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

Accessory cell function of Th2 clones.

B D Evavold1, J Quintans

  • 1Department of Pathology, University of Chicago, IL 60637.

Journal of Immunology (Baltimore, Md. : 1950)
|September 15, 1989
PubMed
Summary
This summary is machine-generated.

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

CIITA promoter I CARD-deficient mice express functional MHC class II genes in myeloid and lymphoid compartments.

Genes and immunity·2012
Same author

Antimicrobial properties of porphyrins.

Expert opinion on investigational drugs·2001
Same author

DO11.10 and OT-II T cells recognize a C-terminal ovalbumin 323-339 epitope.

Journal of immunology (Baltimore, Md. : 1950)·2000
Same author

Down-regulation of ceramide production abrogates ionizing radiation-induced cytochrome c release and apoptosis.

Molecular pharmacology·2000
Same author

[Combined perioperative ultrafiltration in pediatric cardiac surgery. The preliminary results].

Revista espanola de cardiologia·2000
Same author

Cutting edge: dueling TCRs: peptide antagonism of CD4+ T cells with dual antigen specificities.

Journal of immunology (Baltimore, Md. : 1950)·1999
Same journal

The scaffolding protein AKAP79/150 shapes innate immune responses to allergen.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same journal

Optineurin restrains IL-17-associated neuroinflammation in trigeminal ganglia to preserve sensory function after ocular HSV-1 infection.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same journal

Crystal structure and immune single-cell atlas provide insights into the functional divergence of type I IFNs in fish.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same journal

Complement C3 deficiency increases the effector and cytotoxic functions of NK cells and suppresses tumor growth.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same journal

Increased Nur77 is disconnected from TCR affinity in insulin-specific Tregs.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same journal

FTR85 negatively regulates type I IFN antiviral signaling pathway by promoting K48-linked polyubiquitination of IRF3.

Journal of immunology (Baltimore, Md. : 1950)·2026
See all related articles

T helper 2 (Th2) cells, but not T helper 2 (Th2) cells, act as accessory cells. They activate splenic T cells to proliferate when combined with mitogens, independent of MHC restriction.

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • T helper (Th) cells play crucial roles in adaptive immunity.
  • Accessory cells (AC) are essential for T cell activation and proliferation.
  • Understanding the specific functions of Th cell subsets as AC is vital for immune response modulation.

Purpose of the Study:

  • To investigate the capacity of T helper clones to function as accessory cells.
  • To determine the role of different T helper cell subsets in activating naive splenic T cells.
  • To elucidate the mechanisms underlying T cell activation by accessory Th cells in the presence of mitogens.

Main Methods:

  • Costimulatory assays using cloned T helper cells and freshly isolated splenic T cells.
  • Utilizing various T cell mitogens, including Concanavalin A (Con A) and monoclonal antibodies (mAbs) against CD3, TCR, and Thy-1.

Related Experiment Videos

  • Analyzing dose-response curves and assessing the involvement of MHC restriction.
  • Investigating the proliferation of CD4+ and CD8+ splenic T cells using specific mAbs.
  • Main Results:

    • T helper cells secreting Interleukin-4 (IL-4), identified as Th2 clones, effectively functioned as accessory cells.
    • Th2 cells induced splenic T cell proliferation in the presence of mitogens, independent of MHC restriction.
    • The activation signal involved a single stimulator cell and was not dependent on CD4 or CD8 expression on the responding T cells.

    Conclusions:

    • Cloned Th2 cells possess accessory cell function.
    • Th2 cells, in conjunction with mitogens, can induce proliferation of naive splenic T cells.
    • This Th2-mediated activation is MHC-independent and involves a single stimulator cell interaction.