AI Article Synopsis

  • This study examines how sex-based differences in immune cell composition and function affect adaptive immune responses in human lymphoid tissues, specifically tonsils.
  • It found that female tonsils had more memory B cells and produced stronger antibody responses to influenza, particularly after live-attenuated vaccination, compared to male tonsils.
  • Additionally, differences in CD4 T cell profiles were seen in adults, indicating that these variations may help explain why males and females respond differently to vaccines and viral infections.

Article Abstract

Sex-based differences in immune cell composition and function can contribute to distinct adaptive immune responses. Prior work has quantified these differences in peripheral blood, but little is known about sex differences within human lymphoid tissues. Here, we characterized the composition and phenotypes of adaptive immune cells from male and female ex vivo tonsils and evaluated their responses to influenza antigens using an immune organoid approach. In a pediatric cohort, female tonsils had more memory B cells compared to male tonsils direct ex vivo and after stimulation with live-attenuated but not inactivated vaccine, produced higher influenza-specific antibody responses. Sex biases were also observed in adult tonsils but were different from those measured in children. Analysis of peripheral blood immune cells from vaccinated adults also showed higher frequencies of tissue homing CD4 T cells in female participants. Together, our data demonstrate that distinct memory B and T cell profiles are present in male vs. female lymphoid tissues and peripheral blood respectively and suggest that these differences may in part explain sex biases in response to vaccines and viruses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11133680PMC
http://dx.doi.org/10.3389/fimmu.2024.1373537DOI Listing

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