Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Tumor Immunotherapy01:27

Tumor Immunotherapy

1.6K
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
1.6K
Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

6.3K
Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
6.3K
Cell-mediated Immune Responses01:40

Cell-mediated Immune Responses

82.8K
Overview
82.8K
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

14.3K
T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
14.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Power of Presence.

Family medicine·2026
Same author

Germline determinants of toxicity and efficacy in patients with large B-cell lymphoma treated with CAR T-cell therapy.

Journal for immunotherapy of cancer·2025
Same author

Teaching Preclinical Medical Students Lifestyle Counseling Skills for Patients' Health Behavior Change.

MedEdPORTAL : the journal of teaching and learning resources·2024
Same author

Medical Error: Using Storytelling and Reflection to Impact Resident Error Response Factors.

MedEdPORTAL : the journal of teaching and learning resources·2024
Same author

Medical Error: Using Storytelling and Reflection to Impact Error Response Factors in Family Medicine Residents.

Journal of medical education and curricular development·2024
Same author

Effect of delayed cell infusion in patients with large B-cell lymphoma treated with chimeric antigen receptor T-cell therapy.

Haematologica·2023

Related Experiment Video

Updated: Dec 14, 2025

Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
09:34

Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography

Published on: February 17, 2022

3.6K

Recognizing and Grading CAR T-Cell Toxicities: An Advanced Practitioner Perspective.

Savannah Sievers1, Grace Watson2, Swapna Johncy2

  • 1Department of Physician Assistant Programs, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Frontiers in Oncology
|July 17, 2020
PubMed
Summary
This summary is machine-generated.

Chimeric antigen receptor (CAR) T-cell therapy offers new hope for B-cell malignancies but carries risks like cytokine release syndrome. Early recognition and management of these toxicities are crucial for patient safety and effective treatment.

Keywords:
CAR T-celladvanced practice providerscytokine release syndromedifferential diagnosisimmune effector cell-associated neurotoxicity

More Related Videos

Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells
09:28

Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells

Published on: February 2, 2013

15.5K
Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
06:51

Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy

Published on: December 17, 2019

15.7K

Related Experiment Videos

Last Updated: Dec 14, 2025

Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
09:34

Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography

Published on: February 17, 2022

3.6K
Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells
09:28

Quantitative High-throughput Single-cell Cytotoxicity Assay For T Cells

Published on: February 2, 2013

15.5K
Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy
06:51

Manufacturing Chimeric Antigen Receptor CAR T Cells for Adoptive Immunotherapy

Published on: December 17, 2019

15.7K

Area of Science:

  • Oncology
  • Immunotherapy
  • Cellular Therapy

Background:

  • Chimeric antigen receptor (CAR) T-cell therapy has revolutionized B-cell malignancy treatment.
  • Expansion of CAR T-cell therapy to new targets and solid tumors is anticipated.
  • CAR T-cell therapy presents unique, potentially fatal toxicities like cytokine release syndrome and neurotoxicity.

Purpose of the Study:

  • To highlight the evolving understanding of CAR T-cell therapy toxicities.
  • To emphasize the critical role of advanced practice providers in managing these toxicities.
  • To underscore the need for institutional adaptation in providing CAR T-cell therapy.

Main Methods:

  • Review of current literature and clinical practice guidelines for CAR T-cell therapy.
  • Analysis of toxicity profiles, including cytokine release syndrome and neurotoxicity.
  • Examination of institutional infrastructure and staffing models for safe patient care.

Main Results:

  • CAR T-cell therapy demonstrates significant efficacy in relapsed/refractory B-cell malignancies.
  • Cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome are key adverse events.
  • Effective management requires multidisciplinary collaboration and provider expertise.

Conclusions:

  • Managing CAR T-cell therapy toxicities is a dynamic and evolving process.
  • Advanced practice providers are integral to the multidisciplinary team for patient care.
  • Institutions must adapt to safely administer and monitor patients receiving CAR T-cell therapy.