Evaluation of B-cell intracellular signaling by monitoring the PI3K-Akt axis in patients with common variable immunodeficiency and activated phosphoinositide 3-kinase delta syndrome

Cytometry B Clin Cytom. 2021 Jul;100(4):460-466. doi: 10.1002/cyto.b.21956. Epub 2020 Sep 22.

Abstract

Background: Primary antibody deficiencies (PADs) are characterized by hypogammaglobulinemia and impaired B-cell differentiation. Patients with common variable immunodeficiency (CVID) present severe reductions in at least 2 serum immunoglobulins and impaired terminal differentiation of B cells. Most patients with CVID do not appear to present monogenic defects. Activated phosphoinositide 3-kinase delta syndrome (APDS), caused by gain-of-function mutations in the PIK3CD gene (p110δ), can present in patients with a CVID-like phenotype. Memory B-cell differentiation requires the orchestrated activation of numerous intracellular signaling pathways, which promote transcriptional programs required for long-term B-cell survival. The aim of this study was to develop a flow cytometry assay to trace the PI3K-Akt-mTOR pathway, a critical component of B-cell homeostasis, and analyze its status in PADs.

Methods: We analyzed the intracellular expression of Akt and S6 by flow cytometry and their phosphorylation status in both baseline conditions and upon B-cell receptor activation with anti-IgM in various primary B-cell subsets of patients with CVID and APDS.

Results: B cells from CVID patients showed reduced phosphorylation in Akt and S6 proteins after anti-IgM stimulation. Constitutive high baseline B-cell levels of Akt and S6 phosphorylation in a patient with APDS were reduced once m-TOR inhibition therapy was initiated.

Conclusions: Intracellular flow cytometry can be routinely employed to explore alterations in the PI3K-Akt-mTOR pathway in B cells from patients with PADs. AKT and S6 phosphorylation levels are informative biomarkers that could be employed as mTOR inhibitors for monitoring therapies targeting this pathway.

Keywords: B cells; common variable immunodeficiency; flow cytometry; monitoring PI3K-Akt pathway; phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocyte Subsets / metabolism
  • B-Lymphocyte Subsets / pathology
  • B-Lymphocytes / pathology
  • Class I Phosphatidylinositol 3-Kinases / genetics*
  • Common Variable Immunodeficiency / diagnosis*
  • Common Variable Immunodeficiency / genetics
  • Common Variable Immunodeficiency / pathology
  • Flow Cytometry
  • Humans
  • Lymphocyte Activation / genetics
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphorylation / genetics
  • Primary Immunodeficiency Diseases / diagnosis*
  • Primary Immunodeficiency Diseases / genetics
  • Primary Immunodeficiency Diseases / pathology
  • Proto-Oncogene Proteins c-akt / genetics*
  • Ribosomal Protein S6 Kinases / genetics*
  • Signal Transduction / genetics
  • TOR Serine-Threonine Kinases / genetics

Substances

  • MTOR protein, human
  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CD protein, human
  • Proto-Oncogene Proteins c-akt
  • Ribosomal Protein S6 Kinases
  • TOR Serine-Threonine Kinases

Supplementary concepts

  • Activated PI3K-delta Syndrome