Germinal Centre Shutdown.
Animals
Antibodies
/ immunology
Antigen Presentation
Apoptosis
B-Lymphocyte Subsets
/ cytology
Cell Division
Cell Lineage
Cytokines
/ physiology
Dendritic Cells, Follicular
/ immunology
Feedback, Physiological
Gene Rearrangement, B-Lymphocyte
Germinal Center
/ cytology
Humans
Infections
/ immunology
Lymphoma, B-Cell
/ immunology
Lymphopoiesis
Macrophages
/ immunology
Memory B Cells
/ metabolism
Mice
Models, Immunological
Plasma Cells
/ cytology
Vaccines
B cell lymphoma
antibody responses
chronic germinal centres
ectopic germinal centres
germinal centre shutdown
vaccination
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
04
05
2021
accepted:
24
06
2021
entrez:
26
7
2021
pubmed:
27
7
2021
medline:
21
12
2021
Statut:
epublish
Résumé
Germinal Centres (GCs) are transient structures in secondary lymphoid organs, where affinity maturation of B cells takes place following an infection. While GCs are responsible for protective antibody responses, dysregulated GC reactions are associated with autoimmune disease and B cell lymphoma. Typically, 'normal' GCs persist for a limited period of time and eventually undergo shutdown. In this review, we focus on an important but unanswered question - what causes the natural termination of the GC reaction? In murine experiments, lack of antigen, absence or constitutive T cell help leads to premature termination of the GC reaction. Consequently, our present understanding is limited to the idea that GCs are terminated due to a decrease in antigen access or changes in the nature of T cell help. However, there is no direct evidence on which biological signals are primarily responsible for natural termination of GCs and a mechanistic understanding is clearly lacking. We discuss the present understanding of the GC shutdown, from factors impacting GC dynamics to changes in cellular interactions/dynamics during the GC lifetime. We also address potential missing links and remaining questions in GC biology, to facilitate further studies to promote a better understanding of GC shutdown in infection and immune dysregulation.
Identifiants
pubmed: 34305944
doi: 10.3389/fimmu.2021.705240
pmc: PMC8293096
doi:
Substances chimiques
Antibodies
0
Cytokines
0
Vaccines
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
705240Informations de copyright
Copyright © 2021 Arulraj, Binder, Robert and Meyer-Hermann.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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