Defective formation of IgA memory B cells, Th1 and Th17 cells in symptomatic patients with selective IgA deficiency

ABSTRACT: Objective: Selective IgA deficiency (sIgAD) is the most common primary immunodeficiency in Western countries. Patients can suffer from recurrent infections and autoimmune diseases because of a largely unknown aetiology. To increase insights into the pathophysiology of the disease, we studi...

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Autores:

Moncada Vélez, Marcela
Franco Restrepo, José Luis
Franco Gallego, Alexander
Ahmadi, Fatemeh
Ash Dalm, Virgil
Lineth Rojas, Jessica
Orrego Arango, Julio César
Correa Vargas, Natalia
Hammarström, Lennart
Schreurs, Marco Wj
Dik, Willem A
van Hagen, P Martin
Boon, Louis
van Dongen, Jacques Jm
van der Burg, Mirjam
Pan Hammarström, Qiang
van Zelm, Menno C

Tipo de recurso:

Article of investigation

Fecha de publicación:

2020

Institución:

Universidad de Antioquia

Repositorio:

Repositorio UdeA

Idioma:

eng

OAI Identifier:

oai:bibliotecadigital.udea.edu.co:10495/40528

Acceso en línea:

https://hdl.handle.net/10495/40528

Palabra clave:

Células B de Memoria
Memory B Cells
Células TH1
Th1 Cells
Células Th17
Th17 Cells
Inmunoglobulina A
Immunoglobulin A
Citocinas
Cytokines
Deficiencia de IgA
IgA Deficiency
https://id.nlm.nih.gov/mesh/D000091245
https://id.nlm.nih.gov/mesh/D018417
https://id.nlm.nih.gov/mesh/D058504
https://id.nlm.nih.gov/mesh/D007070
https://id.nlm.nih.gov/mesh/D016207
https://id.nlm.nih.gov/mesh/D017098

Rights

openAccess

License

http://creativecommons.org/licenses/by/2.5/co/