PD-1hiCXCR5- T peripheral helper cells promote B cell responses in lupus via MAF and IL-21

JCI Insight. 2019 Oct 17;4(20):e130062. doi: 10.1172/jci.insight.130062.

Abstract

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by pathologic T cell-B cell interactions and autoantibody production. Defining the T cell populations that drive B cell responses in SLE may enable design of therapies that specifically target pathologic cell subsets. Here, we evaluated the phenotypes of CD4+ T cells in the circulation of 52 SLE patients drawn from multiple cohorts and identified a highly expanded PD-1hiCXCR5-CD4+ T cell population. Cytometric, transcriptomic, and functional assays demonstrated that PD-1hiCXCR5-CD4+ T cells from SLE patients are T peripheral helper (Tph) cells, a CXCR5- T cell population that stimulates B cell responses via IL-21. The frequency of Tph cells, but not T follicular helper (Tfh) cells, correlated with both clinical disease activity and the frequency of CD11c+ B cells in SLE patients. PD-1hiCD4+ T cells were found within lupus nephritis kidneys and correlated with B cell numbers in the kidney. Both IL-21 neutralization and CRISPR-mediated deletion of MAF abrogated the ability of Tph cells to induce memory B cell differentiation into plasmablasts in vitro. These findings identify Tph cells as a highly expanded T cell population in SLE and suggest a key role for Tph cells in stimulating pathologic B cell responses.

Keywords: Adaptive immunity; Autoimmunity; Immunology; Lupus; T cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • B-Lymphocytes / immunology*
  • CD11c Antigen / metabolism
  • CRISPR-Cas Systems / genetics
  • Case-Control Studies
  • Cell Communication / drug effects
  • Cell Communication / genetics
  • Cell Communication / immunology
  • Cell Culture Techniques
  • Cell Separation
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Flow Cytometry
  • Gene Knockout Techniques
  • Humans
  • Interleukins / antagonists & inhibitors
  • Interleukins / metabolism*
  • Lupus Erythematosus, Systemic / blood
  • Lupus Erythematosus, Systemic / immunology*
  • Lymphocyte Activation / drug effects
  • Lymphocyte Activation / genetics
  • Male
  • Middle Aged
  • Programmed Cell Death 1 Receptor / metabolism
  • Proto-Oncogene Proteins c-maf / genetics
  • Proto-Oncogene Proteins c-maf / metabolism*
  • RNA-Seq
  • Receptors, CXCR5 / metabolism
  • T-Lymphocytes, Helper-Inducer / immunology*
  • T-Lymphocytes, Helper-Inducer / metabolism

Substances

  • CD11c Antigen
  • CXCR5 protein, human
  • Interleukins
  • MAF protein, human
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Proto-Oncogene Proteins c-maf
  • Receptors, CXCR5
  • interleukin-21