Inherited defects in the complement system.

alternative classical complement deficiency inherited lectin pathways system

Journal

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
ISSN: 1399-3038
Titre abrégé: Pediatr Allergy Immunol
Pays: England
ID NLM: 9106718

Informations de publication

Date de publication:
01 2022
Historique:
revised: 28 07 2021
received: 17 06 2021
accepted: 06 08 2021
entrez: 26 1 2022
pubmed: 27 1 2022
medline: 1 4 2022
Statut: ppublish

Résumé

The complement system plays an essential role in both innate and adaptive immune responses. Any dysregulation in this system can disturb normal host defense and alter inflammatory response leading to both infections and autoimmune diseases. The complement system can be activated through three different pathways. Inherited complement deficiencies have been described for all complement components and their regulators. Despite being rare diseases, complement deficiencies are often severe, with a frequent onset during childhood. We provide an overview of clinical disorders related to these disorders and describe current diagnostic strategies required for their comprehensive characterization and management.

Identifiants

pubmed: 35080299
doi: 10.1111/pai.13635
pmc: PMC9544610
doi:

Substances chimiques

Complement System Proteins 9007-36-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

73-76

Informations de copyright

© 2022 The Authors. Pediatric Allergy and Immunology published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

Références

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pubmed: 35080299
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Auteurs

Lucia Leonardi (L)

Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.

Francesco La Torre (F)

Department of Pediatrics, Giovanni XXIII Pediatric Hospital, University of Bari, Bari, Italy.

Annarosa Soresina (A)

Unit of Pediatric Immunology, Pediatrics Clinic, University of Brescia, ASST Spedali Civili Brescia, Brescia, Italy.

Silvia Federici (S)

Division of Rheumatology, IRCCS, Ospedale Pediatrico Bambino Gesù, Rome, Italy.

Caterina Cancrini (C)

Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy.
Academic Department of Pediatrics, Immune, and Infectious Diseases Division, Research Unit of Primary Immunodeficiencies, Bambino Gesù, Children's Hospital, IRCCS, Rome, Italy.

Riccardo Castagnoli (R)

Department of Pediatrics, Pediatric Clinic, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.

Bianca Laura Cinicola (BL)

Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Stefania Corrente (S)

Division of Pediatrics, S. Camillo-Forlanini Hospital, Rome, Italy.

Giuliana Giardino (G)

Pediatric Section, Department of Translational Medical Sciences, Federico II University, Naples, Italy.

Vassilios Lougaris (V)

Department of Clinical and Experimental Sciences, Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, University of Brescia and ASST-Spedali Civili di Brescia, Brescia, Italy.

Stefano Volpi (S)

Center for Autoinflammatory Diseases and Immunodeficiency, IRCCS Istituto Giannina Gaslini, Università degli Studi di Genova, Genoa, Italy.

Gian Luigi Marseglia (GL)

Department of Pediatrics, Pediatric Clinic, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.

Fabio Cardinale (F)

Department of Pediatrics, Giovanni XXIII Pediatric Hospital, University of Bari, Bari, Italy.

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Classifications MeSH