Fiche du document

Date

11 février 2021

Périmètre
Langue
Identifiants
Relations

Ce document est lié à :
Frontiers Research Topics

Collection

DOAB

Organisation

OAPEN


Mots-clés Und

R5-920 RC581-607


Citer ce document

Directory of Open Access Books, ID : 10670/1.xqgxng


Métriques


Partage / Export

Résumé 0

Plasma cells (PCs) are terminally differentiated B-cells producing large amounts of immunoglobulins (Ig). In humans, most of circulating Ig are produced by bone marrow plasma cells. PCs differentiate from activated naïve or memory B-cells usually activated by specific antigens. It is still controversial whether the regulation of PCs numbers and the “active” in vivo Ig diversity depend or not on non-specific reactivation of B-cells during infections. Depending on the stimulus (T-independent/T-dependent antigen, cytokines, partner cells) and B-cell types (naïve or memory, circulating or germinal center, lymph nodes or spleen, B1 or B2...), both the phenotype and isotype of PCs differ suggesting that PC diversity is either linked to B-cell diversity or to the type of stimulus or to both. Knowledge of the mechanisms supporting PC diversity has important consequences for the management of i) plasma cell neoplasia such as Multiple Myeloma and Waldenström's Macroglobulinemia, ii) vaccine protection against pathogens and iii) auto-immune diseases.

document thumbnail

Sur les mêmes sujets

Sur les mêmes disciplines

Exporter en