Κυριακή 20 Σεπτεμβρίου 2020

Primary immune regulatory disorders: a growing universe of immune dysregulation

Primary immune regulatory disorders: a growing universe of immune dysregulation: Purpose of review

Primary immune regulatory disorders (PIRD) are a growing subset of diseases referred to as inborn errors of immunity. Unlike classical primary immune deficiency disorders that typically present with severe, recurrent, or unusual infections, the clinical manifestations of PIRD are dominated by immune-mediated diseases (autoimmunity, autoinflammation/hyperinflammation, lymphoproliferation, malignancy, and severe atopy). This review introduces the concept of PIRD including clinical phenotypes, treatments, and new PIRD-associated gene defects.

Recent findings

The number of genetic defects associated with PIRD is rapidly growing. The identified genes often encode proteins that play critical roles in regulating the immune response to various triggers. Understanding the molecular mechanisms underlying PIRD has shed light on the clinical phenotypes and has helped to identify targeted therapies. In some cases, hematopoietic cell transplant (HCT) has been successfully employed as a cure.

Summary

It is important to recognize the broad clinical manifestations of PIRD as patients may have symptoms atypical of classical ‘immunodeficiency’. Because of their diverse immune dysregulation problems, they are often primarily managed by other subspecialists. Immunologists can help connect the diverse immune-mediated pathologies to a gene defect. This, in turn, can play a significant role in directing clinical management, selecting effective therapy, and deciding on appropriateness of HCT.

Correspondence to Alice Y. Chan, Division of Pediatric Allergy, Immunology, and BMT, Department of Pediatrics, University of California, San Francisco, 550 16th Street, San Francisco, CA 94143, USA. Tel: +1 415 476 2171; e-mail: alice.chan1@ucsf.edu

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.


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