The Effects of Stimulation with PMA/Ionomycin on CD4+ T Cell Proliferation and Surface CD4 Molecule Modulation of Patients with LRBA Deficiency and CVID with the Unsolved Genetic Defect

Endocr Metab Immune Disord Drug Targets. 2022;22(5):539-544. doi: 10.2174/1871530321666211209162834.

Abstract

Background: Common variable immunodeficiency (CVID) is the most prevalent symptomatic primary immunodeficiencies. LPS-responsive beige-like anchor protein (LRBA) deficiency is a combined immunodeficiency characterized by a CVID-like phenotype. Affected patients by LRBA and CVID present a wide range of clinical manifestations, including hypogammaglobulinemia, recurrent infections, autoimmunity, as well as T cell abnormality.

Methods: The study population comprised of patients with CVID (n=10), LRBA deficiency (n=11), and healthy controls (n=12). CD4+ T cell frequency and CD4 MFI (mean fluorescence intensity) were evaluated using flow cytometry before and after stimulation with PMA/ION.

Results: The frequencies of CD4+ T cells were significantly lower in patients with LRBA deficiency than in HCs before and after treatment. In the unstimulated state, the CD4+ T cells frequency in CVID patients was significantly lower than in HCs. There were no statistically significant differences between patients and healthy individuals in CD4+ T cell proliferation. Compared to HCs, LRBA and CVID patients showed a lower CD4 MFI in unstimulated conditions. Furthermore, CD4 MFI decreased in both patients and the control group following activation.

Conclusion: Despite the reported decrease in CD4+ T cell frequency in patients with CVID and LRBA deficiency, our findings demonstrated that their CD4+ T cells have a normal proliferative response to stimuli similar to healthy individuals.

Keywords: CD4+ T cell; Common variable immunodeficiency; LRBA deficiency; primary immunodeficiencies; proliferation; stimulation.

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • CD4 Antigens / metabolism
  • CD4-Positive T-Lymphocytes / metabolism
  • Cell Proliferation
  • Common Variable Immunodeficiency* / genetics
  • Humans
  • Ionomycin

Substances

  • Adaptor Proteins, Signal Transducing
  • CD4 Antigens
  • Ionomycin
  • LRBA protein, human