The importance of B cell receptor isotypes and stereotypes in chronic lymphocytic leukemia.


Journal

Leukemia
ISSN: 1476-5551
Titre abrégé: Leukemia
Pays: England
ID NLM: 8704895

Informations de publication

Date de publication:
02 2019
Historique:
received: 05 07 2018
accepted: 08 10 2018
revised: 29 08 2018
pubmed: 18 12 2018
medline: 21 5 2019
entrez: 18 12 2018
Statut: ppublish

Résumé

B cell receptor (BCR) signaling is a central pathway promoting the survival and proliferation of normal and malignant B cells. Chronic lymphocytic leukemia (CLL) arises from mature B cells, expressing functional BCRs, mainly of immunoglobulin M (IgM) and IgD isotypes. Importantly, 30% of CLL patients express quasi-identical BCRs, the so-called "stereotyped" receptors, indicating the existence of common antigenic determinants, which may drive disease initiation and favor its progression. Although the antigenic specificity of IgM and IgD receptors is identical, there are distinct isotype-specific responses after IgM and IgD triggering. Here, we discuss the most important steps of normal B cell development, and highlight the importance of BCR signaling for CLL pathogenesis, with a focus on differences between IgM and IgD isotype signaling. We also highlight the main characteristics of CLL patient subsets, based on BCR stereotypy, and describe subset-specific BCR function and antigen-binding characteristics. Finally, we outline the key biologic and clinical responses to kinase inhibitor therapy, targeting the BCR-associated Bruton's tyrosine kinase, phosphoinositide-3-kinase, and spleen tyrosine kinase in patients with CLL.

Identifiants

pubmed: 30555163
doi: 10.1038/s41375-018-0303-x
pii: 10.1038/s41375-018-0303-x
pmc: PMC7182338
mid: NIHMS1575737
doi:

Substances chimiques

Immunoglobulin Isotypes 0
Receptors, Antigen, B-Cell 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

287-298

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research)
ID : 9965
Pays : International
Organisme : UT | University of Texas MD Anderson Cancer Center (MD Anderson)
ID : CA016672
Pays : International

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Auteurs

Elisa Ten Hacken (E)

Department of Leukemia, Unit 428, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Medical Oncology, Dana Farber Cancer Institute, Boston, MA, USA.

Maria Gounari (M)

Institute of Applied Biosciences, Centre for Research and Technology Hellas, Thessaloniki, Greece.

Paolo Ghia (P)

Strategic Research Program on CLL, IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milan, Italy.

Jan A Burger (JA)

Department of Leukemia, Unit 428, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. jaburger@mdanderson.org.

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