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

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 studied memory...

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Detaylı Bibliyografya
Yayımlandı:Clin Transl Immunology
Asıl Yazarlar: Grosserichter‐Wagener, Christina, Franco‐Gallego, Alexander, Ahmadi, Fatemeh, Moncada‐Vélez, Marcela, Dalm, Virgil ASH, Rojas, Jessica Lineth, Orrego, 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, Franco, José L, van Zelm, Menno C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2020
Konular:
Short Communication
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7190975/
https://ncbi.nlm.nih.gov/pubmed/32355559
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cti2.1130
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