Clinical utility of measuring CD4

Autoimmunity Evans syndrome Immune dysregulation Primary immune regulatory disorder T follicular helper cells

Journal

Journal of autoimmunity
ISSN: 1095-9157
Titre abrégé: J Autoimmun
Pays: England
ID NLM: 8812164

Informations de publication

Date de publication:
05 Aug 2023
Historique:
received: 25 05 2023
revised: 23 06 2023
accepted: 11 07 2023
medline: 8 8 2023
pubmed: 8 8 2023
entrez: 7 8 2023
Statut: aheadofprint

Résumé

Mechanistic studies of autoimmune disorders have identified circulating T follicular helper (cTfh) cells as drivers of autoimmunity. However, the quantification of cTfh cells is not yet used in clinical practice due to the lack of age-stratified normal ranges and the unknown sensitivity and specificity of this test for autoimmunity. We enrolled 238 healthy participants and 130 patients with common and rare disorders of autoimmunity or autoinflammation. Patients with infections, active malignancy, or any history of transplantation were excluded. In 238 healthy controls, median cTfh percentages (range 4.8%-6.2%) were comparable among age groups, sexes, races, and ethnicities, apart from a significantly lower percentages in children less than 1 year of age (median 2.1%, CI: 0.4%-6.8, p < 0.0001). Among 130 patients with over 40 immune regulatory disorders, a cTfh percentage exceeding 12% had 88% sensitivity and 94% specificity for differentiating disorders with adaptive immune cell dysregulation from those with predominantly innate cell defects. This threshold had a sensitivity of 86% and specificity of 100% for active autoimmunity and normalized with effective treatment. cTfh percentages exceeding 12% distinguish autoimmunity from autoinflammation, thereby differentiating two endotypes of immune dysregulation with overlapping symptoms and different therapies.

Identifiants

pubmed: 37549449
pii: S0896-8411(23)00097-5
doi: 10.1016/j.jaut.2023.103088
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103088

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI007512
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest All authors declare that no conflict of interest exists.

Auteurs

Brenna LaBere (B)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Alan A Nguyen (AA)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Saddiq B Habiballah (SB)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.

Megan Elkins (M)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Juliet Imperial (J)

Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Betty Li (B)

Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Sridevi Devana (S)

Takeda, Cambridge, MA, USA.

Suraj Timilsina (S)

Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Spencer B Stubbs (SB)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Jill Joerger (J)

Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Janet Chou (J)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Craig D Platt (CD)

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA; Department of Laboratory Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: craig.platt@childrens.harvard.edu.

Classifications MeSH