Figure 2 Approaches to improve CAR-T-cell therapy

Slides:



Advertisements
Similar presentations
Basic Immunology of the Mouse (and Human) Nicholas P. Restifo, MD October 19, 2015.
Advertisements

chimeric antigen receptor T-cell therapy for ALL
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 1 CTLA-4 and PD-1–PD-L1 immune checkpoints
Figure 1 Concept of the therapeutic index
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Discussion Outline Cells of the Immune System.
Figure 1 Cellular processes involved in cancer development
Figure 2 Immune-escape mechanisms of CTCs in the peripheral blood
Figure 5 Schematic illustration of different clinical trial designs
Figure 1 Generations of cancer vaccine antigens
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Figure 1 Immunomodulatory monoclonal antibodies and armoured chimeric antigen receptor (CAR) T cells overcome immune suppression Figure 1 | Immunomodulatory.
Figure 2 Neoantigen presentation in the tumour microenvironment
Figure 1 Four nodes to target when inducing anti-tumour immunity
Scratching the Surface of Immunotherapeutic Targets in Neuroblastoma
Figure 3 Intracranial targeting of high-grade gliomas
Figure 2 Three-step approach to the assessment and management
Figure 1 Current treatments for PNETs
Research Techniques Made Simple: CAR T-Cell Therapy
Figure 1 Chimeric antigen receptor (CAR) structures
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Antibody-modified T cells: CARs take the front seat for hematologic malignancies by Marcela V. Maus, Stephan A. Grupp, David L. Porter, and Carl H. June.
Figure 7 Clinical options for HCC therapy
Will Engineered T Cells Expressing CD20 scFv Eradicate Melanoma?
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Nat. Rev. Clin. Oncol. doi: /nrclinonc
CAR T cell therapy—principle and clinical trial overview
Figure 5 Classification of immunotherapies
CAR T cell therapy—principle and clinical trial overview
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Figure 1 CAR-T-cell design
Nat. Rev. Gastroenterol. Hepatol. doi: /nrgastro
Figure 2 Co-stimulatory receptors as immunomodulatory targets
Figure 4 Combination immunotherapeutic approaches with imatinib
Figure 2 The association between CD8+ T‑cell density of the tumour
Figure 6 Combination therapy for HCC
Figure 1 Clinical case study
Nat. Rev. Urol. doi: /nrurol
Scratching the Surface of Immunotherapeutic Targets in Neuroblastoma
Figure 4 Approaches to targeting inhibitory immune receptors
Nat. Rev. Urol. doi: /nrurol
Figure 4 Macrophage-targeting antitumour treatment approaches
Nat. Rev. Urol. doi: /nrurol
Nat. Rev. Urol. doi: /nrurol
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 3 Drug cycling with collateral sensitivity
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 2 Emerging models of antibody-mediated rejection (ABMR) and
Figure 3 Clinical trial design in charged-particle therapy (CPT)
Figure 5 The mechanism underlying epithelial-to-mesenchymal
Nat. Rev. Rheumatol. doi: /nrrheum
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 1 The role of CTLA4 and PD1 in T cell activation
Figure 2 Site of action of checkpoint inhibitors and agonists being
Figure 2 Effects of imatinib on components of the anticancer immunosurveillance system Figure 2 | Effects of imatinib on components of the anticancer immunosurveillance.
Figure 1 The VEGF family of growth factors
Nat. Rev. Endocrinol. doi: /nrendo
Figure 1 Mechanisms of oncolytic-virus-based cancer therapy
Nat. Rev. Rheumatol. doi: /nrrheum
Figure 3 Tumours secrete factors that cause systemic immunosuppression
Figure 1 Mechanisms of action of immunotherapy modalities
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Nat. Rev. Urol. doi: /nrurol
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 3 Determination of the primary site
Distribution of immune checkpoint in tumor cells and immune microenvironment. CTLA-4, cytotoxic T lymphocyte antigen-4; MHC, major histocompatibility complex;
Toxicity and management in CAR T-cell therapy
(A) Lymph node priming phase: recognition of major histocompatibility complex (MHC) by T-cell receptor (TCR), coactivating CD 28/B7 pathway activation.
Human cancer immunotherapy strategies targeting B7-H3 A, blockade of B7-H3 with blocking mAbs neutralizes inhibitory signaling in its unidentified receptor(s)
Presentation transcript:

Figure 2 Approaches to improve CAR-T-cell therapy Figure 2 | Approaches to improve CAR-T-cell therapy. An overview of the improvements to chimeric antigen receptor (CAR)-T-cell therapy is shown, and clinical trials testing those strategies are indicated in the legend. a | Engineered CAR T cells that secrete pro-inflammatory cytokines (armoured CAR T cells; NCT02498912)137. b | Dual receptor expression to target tumour cells and convert tumour-derived cytokines into T-cell activators (NCT01818323)164. c | Using natural killer (NK)-cell-based recognition domains, such as NKG2-D, in CARs (NCT02203825)148. d | Combination therapy with monoclonal antibodies (mAb) targeting immune-checkpoint inhibitory receptors to relieve immunosuppression (NCT00586391)154. e | Infusion of two populations of CAR T cells to eradicate B cells and enable increased persistence of tumour-specific CAR T cells by preventing antibody responses against their foreign antigen components (NCT02465983)156. f | Targeting the tumour vasculature with CAR T cells, such as VEGFR-2-specific CAR T cells NCT01218867160. 4αβ, 4αβ chimeric cytokine receptor; CTLA-4, cytotoxic T-lymphocyte-associate antigen-4; T1E28z, T1E28z chimeric antigen receptor; VEGFR-2, vascular endothelial growth factor receptor 2. Jackson, H. J. et al. (2016) Driving CAR T‑cells forward Nat. Rev. Clin. Oncol. doi:10.1038/nrclinonc.2016.36