Author:
Mitul Mahina Tabassum,Kastenschmidt Jenna M.,Sureshchandra Suhas,Wagoner Zachary W.,Sorn Andrew M.,Mcllwain David R.,Hernandez-Davies Jenny E.,Jain Aarti,de Assis Rafael,Trask Douglas,Davies D. Huw,Wagar Lisa E.
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 in vivo 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.
Funder
Bill and Melinda Gates Foundation
National Institute of Allergy and Infectious Diseases