The challenge of early diagnosis of autoimmune lymphoproliferative syndrome in children with suspected autoinflammatory/autoimmune disorders.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
02 02 2022
Historique:
received: 17 12 2020
revised: 12 04 2021
pubmed: 29 4 2021
medline: 11 3 2022
entrez: 28 4 2021
Statut: ppublish

Résumé

To test the usefulness of an extended panel of lymphocyte subsets in combination with Oliveira's diagnostic criteria for the identification of autoimmune lymphoproliferative syndrome (ALPS) in children referred to a paediatric rheumatology centre. Patients referred from 2015 to 2018 to our rheumatology unit for an autoimmune or autoinflammatory condition were retrospectively analysed. Oliveira's required criteria [chronic lymphoproliferation and elevated double-negative T (DNT)] were applied as first screening. Flow cytometry study included double-negative CD4-CD8-TCRαβ+ T lymphocytes (DNT), CD25+CD3+, HLA-DR+CD3+ T cells, B220+ T cells and CD27+ B cells. Data were analysed with a univariate logistic regression analysis, followed by a multivariate analysis. Sensitivity and specificity of the Oliveira's required criteria were calculated. A total of 264 patients were included in the study and classified as: (i) autoimmune diseases (n = 26); (ii) juvenile idiopathic arthritis (JIA) (35); (iii) monogenic systemic autoinflammatory disease (27); (iv) periodic fever, aphthous stomatitis, pharyngitis and adenitis syndrome (100); (v) systemic undefined recurrent fever (45); (vi) undetermined-systemic autoinflammatory disease (14); or (vii) ALPS (17). Oliveira's required criteria displayed a sensitivity of 100% and specificity of 79%. When compared with other diseases the TCRαβ+B220+ lymphocytes were significantly increased in ALPS patients. The multivariate analysis revealed five clinical/laboratory parameters positively associated to ALPS: splenomegaly, female gender, arthralgia, elevated DNT and TCRαβ+B220+ lymphocytes. Oliveira's required criteria are useful for the early suspicion of ALPS. TCRαβ+B220+ lymphocytes should be added in the diagnostic work-up of patients referred to the paediatric rheumatology unit for a suspected autoimmune or autoinflammatory condition, providing a relevant support in the early diagnosis of ALPS.

Identifiants

pubmed: 33909886
pii: 6257227
doi: 10.1093/rheumatology/keab361
doi:

Substances chimiques

Receptors, Antigen, T-Cell, alpha-beta 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

696-704

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Leonardo Oliveira Mendonça (L)

Center for Autoinflammatory Diseases and Immunodeficiencies, IRCCS G. Gaslini.

Caterina Matucci-Cerinic (C)

Clinic of Pediatrics and Rheumatology, IRCCS G. Gaslini and University of Genoa.
DINOGMI, University of Genoa.

Paola Terranova (P)

Hematology Unit, IRCCS G. Gaslini.

Federica Casabona (F)

DINOGMI, University of Genoa.

Francesca Bovis (F)

Department of Health Sciences (DISSAL), University of Genoa.

Roberta Caorsi (R)

Center for Autoinflammatory Diseases and Immunodeficiencies, IRCCS G. Gaslini.

Francesca Fioredda (F)

Hematology Unit, IRCCS G. Gaslini.

Elena Palmisani (E)

Hematology Unit, IRCCS G. Gaslini.

Alice Grossi (A)

Laboratory of Genetics and Genomics of Rare Diseases, IRCCS G. Gaslini, Genoa, Italy.

Daniela Guardo (D)

Hematology Unit, IRCCS G. Gaslini.

Marta Bustaffa (M)

Clinic of Pediatrics and Rheumatology, IRCCS G. Gaslini and University of Genoa.
DINOGMI, University of Genoa.

Stefano Volpi (S)

Center for Autoinflammatory Diseases and Immunodeficiencies, IRCCS G. Gaslini.
DINOGMI, University of Genoa.

Isabella Ceccherini (I)

Laboratory of Genetics and Genomics of Rare Diseases, IRCCS G. Gaslini, Genoa, Italy.

Angelo Ravelli (A)

Clinic of Pediatrics and Rheumatology, IRCCS G. Gaslini and University of Genoa.

Carlo Dufour (C)

Hematology Unit, IRCCS G. Gaslini.

Maurizio Miano (M)

Hematology Unit, IRCCS G. Gaslini.

Marco Gattorno (M)

Center for Autoinflammatory Diseases and Immunodeficiencies, IRCCS G. Gaslini.

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