B cell heterogeneity in human tuberculosis highlights compartment-specific phenotype and functional roles.
Robert KrausePaul OgongoLiku TezeraMohammed AhmedIan MbanoMark ChambersAbigail NgoepeMagalli MagnoumbaDaniel MuemaFarina KarimKhadija KhanKapongo LumambaKievershen NarganRajhmun MadanseinAdrie J C SteynAlex K ShalekPaul ElkingtonAlasdair LesliePublished in: Communications biology (2024)
B cells are important in tuberculosis (TB) immunity, but their role in the human lung is understudied. Here, we characterize B cells from lung tissue and matched blood of patients with TB and found they are decreased in the blood and increased in the lungs, consistent with recruitment to infected tissue, where they are located in granuloma associated lymphoid tissue. Flow cytometry and transcriptomics identify multiple B cell populations in the lung, including those associated with tissue resident memory, germinal centers, antibody secretion, proinflammatory atypical B cells, and regulatory B cells, some of which are expanded in TB disease. Additionally, TB lungs contain high levels of Mtb-reactive antibodies, specifically IgM, which promotes Mtb phagocytosis. Overall, these data reveal the presence of functionally diverse B cell subsets in the lungs of patients with TB and suggest several potential localized roles that may represent a target for interventions to promote immunity or mitigate immunopathology.
Keyphrases
- mycobacterium tuberculosis
- pulmonary tuberculosis
- flow cytometry
- single cell
- endothelial cells
- gene expression
- physical activity
- transcription factor
- working memory
- machine learning
- patient safety
- human immunodeficiency virus
- deep learning
- hepatitis c virus
- hiv infected
- antiretroviral therapy
- pluripotent stem cells