HIBA: Healthy Immune & Brain Adolescence

  • Research type

    Research Study

  • Full title

    Adolescent development of the immune system and its relationship to normal changes in brain and behavior: a two-stage study

  • IRAS ID

    155446

  • Contact name

    Edward T. Bullmore

  • Contact email

    etb23@cam.ac.uk

  • Sponsor organisation

    Cambridgeshire and Peterborough NHS Foundation Trust

  • Research summary

    Adolescence is a period of major changes in behaviour and brain organization, and of increased risk for the development of psychiatric disorder. There are major developmental changes in immune structure and function during this period. We hypothesize that behavioural and brain changes are linked to developmental processes in the immune system. We propose to reproduce and extend what is already known about developmental changes in the peripheral immunophenotype of normal adolescents and young adults. We expect to reproduce prior data demonstrating reductions in thymic output of naïve CD4+ and CD8+ T cells, using a peripheral marker of thymic involution, over the course of adolescence. We will test the prediction that thymically generated naïve T cells or recent thymic emigrants (measured by TRECs [T cell receptor excision circles]) are reduced in peripheral venous blood samples from a cohort of normal young adults (N=10; aged 22-24) compared to a younger cohort (N=10, aged 14-15 inclusive). We will explore cellular, transcriptomic and genetic markers using multivariate statistics and network analysis to identify changes in peripheral immunophenotypes linked to the TREC signature of thymic involution. We will measure thymic involution directly by magnetic resonance spectroscopy (i.e., MRI scan). If the results of this first study confirm that we can measure developmental processes in the peripheral immune system over the course of adolescence, we will proceed to collect comparable additional cohort data (N=80) to map developmental processes more continuously as a function of age and/or to test the hypothesis of normal gender dimorphism in immune system development. We will recruit participants from the pre-existing NSPN cohort and U-Change cohort.

  • REC name

    East of England - Cambridge South Research Ethics Committee

  • REC reference

    14/EE/1058

  • Date of REC Opinion

    15 Aug 2014

  • REC opinion

    Further Information Favourable Opinion