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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d7481a6cda3b47a693f06a960e2f80f0

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

About this item

Full title

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

Publisher

Australia: John Wiley & Sons, Inc

Journal title

Clinical & translational immunology, 2020-05, Vol.9 (5), p.e1130-n/a

Language

English

Formats

Publication information

Publisher

Australia: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

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 B and T cells and cytokine concentrations in per...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_d7481a6cda3b47a693f06a960e2f80f0

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d7481a6cda3b47a693f06a960e2f80f0

Other Identifiers

ISSN

2050-0068

E-ISSN

2050-0068

DOI

10.1002/cti2.1130

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