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

T-helper cells from naive to committed.

Armin Saalmüller1, Tobias Werner, Vicky Fachinger

  • 1Institute for Immunology, Federal Research Centre for Virus Diseases of Animals, P.O. Box 1149, Paul-Ehrlich-Strasse 28, 72076 Tübingen, Germany. armin.saalmueller@tue.bfav.de

Veterinary Immunology and Immunopathology
|June 20, 2002
PubMed
Summary

In pigs, naive CD4(+)CD8(-) T-helper cells mature into CD4(+)CD8alpha(+) memory cells. This CD4(+)CD8alpha(+) subpopulation is crucial for secondary immune responses, particularly against classical swine fever virus.

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

Recognising and mitigating LLM Pollution in online behavioural research.

Nature communications·2026
Same author

Multitargeted Aza-Arylcarboxamides for Neurodegenerative Diseases: Potent Histamine H<sub>3</sub> Receptor Ligands with Anticholinesterase and Metal-Chelating Activities.

ACS chemical neuroscience·2026
Same author

Investigating the functional capacity of porcine uterine natural killer cells during a porcine reproductive and respiratory syndrome virus infection of pregnant gilts.

Veterinary research·2025
Same author

Design, Synthesis, and Biological Evaluation of Novel Multitarget 7-Alcoxyamino-3-(1,2,3-triazole)-coumarins as Potent Acetylcholinesterase Inhibitors.

Pharmaceuticals (Basel, Switzerland)·2025
Same author

Targeting Histone H3K9 Methyltransferase G9a as a Potential Therapeutic Strategy for Neuropsychiatric Disorders.

Medicinal research reviews·2025
Same author

First in class pyrrolo[2,3-d]pyrimidine derivatives fused to fluorobenzylpiperidines as dual ligands of acetylcholinesterase and histamine H<sub>3</sub> receptor.

Archiv der Pharmazie·2025

Area of Science:

  • Immunology
  • Swine immunology
  • Cellular immunology

Background:

  • T-helper cells are vital for adaptive immunity in pigs.
  • Two distinct CD4(+) T-helper cell subpopulations exist in extra-thymic compartments.
  • These subpopulations differ in surface antigen expression, including CD8alpha and MHCII.

Purpose of the Study:

  • To investigate the differentiation and function of porcine T-helper cell subpopulations.
  • To identify the phenotype of naive and memory T-helper cells in swine.
  • To understand the role of CD4(+)CD8alpha(+) T-cells in secondary immune responses.

Main Methods:

  • In vitro immune reactions stimulated with Staphylococcal Enterotoxin B (SEB).
  • Analysis of surface antigen expression (CD4, CD8alpha, MHCII, CD45RC) on T-helper cells.

Related Experiment Videos

  • Secondary in vitro immune response against classical swine fever virus.
  • Main Results:

    • Primary immune response mainly involves the CD4(+)CD8(-) subpopulation (naive T-helper cells).
    • Activation leads to CD8alpha and MHCII expression and CD45RC down-regulation, resembling the CD4(+)CD8alpha(+) subpopulation.
    • Only the CD4(+)CD8alpha(+) T-helper subpopulation responded in secondary immune assays, indicating it harbors memory cells.

    Conclusions:

    • Naive CD4(+)CD8(-)MHCII(-) porcine T-helper cells undergo extra-thymic maturation.
    • This maturation results in committed CD4(+)CD8alpha(+)MHCII(+) T-helper cells.
    • The CD4(+)CD8alpha(+) subpopulation represents T-helper memory cells in swine.