PT - JOURNAL ARTICLE AU - Marcin L Pekalski AU - Arcadio Rubio García AU - Ricardo C Ferreira AU - Daniel B Rainbow AU - Deborah J Smyth AU - Meghavi Mashar AU - Jane Brady AU - Natalia Savinykh AU - Xaquin Castro Dopico AU - Sumiyya Mahmood AU - Simon Duley AU - Helen E Stevens AU - Neil M Walker AU - Antony J Cutler AU - Frank Waldron-Lynch AU - David B Dunger AU - Claire Shannon-Lowe AU - Alasdair J Coles AU - Joanne L Jones AU - Chris Wallace AU - John A Todd AU - Linda S Wicker TI - Recent thymic emigrants produce antimicrobial IL-8, express complement receptors and are precursors of a tissue-homing Th8 lineage of memory cells AID - 10.1101/059535 DP - 2016 Jan 01 TA - bioRxiv PG - 059535 4099 - http://biorxiv.org/content/early/2016/12/12/059535.short 4100 - http://biorxiv.org/content/early/2016/12/12/059535.full AB - The adaptive immune system utilizes multiple mechanisms linked to innate immune cell functions to respond appropriately to pathogens and commensals. Here we discover further aspects of this connectivity by demonstrating that naïve T cells as they emerge from the thymus (recent thymic emigrants, RTEs) express complement receptors (CR1 and CR2), the bacterial pathogen recognition receptor TLR1 and an enzyme that deactivates bacterial lipopolysaccharide (AOAH) and following activation secrete the anti-microbial cytokine IL-8. CR2+ naïve T cells also express a selection of genes associated with tissue migration, consistent with the hypothesis that following emigration from the thymus RTEs seed peripheral compartments where some pursue their anti-microbial potential by becoming IL-8-producing CR2+ memory cells while others undergo homeostatic expansion. CR2+ naïve and memory cells are abundant in children but decrease with age, coinciding with the involution of the thymus. The ability of CR2, which is also a receptor for Epstein-Barr Virus (EBV), to identify recent thymic emigrants will facilitate assessment of thymic function during aging and aid investigations of multiple clinical areas including the occurrence of T cell lymphomas caused by EBV.