Early regional lymph node activation drives influenza vaccine responses in an ancestrally diverse cohort
Jacqueline H. Y. SiuiD, Sofia CoelhoiD, Aime PalomerasiD, Sandra Belij‐RammerstorferiD, Ninisha BarmaniD, Chloe Hyun-Jung LeeiD, Tamara Ströbel, Christopher J. ThorpeiD, Charandeep Kaur, Tom Cole, Nico RemmertiD, Jamie FowleriD, Sam Pledger, Kyla DooleyiD, Terrence ChaniD, Katja HöschleriD, Maria Zambon, Daniel Opoka, Tamás SzommeriD, Seung J. Kim, Vinod Kumar, Samantha VanderslottiD, Pontiano KaleebuiD, Anita MiliciciD, Donald B. Palmer, , Katrina M. PollockiD
Abstract
Early in vivo dynamics of human immune-cell activation across regionally activated lymphoid tissue sites upon immunisation are poorly characterised in ancestrally diverse individuals. Here, we profiled draining and non-draining axillary lymph nodes (dLNs and ndLNs) by ultrasound-guided fine-needle aspiration (FNA) in 13 Black and Asian ancestry individuals, before and 3-7 days after vaccination with adjuvanted influenza vaccine. Draining but not ndLNs rapidly increased in size post-vaccination, by day 3, with distinct cellular dynamics determined through single cell multiomics. Dissecting LN cellular diversity into 42 lymphoid and non-lymphoid cell states, post-vaccination cell abundance changes were observed across all LNs, but dLNs were specifically characterised by CD4+ T follicular helper (CD4+ Tfh) cell expansion. Gene expression analysis revealed a dLN post-vaccination hub of multicellular activity defined by CD4+ Tfh signalling, cross-compartmental activation, translation, and enhanced antigen-presentation capacity. Thus, robust responses to intramuscular immunisation transcending ancestral inter-individual variation are elicited through temporal, anatomical and cellular lymphatic co-ordination with implications for vaccine design in ancestrally diverse populations. SummaryIn this study of ancestrally diverse young adults, the temporarily co-ordinated response to an adjuvanted influenza vaccine at lymph nodes local to (draining) and distal from (non-draining) the injection site, reveals early regulation of cellular kinetics and anatomical hierarchy of the innate and adaptive immune responses.
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