Targeted pharmacologic immunomodulation for inborn errors of immunity.
Keith A SaccoMichael StackLuigi D NotarangeloPublished in: British journal of clinical pharmacology (2020)
Inborn errors of immunity consist of over 400 known single gene disorders that may manifest with infection susceptibility, autoimmunity, autoinflammation, hypersensitivity and cancer predisposition. Most patients are treated symptomatically with immunoglobulin replacement, prophylactic antimicrobials or broad immunosuppression pertaining to their disease phenotype. Other than haematopoietic stem cell transplantation, the aforementioned treatments do little to alter disease morbidity or mortality. Further, many patients may not be transplant candidates. In this review, we describe monogenic disorders affecting leucocyte migration, disorders of immune synapse formation and dysregulation of immune cell signal transduction. We highlight the use of off-label small molecules and biologics mechanistically targeted to altered disease pathophysiology of such diseases.
Keyphrases
- end stage renal disease
- stem cell transplantation
- newly diagnosed
- ejection fraction
- chronic kidney disease
- emergency department
- gene expression
- peritoneal dialysis
- cardiovascular disease
- squamous cell carcinoma
- type diabetes
- drug delivery
- patient reported outcomes
- adverse drug
- genome wide identification
- genome wide analysis