The Interaction of Borrelia burgdorferi with Human Dendritic Cells: Functional Implications
- PMID: 37405694
- PMCID: PMC10527078
- DOI: 10.4049/jimmunol.2300235
The Interaction of Borrelia burgdorferi with Human Dendritic Cells: Functional Implications
Abstract
Dendritic cells bridge the innate and adaptive immune responses by serving as sensors of infection and as the primary APCs responsible for the initiation of the T cell response against invading pathogens. The naive T cell activation requires the following three key signals to be delivered from dendritic cells: engagement of the TCR by peptide Ags bound to MHC molecules (signal 1), engagement of costimulatory molecules on both cell types (signal 2), and expression of polarizing cytokines (signal 3). Initial interactions between Borrelia burgdorferi, the causative agent of Lyme disease, and dendritic cells remain largely unexplored. To address this gap in knowledge, we cultured live B. burgdorferi with monocyte-derived dendritic cells (mo-DCs) from healthy donors to examine the bacterial immunopeptidome associated with HLA-DR. In parallel, we examined changes in the expression of key costimulatory and regulatory molecules as well as profiled the cytokines released by dendritic cells when exposed to live spirochetes. RNA-sequencing studies on B. burgdorferi-pulsed dendritic cells show a unique gene expression signature associated with B. burgdorferi stimulation that differs from stimulation with lipoteichoic acid, a TLR2 agonist. These studies revealed that exposure of mo-DCs to live B. burgdorferi drives the expression of both pro- and anti-inflammatory cytokines as well as immunoregulatory molecules (e.g., PD-L1, IDO1, Tim3). Collectively, these studies indicate that the interaction of live B. burgdorferi with mo-DCs promotes a unique mature DC phenotype that likely impacts the nature of the adaptive T cell response generated in human Lyme disease.
Copyright © 2023 by The American Association of Immunologists, Inc.
Conflict of interest statement
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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References
-
- Steere AC, and Glickstein L. 2004. Elucidation of Lyme arthritis. Nature reviews 4: 143–152. - PubMed
-
- Aucott JN, Yang T, Yoon I, Powell D, Geller SA, and Rebman AW. 2022. Risk of post-treatment Lyme disease in patients with ideally-treated early Lyme disease: A prospective cohort study. International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 116: 230–237. - PubMed
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