Venous-plexus-associated lymphoid hubs support meningeal humoral immunity.
Zachary FitzpatrickNagela Ghabdan ZanluquiJared Spencer RosenblumZewen Kelvin TuongColin Y C LeeVikram ChandrashekharMaria Luciana Negro-DemontelAndrew P StewartDavid A PosnerMonica BuckleyKieren S J AllinsonPanagiotis MastorakosPrashant ChittaboinaDragan MaricDanielle R DonahueAdel E HelmyTamara TajsicJohn R FerdinandAnais PortetAna PeñalverEleanor GillmanZhengping ZhuangMenna R ClatworthyDorian B McGavernPublished in: Nature (2024)
There is increasing interest in how immune cells in the meninges-the membranes that surround the brain and spinal cord-contribute to homeostasis and disease in the central nervous system 1,2 . The outer layer of the meninges, the dura mater, has recently been described to contain both innate and adaptive immune cells, and functions as a site for B cell development 3-6 . Here we identify organized lymphoid structures that protect fenestrated vasculature in the dura mater. The most elaborate of these dural-associated lymphoid tissues (DALT) surrounded the rostral-rhinal confluence of the sinuses and included lymphatic vessels. We termed this structure, which interfaces with the skull bone marrow and a comparable venous plexus at the skull base, the rostral-rhinal venolymphatic hub. Immune aggregates were present in DALT during homeostasis and expanded with age or after challenge with systemic or nasal antigens. DALT contain germinal centre B cells and support the generation of somatically mutated, antibody-producing cells in response to a nasal pathogen challenge. Inhibition of lymphocyte entry into the rostral-rhinal hub at the time of nasal viral challenge abrogated the generation of germinal centre B cells and class-switched plasma cells, as did perturbation of B-T cell interactions. These data demonstrate a lymphoid structure around vasculature in the dura mater that can sample antigens and rapidly support humoral immune responses after local pathogen challenge.
Keyphrases
- immune response
- induced apoptosis
- spinal cord
- dendritic cells
- bone marrow
- cell cycle arrest
- toll like receptor
- chronic rhinosinusitis
- gene expression
- ultrasound guided
- mesenchymal stem cells
- oxidative stress
- sars cov
- endoplasmic reticulum stress
- high resolution
- spinal cord injury
- network analysis
- cell proliferation
- neuropathic pain
- multiple sclerosis
- pi k akt
- subarachnoid hemorrhage
- mass spectrometry
- wild type