B cells and cancer: To B or not to B?

Author:

Fridman Wolf Herman1ORCID,Petitprez Florent2ORCID,Meylan Maxime1ORCID,Chen Tom Wei-Wu3ORCID,Sun Cheng-Ming1ORCID,Roumenina Lubka T.1ORCID,Sautès-Fridman Catherine1ORCID

Affiliation:

1. Centre de Recherche des Cordeliers, Sorbonne Université, Institut national de la santé et de la recherche médicale, Université de Paris, Paris, France

2. Programme Cartes d’Identité des Tumeurs, Ligue Nationale contre le Cancer, Paris, France

3. Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan

Abstract

Whereas T cells have been considered the major immune cells of the tumor microenvironment able to induce tumor regression and control cancer clinical outcome, a burst of recent publications pointed to the fact that B cells may also play a prominent role. Activated in germinal centers of tertiary lymphoid structures, B cells can directly present tumor-associated antigens to T cells or produce antibodies that increase antigen presentation to T cells or kill tumor cells, resulting in a beneficial clinical impact. Immune complexes can also increase inflammation, angiogenesis, and immunosuppression via macrophage and complement activation, resulting in deleterious impact.

Funder

Institut national de la santé et de la recherche médicale

Sorbonne Université, Université de Paris

Site Intégré de Recherche sur le Cancer

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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