Innate B Cells: the Archetype of Protective Immune Cells.


Journal

Clinical reviews in allergy & immunology
ISSN: 1559-0267
Titre abrégé: Clin Rev Allergy Immunol
Pays: United States
ID NLM: 9504368

Informations de publication

Date de publication:
Feb 2020
Historique:
pubmed: 12 6 2019
medline: 29 9 2020
entrez: 12 6 2019
Statut: ppublish

Résumé

The innate B cell (IBC) population is heterogeneous and involved in the primary immune response. IBC functions include a high ability to produce natural antibodies with IgM isotype, the elimination of apoptotic cells, and a capacity to be cognate help to T cells. Among IBC subsets, B-1 cells and marginal zone B cells are the main producers of IgM, act as rapid immune responders that may relocate to follicular lymphoid and differentiate to cytokine and antibody-secreting cells shortly after infection. IBCs functions are highly dependent on their localization site and the nature of their B cell receptor repertoire, suggesting a high plasticity range of different immune responses. In this review, we will describe the nature and functions of the different innate-like B cell subsets, first in mice and then in humans. Besides this, we will emphasize the strong ability of these cells to undertake different protective functions from the first line of defense against pathogens to the regulatory role of the broader immune response.

Identifiants

pubmed: 31183788
doi: 10.1007/s12016-019-08748-7
pii: 10.1007/s12016-019-08748-7
doi:

Substances chimiques

Cytokines 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

92-106

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Auteurs

Alexis Grasseau (A)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Marina Boudigou (M)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Laëtitia Le Pottier (L)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Nedra Chriti (N)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Divi Cornec (D)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Jacques-Olivier Pers (JO)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.

Yves Renaudineau (Y)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France.
Laboratory of Immunology and Immunotherapy, CHU Brest, Brest, France.

Sophie Hillion (S)

UMR1227, Lymphocytes B et Autoimmunité, Université de Brest, INSERM, CHU de Brest, BP824, F29609, Brest, France. sophie.hillion@univ-brest.fr.
Laboratory of Immunology and Immunotherapy, CHU Brest, Brest, France. sophie.hillion@univ-brest.fr.

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