Mechanisms of Disease in Pediatric Lymphocyte Disorders Caused by PI3K Gene Mutations
Primary
immunodeficiency diseases (PIDs) affect approximately 10 million people
worldwide and most commonly present in childhood as severe susceptibility to
infections. The broad objective of this
study is to expand on our discoveries of phosphoinositide 3-kinase (PI3K) gene
mutations in pediatric immunodeficiencies to better understand the mechanistic
basis of disease. We and others have described a novel PID caused by
heterozygous, gain-of-function mutations in either the catalytic (PIK3CD) or the regulatory (PIK3R1) subunit of the
leukocyte-restricted PI3Kd complex. This disorder has been called PASLI disease
(for PI3Kd-Activating
mutation causing Senescent T cells, Lymphadenopathy, and Immunodeficiency), or
Activated PI3Kd Syndrome (APDS) for
short. These mostly pediatric patients
exhibit recurrent sinopulmonary infections, susceptibility to herpesviruses and
lymphoma, as well as lymphadenopathy/splenomegaly. We will pursue two specific aims to achieve
our broad objective.
In
Aim 1, we will study the mechanistic basis of CD4 T cell lymphopenia in APDS
patients by examining patient samples to investigate readouts of T cell
development/production, responses to growth cytokines, as well as cell death. Since CD4 T cells are “helper
cells” that orchestrate the adaptive immune response, a clearer
understanding of CD4 T cell pathology in this disorder could elucidate the
defects in other lymphocyte subsets (namely, CD8 T cells and B cells).
In
Aim 2, we will further investigate the role for PI3K and related genes in
pediatric immune disorders by performing whole-exome sequencing and genomic
analysis of undiagnosed PID patients. We
have succeeded in identifying novel PI3K gene defects in a proof-of-concept
study and aim to expand this approach and couple with rigorous mechanistic
studies. These efforts will provide
fundamental insights that inform precision therapies targeting PI3K or related
pathways that may be applied not only to these rare disorders but also more
broadly in common childhood diseases of immunity or autoimmunity.