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 Experiment Videos

Human virus-specific CD8+ T cells: diversity specialists.

Ester M M van Leeuwen1, Godelieve J de Bree, Ineke J M ten Berge

  • 1Department of Experimental Immunology, Academic Medical Center, Amsterdam, the Netherlands.

Immunological Reviews
|July 11, 2006
PubMed
Summary

Human CD8+ T-cell responses to viruses vary significantly. Some T cells rely on cytokines like interleukin-7 (IL-7) for survival, while others, particularly those targeting latent viruses like cytomegalovirus (CMV), require viral antigens.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Early intervention, lasting impact: benefits of early antiretroviral therapy and implications for posttreatment control.

Current opinion in HIV and AIDS·2026
Same author

Humoral and cellular immune response after COVID-19 vaccination in patients with sickle cell disease on hydroxyurea.

Blood advances·2026
Same author

HIV-specific CD8+ T-cell proliferative response 24 weeks after early antiretroviral therapy initiation is associated with the subsequent reduction in the viral reservoir.

eLife·2026
Same author

Humoral and cellular immune response after COVID-19 vaccination in patients with sickle cell disease on hydroxyurea.

Blood advances·2025
Same author

HIV-1 envelope trimer vaccine induces sex-associated differences in antibody responses: a phase 1 clinical trial.

Nature communications·2025
Same author

Treatment in acute HIV infection only temporarily preserves monocyte function: a comparative cohort study in adult males.

EBioMedicine·2025

Area of Science:

  • Immunology
  • Virology
  • Cellular Biology

Background:

  • Human CD8+ T-cell responses to viral infections exhibit significant functional diversity.
  • This functional variation impacts T-cell expansion, migration, maintenance, and effector functions, potentially reflecting immune system adaptations to specific pathogens.
  • Understanding these divergent responses is crucial for developing effective immunotherapies.

Purpose of the Study:

  • To review the functional diversity of human CD8+ T-cell responses to viruses.
  • To explore the distinct mechanisms governing the maintenance of T cells specific for cleared versus persistent viruses.
  • To discuss the role of functionally diverse CD8+ T cells in immunity against persistent viral infections.

Main Methods:

  • Longitudinal follow-up of individuals post-primary viral infection.

Related Experiment Videos

  • Analysis of T-cell homeostatic maintenance mechanisms, including cytokine and antigen dependence.
  • Characterization of T-cell effector properties, particularly in the context of latent herpesviruses like Epstein-Barr virus and cytomegalovirus (CMV).
  • Main Results:

    • Virus-specific CD8+ T cells develop divergently from initial effector pools.
    • T cells targeting cleared viruses often depend on interleukin-7 (IL-7) for homeostatic maintenance.
    • T cells targeting latent viruses, such as Epstein-Barr virus and cytomegalovirus (CMV), frequently lack IL-7 receptor alpha (IL-7Ralpha) and require viral antigens for persistence.
    • Cytomegalovirus (CMV) uniquely generates a large population of resting CD8+ T cells with constitutive cytolytic function.

    Conclusions:

    • Functional diversity in CD8+ T-cell responses is a key feature of human antiviral immunity.
    • Distinct mechanisms regulate the survival of T cells specific for cleared versus persistent viruses.
    • The unique properties of CMV-induced T cells may play a significant role in controlling persistent viral infections.