human gene therapy methods.

[32]  C. Klebanoff,et al.  Paths to stemness: building the ultimate antitumour T cell , 2012, Nature Reviews Cancer.

[33]  A. Scott,et al.  Targeting of a conformationally exposed, tumor-specific epitope of EGFR as a strategy for cancer therapy. , 2012, Cancer research.

[34]  S. Eccles,et al.  Flexible Targeting of ErbB Dimers That Drive Tumorigenesis by Using Genetically Engineered T Cells , 2012, Molecular medicine.

[35]  F. Bushman,et al.  Decade-Long Safety and Function of Retroviral-Modified Chimeric Antigen Receptor T Cells , 2012, Science Translational Medicine.

[36]  Jinjuan Wang,et al.  CD20-specific adoptive immunotherapy for lymphoma using a chimeric antigen receptor with both CD28 and 4-1BB domains: pilot clinical trial results. , 2012, Blood.

[37]  D. Gilham,et al.  Targeted immunotherapy of cancer with CAR T cells: achievements and challenges , 2012, Cancer Immunology, Immunotherapy.

[38]  W. Wilson,et al.  B-cell depletion and remissions of malignancy along with cytokine-associated toxicity in a clinical trial of anti-CD19 chimeric-antigen-receptor-transduced T cells. , 2012, Blood.

[39]  M. Sang,et al.  MAGE-A family: attractive targets for cancer immunotherapy. , 2011, Vaccine.

[40]  Adrian P Gee,et al.  Inducible apoptosis as a safety switch for adoptive cell therapy. , 2011, The New England journal of medicine.

[41]  S. Rosenberg,et al.  Treating cancer with genetically engineered T cells. , 2011, Trends in biotechnology.

[42]  S. Grupp,et al.  Treatment of advanced leukemia in mice with mRNA engineered T cells. , 2011, Human gene therapy.

[43]  C. Ramos,et al.  Chimeric antigen receptor (CAR)-engineered lymphocytes for cancer therapy , 2011, Expert opinion on biological therapy.

[44]  C. Pui,et al.  The tumor lysis syndrome. , 2011, The New England journal of medicine.

[45]  S. Mather,et al.  Trafficking of CAR-Engineered Human T Cells Following Regional or Systemic Adoptive Transfer in SCID Beige Mice , 2011, Journal of Clinical Immunology.

[46]  J. Trapani,et al.  Tumor ablation by gene-modified T cells in the absence of autoimmunity. , 2010, Cancer research.

[47]  W. Wilson,et al.  Eradication of B-lineage cells and regression of lymphoma in a patient treated with autologous T cells genetically engineered to recognize CD19. , 2010, Blood.

[48]  B. Levine,et al.  Multiple injections of electroporated autologous T cells expressing a chimeric antigen receptor mediate regression of human disseminated tumor. , 2010, Cancer research.

[49]  Raymond Sawaya,et al.  Immunologic escape after prolonged progression-free survival with epidermal growth factor receptor variant III peptide vaccination in patients with newly diagnosed glioblastoma. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[50]  S. Rosenberg,et al.  Case report of a serious adverse event following the administration of T cells transduced with a chimeric antigen receptor recognizing ERBB2. , 2010, Molecular therapy : the journal of the American Society of Gene Therapy.

[51]  H. Abken,et al.  Building better chimeric antigen receptors for adoptive T cell therapy. , 2010, Current gene therapy.

[52]  S. Dovedi,et al.  Natural Expression of the CD19 Antigen Impacts the Long-Term Engraftment but Not Antitumor Activity of CD19-Specific Engineered T Cells , 2010, The Journal of Immunology.

[53]  P. Bugelski,et al.  Monoclonal antibody-induced cytokine-release syndrome , 2009, Expert review of clinical immunology.

[54]  J. Maher,et al.  CAR mechanics: driving T cells into the MUC of cancer. , 2009, Cancer research.

[55]  D. Gilham,et al.  The combination of cyclophosphamide and human T cells genetically engineered to target CD19 can eradicate established B‐cell lymphoma , 2008, British journal of haematology.

[56]  S. Muruganandan,et al.  Mice as Clinically Relevant Models for the Study of Cytochrome P450‐dependent Metabolism , 2008, Clinical pharmacology and therapeutics.

[57]  J. Hung,et al.  Differential expression profile of MAGE family in non-small-cell lung cancer. , 2007, Lung cancer.

[58]  S. Forman,et al.  Specific Recognition and Killing of Glioblastoma Multiforme by Interleukin 13-Zetakine Redirected Cytolytic T Cells , 2004, Cancer Research.

[59]  S. Langermann,et al.  Differential EphA2 epitope display on normal versus malignant cells. , 2003, Cancer research.

[60]  Cameron S. Osborne,et al.  LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1 , 2003, Science.

[61]  W. Zimmermann,et al.  Evaluation of a transgenic mouse model for anti-human CEA radioimmunotherapeutics. , 2002, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[62]  Z. Eshhar,et al.  Expression of immunoglobulin-T-cell receptor chimeric molecules as functional receptors with antibody-type specificity. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[63]  Yao-Tseng Chen,et al.  NY-ESO-1: review of an immunogenic tumor antigen. , 2006, Advances in cancer research.