Literature DB >> 32017223

Immunodeficiency and disorders of immune dysregulation.

Ottavia Maria Delmonte1.   

Abstract

The spectrum of clinical features associated with primary immune deficiency disorders (PIDs) has broadened due to the recent identification of many novel causative genes. Patients present with increased susceptibility to infections in addition to significant immune dysregulation, often leading to multiple autoimmunity, lymphoproliferation, and malignancy. Immunosuppressive treatment is often required but has to be weighed against augmented infectious risk. Recently, the improved molecular understanding of the mechanisms underlying many loss-of-function (LOF) and gain-of-function (GOF) genetic defects leading to PIDs has set the ground for the development of mechanism-based therapeutic strategies that target a specific cell function. This article describes the clinical and laboratory features of selected recently described PIDs associated with immune dysregulation and novel precision medicine strategies aimed to control the disease burden in affected patients.
© 2020 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd.

Entities:  

Keywords:  immune dysregulation; precision medicine; primary immunodeficiency diseases

Year:  2020        PMID: 32017223     DOI: 10.1111/pai.13163

Source DB:  PubMed          Journal:  Pediatr Allergy Immunol        ISSN: 0905-6157            Impact factor:   6.377


  2 in total

Review 1.  Future of Therapy for Inborn Errors of Immunity.

Authors:  Elena Perez
Journal:  Clin Rev Allergy Immunol       Date:  2022-01-12       Impact factor: 10.817

2.  Update in Primary Immunodeficiencies.

Authors:  Lucia Leonardi; Beatrice Rivalta; Caterina Cancrini; Elena Chiappini; Claudio Cravidi; Carlo Caffarelli; Sara Manti; Mauro Calvani; Alberto Martelli; Michele Miraglia Del Giudice; Marzia Duse; Gian Luigi Marseglia; Fabio Cardinale
Journal:  Acta Biomed       Date:  2020-09-15
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.