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Objective : T cells are crucial in the pathogenesis of systemic lupus erythematosus (SLE) by secreting inflammatory cytokines, helping autoantibody production, and forming autoreactive memory T cell.
Objective T cells are crucial in the pathogenesis of systemic lupus erythematosus (SLE) by secreting inflammatory cytokines, helping autoantibody production, and forming autoreactive memory T cell.
Methods : The MRL/lpr mouse, a mouse model of NPSLE , was either systemically depleted of CD4+ T cells or intraventricularly injected with choroid plexus (CP) infiltrating T cells and subsequently assessed for changes in neuropsychiatric performan.
Methods The MRL/lpr mouse, a mouse model of NPSLE , was either systemically depleted of CD4+ T cells or intraventricularly injected with choroid plexus (CP) infiltrating T cells and subsequently assessed for changes in neuropsychiatric performan.
Results Systemic depletion of CD4+ T cells ameliorated systemic disease and cognitive defici.
Conclusions T cells, more specifically CP -infiltrating antigen-specific T cells, contribute to the pathogenesis of NPSLE , suggesting that modulating T cells may have therapeutic potential in the development of therapeutics targeting NPSL.
Moore,.
, Huang, MW, Reynolds, CA, Macian,.
and Putterman,.
(2022), Choroid plexus-infiltrating T cells drive murine neuropsychiatric lup.
Arthritis Rheumat.
Accepted Author Manuscri.
https://d.
org/11002/a.
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