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

598
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.
598
Cancer Vaccines01:30

Cancer Vaccines

459
Cancer treatment vaccines are a rapidly evolving field that offers a promising approach to immunotherapy. Unlike traditional vaccines that prevent diseases, cancer treatment vaccines are designed to treat existing cancers by stimulating the immune system to recognize and attack cancer cells.
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
459

You might also read

Related Articles

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

Sort by
Same author

Humanized FLT3 mice display enhanced tissue engraftment and support HIV‑1 persistence and rebound.

bioRxiv : the preprint server for biology·2026
Same author

First-line dolutegravir/lamivudine penetrates lymph nodes and reduces HIV reservoirs comparably to triple therapy.

Research square·2026
Same author

HIV-1 envelope glycoprotein modulates CXCR4 clustering and dynamics on the T cell membrane.

eLife·2026
Same author

Long-term HIV-1 remission achieved through allogeneic haematopoietic stem cell transplant from a CCR5Δ32/Δ32 sibling donor.

Nature microbiology·2026
Same author

Innate antiviral and immune functions associated with the HIV reservoir decay after anti-PD-1 therapy.

Nature medicine·2026
Same author

Strategies to Minimize Time From HIV Acquisition to ART Initiation: The Barcelona Early-cART Program.

Open forum infectious diseases·2025

Related Experiment Video

Updated: Aug 5, 2025

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype
08:49

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype

Published on: March 18, 2020

11.2K

Opportunities for CAR-T Cell Immunotherapy in HIV Cure.

Gerard Campos-Gonzalez1, Javier Martinez-Picado1,2,3,4,5, Talia Velasco-Hernandez6,7

  • 1IrsiCaixa AIDS Research Institute, 08916 Badalona, Spain.

Viruses
|March 30, 2023
PubMed
Summary

Chimeric antigen receptor (CAR)-T cell therapy shows promise for treating HIV, building on its success in blood cancers. Challenges like viral escape and reservoir accessibility remain, but ongoing trials offer hope for a future cure.

Keywords:
CAR-T cellsHIVHIV reservoirchimeric antigen receptorimmunotherapylatency reversal agents

More Related Videos

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
09:56

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy

Published on: February 21, 2025

695
Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
12:55

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care

Published on: February 16, 2015

21.5K

Related Experiment Videos

Last Updated: Aug 5, 2025

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype
08:49

Transduction and Expansion of Primary T Cells in Nine Days with Maintenance of Central Memory Phenotype

Published on: March 18, 2020

11.2K
A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
09:56

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy

Published on: February 21, 2025

695
Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
12:55

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care

Published on: February 16, 2015

21.5K

Area of Science:

  • Immunology
  • Virology
  • Biotechnology

Background:

  • Chimeric antigen receptor (CAR)-T cell therapy is a successful treatment for blood cancers like leukemia.
  • CAR-T cells are being investigated for their potential to cure human immunodeficiency virus (HIV) infection.

Purpose of the Study:

  • To review the development and advantages of CAR-T cell therapy.
  • To identify and discuss the obstacles in applying CAR-T cell therapy to HIV.
  • To highlight promising results and future prospects.

Main Methods:

  • Review of existing literature on CAR-T cell technology and its application in HIV research.
  • Analysis of challenges including viral escape, CAR-T cell infectivity, and reservoir accessibility.
  • Evaluation of clinical trial outcomes and future therapeutic potential.

Main Results:

  • CAR-T technology has significant potential for HIV treatment, adapting from its success in hematologic malignancies.
  • Key challenges include viral escape, CAR-T cell infectivity, and reaching latent HIV reservoirs.
  • Clinical trials show promising results in overcoming some of these obstacles.

Conclusions:

  • CAR-T cell therapy is a developing strategy for HIV cure, despite significant hurdles.
  • Addressing viral escape, infectivity, and reservoir accessibility is crucial for therapeutic success.
  • Promising clinical trial data suggests a positive outlook for CAR-T cells in HIV treatment.