Increase of follicular helper T cells skewed toward a Th1 profile in CVID patients with non-infectious clinical complications

Clin Immunol. 2018 Dec:197:130-138. doi: 10.1016/j.clim.2018.09.006. Epub 2018 Sep 13.

Abstract

Common variable immunodeficiency (CVID) is characterized by low levels of circulating immunoglobulins and defects in B cell maturation leading to an increased susceptibility to infections. Some patients develop complications such as autoimmune diseases, enteropathy, and lymphoproliferation, resulting in higher morbidity and mortality. Follicular helper T (Tfh) cells are specialized in helping B cell differentiation into Ig-producing cells. Three subsets have been described, namely non B-cell helper Tfh1 and the two B-helper cell subsets Tfh2 and Tfh17. We determined that circulating Tfh cells were elevated in CVID patients and skewed toward a Tfh1 profile. Interestingly, elevated levels of Tfh1 cells were significant only in patients harboring non-infectious complications regardless of the type of complication and inversely correlated with switched memory B cells. Moreover, CXCR3+ cells are increased in splenic CVID germinal centers. Our observations suggest that the altered balance in Tfh subsets in CVID is linked to a more severe disease.

Keywords: CVID; Follicular helper T cells; Non-infectious complications; Th1 profile.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Autoimmune Diseases / immunology
  • B-Lymphocytes / immunology*
  • Case-Control Studies
  • Common Variable Immunodeficiency / immunology*
  • Female
  • Germinal Center / cytology
  • Germinal Center / immunology
  • Humans
  • Immunologic Memory / immunology*
  • Intestinal Diseases / immunology
  • Lymphopoiesis / immunology
  • Lymphoproliferative Disorders / immunology
  • Male
  • Middle Aged
  • Receptors, CXCR3
  • Sarcoidosis / immunology
  • Spleen / cytology
  • Spleen / immunology
  • T-Lymphocytes, Helper-Inducer / immunology
  • Th1 Cells / immunology*
  • Th17 Cells / immunology
  • Th2 Cells / immunology

Substances

  • CXCR3 protein, human
  • Receptors, CXCR3