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Biology of Germinal Center B Cells Relating to Lymphomagenesis
The germinal center (GC) reaction is a key feature of adaptive humoral immunity. GCs represent the site where mature B cells refine their B-cell receptor (BCR) and are selected based on the newly acquired affinity for the antigen. In the GC, B cells undergo multiple cycles of proliferation, BCR remo...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams & Wilkins
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171379/ https://www.ncbi.nlm.nih.gov/pubmed/34095765 http://dx.doi.org/10.1097/HS9.0000000000000582 |
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author | Basso, Katia |
author_facet | Basso, Katia |
author_sort | Basso, Katia |
collection | PubMed |
description | The germinal center (GC) reaction is a key feature of adaptive humoral immunity. GCs represent the site where mature B cells refine their B-cell receptor (BCR) and are selected based on the newly acquired affinity for the antigen. In the GC, B cells undergo multiple cycles of proliferation, BCR remodeling by immunoglobulin somatic hypermutation (SHM), and affinity-based selection before emerging as effector memory B cells or antibody-secreting plasma cells. At least 2 histologically and functionally distinct compartments are identified in the GC: the dark zone (DZ) and the light zone (LZ). The proliferative burst and immunoglobulin remodeling by SHM occur prevalently in the DZ compartment. In the LZ, GC B cells undergo an affinity-based selection process that requires the interaction with the antigen and accessory cells. GC B cells are also targeted by class switch recombination, an additional mechanism of immunoglobulin remodeling that ensures the expression of diverse isotype classes. These processes are regulated by a complex network of transcription factors, epigenetic modifiers, and signaling pathways that act in concert with mechanisms of intra-GC B-cell trafficking. The same mechanisms underlying the unique ability of GC B cells to generate high affinity antibodies and ensure immunological memory are hijacked during lymphomagenesis and become powerful weapons for malignant transformation. This review will summarize the main processes and transcriptional networks that drive GC B-cell development and are relevant for human B-cell lymphomagenesis. |
format | Online Article Text |
id | pubmed-8171379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-81713792021-06-03 Biology of Germinal Center B Cells Relating to Lymphomagenesis Basso, Katia Hemasphere Review The germinal center (GC) reaction is a key feature of adaptive humoral immunity. GCs represent the site where mature B cells refine their B-cell receptor (BCR) and are selected based on the newly acquired affinity for the antigen. In the GC, B cells undergo multiple cycles of proliferation, BCR remodeling by immunoglobulin somatic hypermutation (SHM), and affinity-based selection before emerging as effector memory B cells or antibody-secreting plasma cells. At least 2 histologically and functionally distinct compartments are identified in the GC: the dark zone (DZ) and the light zone (LZ). The proliferative burst and immunoglobulin remodeling by SHM occur prevalently in the DZ compartment. In the LZ, GC B cells undergo an affinity-based selection process that requires the interaction with the antigen and accessory cells. GC B cells are also targeted by class switch recombination, an additional mechanism of immunoglobulin remodeling that ensures the expression of diverse isotype classes. These processes are regulated by a complex network of transcription factors, epigenetic modifiers, and signaling pathways that act in concert with mechanisms of intra-GC B-cell trafficking. The same mechanisms underlying the unique ability of GC B cells to generate high affinity antibodies and ensure immunological memory are hijacked during lymphomagenesis and become powerful weapons for malignant transformation. This review will summarize the main processes and transcriptional networks that drive GC B-cell development and are relevant for human B-cell lymphomagenesis. Lippincott Williams & Wilkins 2021-06-01 /pmc/articles/PMC8171379/ /pubmed/34095765 http://dx.doi.org/10.1097/HS9.0000000000000582 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Hematology Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Review Basso, Katia Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title | Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title_full | Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title_fullStr | Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title_full_unstemmed | Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title_short | Biology of Germinal Center B Cells Relating to Lymphomagenesis |
title_sort | biology of germinal center b cells relating to lymphomagenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8171379/ https://www.ncbi.nlm.nih.gov/pubmed/34095765 http://dx.doi.org/10.1097/HS9.0000000000000582 |
work_keys_str_mv | AT bassokatia biologyofgerminalcenterbcellsrelatingtolymphomagenesis |