Despite disorganized synapse structure, Th2 cells maintain directional delivery of CD40L to antigen-presenting B

Jennifer L Gardell1, David C Parker1

  • 1Department of Molecular Microbiology and Immunology, Oregon Health & Science University, Portland, Oregon, United States of America.

Plos One
|October 13, 2017
PubMed

Insights

Distinct T cell structures do not impact T cell help. Th1 and Th2 cells, despite differing immunological synapse structures, equally deliver CD40 ligand (CD40L) and provide antigen-specific T cell help to B cells.

Area of Science:

  • Immunology
  • Cell Biology
  • Molecular Biology

Background:

  • T helper 1 (Th1) and T helper 2 (Th2) cells exhibit distinct immunological synapse structures upon recognizing peptide-MHC complexes.
  • The immunological synapse is crucial for directing effector molecule delivery, including cytokines, in helper T cells.
  • CD40 ligand (CD40L) is vital for T cell help in B cell antibody responses.

Purpose of the Study:

  • To investigate if the structural differences in Th1 and Th2 cell immunological synapses affect the delivery of T cell help.
  • To determine if synapse structure influences the delivery of CD40L and subsequent B cell responses.

Main Methods:

  • Incubation of Th1 and Th2 cells with antigen-presenting and bystander B cells.
  • Comparison of CD40L delivery and B cell responses between Th1 and Th2 cells.
  • Assessment of susceptibility to inhibition by anti-CD40L antibody.

Main Results:

  • Th1 and Th2 cells demonstrated comparable abilities in delivering CD40L to B cells.
  • Both cell types provided antigen-specific T cell help effectively, irrespective of synapse structure.
  • Inhibition of T cell help by anti-CD40L antibody affected both Th1 and Th2 cells similarly.

Conclusions:

  • Immunological synapse structure does not dictate the efficacy of CD40L delivery or T cell help.
  • Th1 and Th2 cells provide equivalent T cell help for B cell antibody responses.
  • The functional outcome of T cell help is conserved despite structural variations in the immunological synapse.

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