The Wonder Years: What Can Primary School Children Teach Us About Immunity to <i>Mycobacterium tuberculosis</i>?
Seddon JA, Chiang SS, Esmail H, Coussens AK
Frontiers in immunology · 2018-12
Abstract
In high burden settings, the risk of infection with Mycobacterium tuberculosis increases throughout childhood due to cumulative exposure. However, the risk of progressing from tuberculosis (TB) infection to disease varies by age. Young children ( M. tuberculosis is central to these issues. Host response at key stages in the immunopathological interaction with M. tuberculosis influences risk and disease phenotype. Cell numbers and function change dramatically with age and sexual maturation. Young children have poorly functioning innate cells and a Th2 skew. During the "Wonder Years," there is a lymphocyte predominance and a Th1 skew. During puberty, neutrophils become more central to host response, and CD4+ T cells increase in number. Sex hormones (dehydroepiandrosterone, adiponectin, leptin, oestradiol, progesterone, and testosterone) profoundly affect immunity. Compared to girls, boys have a stronger Th1 profile and increased numbers of CD8+ T cells and NK cells. Girls are more Th2-skewed and elicit more enhanced inflammatory responses. Non-immunological factors (including exposure intensity, behavior, and co-infections) may impact disease. However, given the consistent patterns seen across time and geography, these factors likely are less central. Strategies to protect children and adolescents from TB may need to differ by age and sex. Further work is required to better understand the contribution of age and sex to M. tuberculosis immunity.
MeSH terms
- Humans
- Mycobacterium tuberculosis
- Tuberculosis
- Disease Progression
- Tuberculosis Vaccines
- Incidence
- Age Factors
- Sex Factors
- Sexual Maturation
- Adolescent
- Adult
- Child
- Host-Pathogen Interactions
- Immunity, Innate
- Young Adult