Lung B cells in ectopic germinal centers undergo affinity maturation

S Stephane M. Guillaume (Immunology Program, Babraham Institute) W William S. Foster (Immunology Program, Babraham Institute) I Isabel San Martín Molina (Immunology Program, Babraham Institute) E Emily M. Watson (Immunology Program, Babraham Institute) S Silvia Innocentin (Immunology Program, Babraham Institute) G Grant M. Kennedy (Immunology Program, Babraham Institute) A Alice E. Denton (Department of Immunology and Inflammation, Imperial College London) M Michelle A. Linterman (Immunology Program, Babraham Institute)

Abstract

The lungs are constantly exposed to the external environment and a myriad of antigenic challenges within the air. Chronic exposure to allergens and other airborne antigens can result in the formation of lymphocyte aggregates in the lung, which can harbor ectopic germinal centers (GCs). After allergen exposure, GCs that form in the lung are much smaller and less densely packed with B cells than lymph node GCs. Despite this, ectopic lung GCs support somatic hypermutation and affinity-based maturation as in lymph node GCs, and export memory B cells (MBCs) directly into the lung tissue. This demonstrates that the lung can locally diversify B cell responses and supports the generation of tissue MBC populations in situ.

Article Details

Volume / Issue Vol. 122, Issue 14
Published April 08, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

S

Stephane M. Guillaume

Immunology Program, Babraham Institute

W

William S. Foster

Immunology Program, Babraham Institute

I

Isabel San Martín Molina

Immunology Program, Babraham Institute

E

Emily M. Watson

Immunology Program, Babraham Institute

S

Silvia Innocentin

Immunology Program, Babraham Institute

G

Grant M. Kennedy

Immunology Program, Babraham Institute

A

Alice E. Denton

Department of Immunology and Inflammation, Imperial College London

M

Michelle A. Linterman

Immunology Program, Babraham Institute