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Th1-like Plasmodium-Specific Memory CD4+ T Cells Support Humoral Immunity

  • Ryan A. Zander
  • , Rahul Vijay
  • , Angela D. Pack
  • , Jenna J. Guthmiller
  • , Amy C. Graham
  • , Scott E. Lindner
  • , Ashley M. Vaughan
  • , Stefan H.I. Kappe
  • , Noah S. Butler

Research output: Contribution to journalArticlepeer-review

Abstract

Effector T cells exhibiting features of either T helper 1 (Th1) or T follicular helper (Tfh) populations are essential to control experimental Plasmodium infection and are believed to be critical for resistance to clinical malaria. To determine whether Plasmodium-specific Th1- and Tfh-like effector cells generate memory populations that contribute to protection, we developed transgenic parasites that enable high-resolution study of anti-malarial memory CD4 T cells in experimental models. We found that populations of both Th1- and Tfh-like Plasmodium-specific memory CD4 T cells persist. Unexpectedly, Th1-like memory cells exhibit phenotypic and functional features of Tfh cells during recall and provide potent B cell help and protection following transfer, characteristics that are enhanced following ligation of the T cell co-stimulatory receptor OX40. Our findings delineate critical functional attributes of Plasmodium-specific memory CD4 T cells and identify a host-specific factor that can be targeted to improve resolution of acute malaria and provide durable, long-term protection against Plasmodium parasite re-exposure. Th1 CD4 T cells are widely described as terminally differentiated with a relatively reduced capacity to form memory or support humoral immunity. Using experimental malaria models, Zander et al. show that potent proliferative and B cell helper activity unexpectedly resides within the Plasmodium-specific Th1-like memory CD4 T cell compartment.

Original languageEnglish (US)
Pages (from-to)1839-1852
Number of pages14
JournalCell Reports
Volume21
Issue number7
DOIs
StatePublished - Nov 14 2017

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • General Biochemistry, Genetics and Molecular Biology

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