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- W4296798813 abstract "With age, senescence-associated (SA) CD4+ T cells that are refractory to T cell receptor (TCR) stimulation are increased along with spontaneous germinal center (Spt-GC) development prone to autoantibody production. We demonstrate that CD153 and its receptor CD30 are expressed in SA-T and Spt-GC B cells, respectively, and deficiency of either CD153 or CD30 results in the compromised increase of both cell types. CD153 engagement on SA-T cells upon TCR stimulation causes association of CD153 with the TCR/CD3 complex and restores TCR signaling, whereas CD30 engagement on GC B cells induces their expansion. Administration of an anti-CD153 antibody blocking the interaction with CD30 suppresses the increase in both SA-T and Spt-GC B cells with age and ameliorates lupus in lupus-prone mice. These results suggest that the molecular interaction of CD153 and CD30 plays a central role in the reciprocal activation of SA-T and Spt-GC B cells, leading to immunosenescent phenotypes and autoimmunity." @default.
- W4296798813 created "2022-09-24" @default.
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- W4296798813 date "2022-09-01" @default.
- W4296798813 modified "2023-10-13" @default.
- W4296798813 title "cis interaction of CD153 with TCR/CD3 is crucial for the pathogenic activation of senescence-associated T cells" @default.
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- W4296798813 doi "https://doi.org/10.1016/j.celrep.2022.111373" @default.
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