4.7 Article

Cytotoxicity of CD19-CAR-NK92 cells is primarily mediated via perforin/granzyme pathway

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Medicine, General & Internal

Second-Line Tisagenlecleucel or Standard Care in Aggressive B-Cell Lymphoma

M. R. Bishop et al.

Summary: Tisagenlecleucel did not demonstrate superiority over standard salvage therapy in this trial. Further studies are needed to evaluate which patients may benefit the most from each approach.

NEW ENGLAND JOURNAL OF MEDICINE (2022)

Article Medicine, General & Internal

Axicabtagene Ciloleucel as Second-Line Therapy for Large B-Cell Lymphoma

F. L. Locke et al.

Summary: This international phase 3 trial showed that axicabtagene ciloleucel therapy significantly improved event-free survival and response in patients with early relapsed or refractory large B-cell lymphoma compared to standard care, despite the expected high-grade toxic effects.

NEW ENGLAND JOURNAL OF MEDICINE (2022)

Review Immunology

All About (NK Cell-Mediated) Death in Two Acts and an Unexpected Encore: Initiation, Execution and Activation of Adaptive Immunity

Ariel Ramirez-Labrada et al.

Summary: In this article, the available experimental evidence on how NK cells kill target cells is reviewed and discussed, with a special focus on the different cell death modalities that have been found to be activated during NK cell-mediated cytotoxicity, including apoptosis and more inflammatory pathways like necroptosis and pyroptosis. Based on this new evidence, NK cell-induced cell death is proposed as a new regulatory mechanism linking innate immune response with the activation of tumor adaptive T cell responses.

FRONTIERS IN IMMUNOLOGY (2022)

Article Oncology

Boosting CAR T-cell responses in lymphoma by simultaneous targeting of CD40/4-1BB using oncolytic viral gene therapy

Jessica Wenthe et al.

Summary: LOAd703, an immunostimulatory oncolytic adenovirus, shows potential in enhancing anti-lymphoma immune responses and improving CAR T-cell therapy efficacy in B-cell lymphoma models. LOAd703-infected lymphoma cells can stimulate CAR T-cell functionality resulting in enhanced cytokine release, degranulation marker expression, and reduced inhibitory receptor expression, leading to increased lymphoma cell killing. Additionally, LOAd703-infected lymphoma cells upregulate secretion of chemokines essential for immune cell homing, facilitating enhanced CAR T-cell migration.

CANCER IMMUNOLOGY IMMUNOTHERAPY (2021)

Review Cell Biology

NK Cells Armed with Chimeric Antigen Receptors (CAR): Roadblocks to Successful Development

Ali Bashiri Dezfouli et al.

Summary: In recent years, cell-based immunotherapies using Chimeric Antigen Receptors (CARs) have shown promise in cancer treatment, with CD19 CAR-engineered T cells being most commonly used for hematological malignancies. However, challenges in clinical applications include side effects like cytokine release syndrome, neurological symptoms, and off-target effects, necessitating the development of safer and more potent technologies. Natural Killer (NK) cells have emerged as a promising alternative, being capable of CAR engineering and exhibiting specialized lytic mechanisms against virally infected and cancer cells.
Review Biotechnology & Applied Microbiology

Navigating CAR-T cells through the solid-tumour microenvironment

Andrew J. Hou et al.

Summary: CAR-T cells have limited efficacy in treating solid tumors, but various engineering strategies can overcome the obstacles posed by the tumor microenvironment, producing next-generation T cells with enhanced specificity and sustained effector function.

NATURE REVIEWS DRUG DISCOVERY (2021)

Review Cell & Tissue Engineering

CAR-engineered NK cells; a promising therapeutic option for treatment of hematological malignancies

Faroogh Marofi et al.

Summary: CAR-NK cells are safer and more efficient than CAR-T cells in treating tumors, especially hematological malignancies. NK cells can be effectively engineered to express CARs with substantial cytotoxic activity against both hematological and solid tumors.

STEM CELL RESEARCH & THERAPY (2021)

Article Genetics & Heredity

Secondary resistance to anti-EGFR therapy by transcriptional reprogramming in patient-derived colorectal cancer models

Deepak Vangala et al.

Summary: By testing in vivo selection of anti-EGFR SR tumors in CRC PDX models, researchers have revealed the molecular details of developing secondary resistance mechanisms in CRC, suggesting that anti-EGFR tolerant cells via transcriptional reprogramming may be a common cause. Successful treatment of secondary resistant xenograft tumors was achieved using tailored targeted therapies.

GENOME MEDICINE (2021)

Article Medicine, General & Internal

Use of CAR-Transduced Natural Killer Cells in CD19-Positive Lymphoid Tumors

Enli Liu et al.

NEW ENGLAND JOURNAL OF MEDICINE (2020)

Review Biochemistry & Molecular Biology

Mechanisms of Apoptosis Resistance to NK Cell-Mediated Cytotoxicity in Cancer

Christian Sordo-Bahamonde et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)

Article Medicine, General & Internal

KTE-X19 CAR T-Cell Therapy in Relapsed or Refractory Mantle-Cell Lymphoma

Michael Wang et al.

NEW ENGLAND JOURNAL OF MEDICINE (2020)

Review Medicine, General & Internal

CAR-NK cells: A promising cellular immunotherapy for cancer

Guozhu Xie et al.

EBIOMEDICINE (2020)

Article Biochemistry & Molecular Biology

Direct Tumor Killing and Immunotherapy through Anti-SerpinB9 Therapy

Liwei Jiang et al.

Review Biochemistry & Molecular Biology

Killing Mechanisms of Chimeric Antigen Receptor (CAR) T Cells

Mohamed-Reda Benmebarek et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)

Review Cell Biology

Mechanisms of natural killer cell-mediated cellular cytotoxicity

Isabel Prager et al.

JOURNAL OF LEUKOCYTE BIOLOGY (2019)

Article Medicine, General & Internal

Anti-BCMA CAR T-Cell Therapy bb2121 in Relapsed or Refractory Multiple Myeloma

Noopur Raje et al.

NEW ENGLAND JOURNAL OF MEDICINE (2019)

Article Immunology

NK cells switch from granzyme B to death receptor-mediated cytotoxicity during serial killing

Isabel Prager et al.

JOURNAL OF EXPERIMENTAL MEDICINE (2019)

Article Cell Biology

The tyrosine kinase inhibitor dasatinib acts as a pharmacologic on/off switch for CAR T cells

Katrin Mestermann et al.

SCIENCE TRANSLATIONAL MEDICINE (2019)

Review Biochemistry & Molecular Biology

Natural Killer Cells and Current Applications of Chimeric Antigen Receptor-Modified NK-92 Cells in Tumor Immunotherapy

Jianguang Zhang et al.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2019)

Review Oncology

Chimeric antigen receptor T-cell therapy - assessment and management of toxicities

Sattva S. Neelapu et al.

NATURE REVIEWS CLINICAL ONCOLOGY (2018)

Article Oncology

ErbB2/HER2-Specific NK Cells for Targeted Therapy of Glioblastoma

Congcong Zhang et al.

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2016)

Article Oncology

ErbB2/HER2-Specific NK Cells for Targeted Therapy of Glioblastoma

Congcong Zhang et al.

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2016)

Article Cell Biology

CD19-CAR engineered NK-92 cells are sufficient to overcome NK cell resistance in B-cell malignancies

Annette Romanski et al.

JOURNAL OF CELLULAR AND MOLECULAR MEDICINE (2016)

Article Medicine, Research & Experimental

CD19 CAR-T cells of defined CD4+: CD8+ composition in adult B cell ALL patients

Cameron J. Turtle et al.

JOURNAL OF CLINICAL INVESTIGATION (2016)

Article Oncology

MiR-30a-5p suppresses tumor growth in colon carcinoma by targeting DTL

Alexander Baraniskin et al.

CARCINOGENESIS (2012)

Article Oncology

Construction and Preclinical Evaluation of an Anti-CD19 Chimeric Antigen Receptor

James N. Kochenderfer et al.

JOURNAL OF IMMUNOTHERAPY (2009)

Review Immunology

Functions of natural killer cells

Eric Vivier et al.

NATURE IMMUNOLOGY (2008)

Article Immunology

Bystander macrophage apoptosis after Mycobacterium tuberculosis H37Ra infection

Deirdre M. Kelly et al.

INFECTION AND IMMUNITY (2008)