# B cells and iBALT in TB immunity & pathogenesis

## TL;DR

This paper reviews how B cells and iBALT contribute to tuberculosis immunity, highlighting their role in immune responses and potential for vaccine development.

## Contribution

The paper synthesizes evidence on B cells and iBALT in TB, emphasizing their underappreciated roles and sex-based differences.

## Key findings

- B cells contribute to iBALT formation, which enhances localized immune responses in TB.
- Sex differences in iBALT formation may influence TB immunity and disease outcomes.
- B cells and iBALT have potential implications for TB vaccine development and immunotherapy.

## Abstract

B cells play a crucial role in immunity against various infectious diseases. However, their role in tuberculosis (TB) has been largely understudied. Emerging evidence suggests that B cells actively shape immune responses in TB. Beyond their classical functions, B cells contribute to the formation of inducible bronchus-associated lymphoid tissue (iBALT), a tertiary lymphoid structure (TLS) that enhances localized immune responses in the lungs. As iBALT is a site for B-T cell interactions and the generation of high-affinity antibodies, recent studies suggest that sex differences in iBALT formation influence TB immunity. This review synthesizes evidence from both TB and non-TB models to highlight the expanding role of B cells and iBALT, underscoring their potential implications for vaccine development and immunotherapy.