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Elevated CD153 Expression on Aged T Follicular Helper Cells is Vital for B cell Responses. | LitMetric

AI Article Synopsis

  • - Recent research indicates that an abnormal population of T follicular helper cells (Tfh10) that produces IL-10 accumulates with age, contributing to reduced effectiveness of vaccines in older adults.
  • - Analysis revealed that aged Tfh and Tfh10 cells show increased CD153 expression, linked to higher IL-6 levels and the molecule c-Maf, which are associated with "inflammaging."
  • - Blocking CD153 in older mice led to decreased vaccine-driven antibody responses, highlighting that while Tfh cell function declines with age, increased CD153 may still enhance some of their activity in response to vaccines.

Article Abstract

Our recent data showed that an aberrant IL-10-producing T follicular helper population (Tfh10) accumulates dramatically with age and is associated with age-related declines in vaccine responsiveness. Through single cell gene expression and chromatin accessibility analysis of IL-10 and IL-10 memory CD4+ T cells from young and aged mice, we identified increased expression of CD153 on aged Tfh and Tfh10 cells. Mechanistically, we linked inflammaging (increased IL-6 levels) to elevated CD153 expression of Tfh cells through c-Maf. Surprisingly, blockade of CD153 in aged mice significantly reduced their vaccine-driven antibody response, which was associated with decreased expression of ICOS on antigen-specific Tfh cells. Combined, these data show that an IL-6/c-Maf/CD153 circuit is critical for maintaining ICOS expression. Thus, although overall Tfh-mediated B cell responses are reduced in the context of vaccines and aging, our data suggest that elevated expression of CD153 on Tfh cells potentiates the remaining Tfh function in aged mice.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055293PMC
http://dx.doi.org/10.1101/2023.03.17.533214DOI Listing

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