Pattern recognition receptor-mediated cytokine response in infants across 4 continents

J Allergy Clin Immunol. 2014 Mar;133(3):818-26.e4. doi: 10.1016/j.jaci.2013.09.038. Epub 2013 Nov 28.

Abstract

Background: Susceptibility to infection as well as response to vaccination varies among populations. To date, the underlying mechanisms responsible for these clinical observations have not been fully delineated. Because innate immunity instructs adaptive immunity, we hypothesized that differences between populations in innate immune responses may represent a mechanistic link to variation in susceptibility to infection or response to vaccination.

Objective: Determine whether differences in innate immune responses exist among infants from different continents of the world.

Methods: We determined the innate cytokine response following pattern recognition receptor (PRR) stimulation of whole blood from 2-year-old infants across 4 continents (Africa, North America, South America, and Europe).

Results: We found that despite the many possible genetic and environmental exposure differences in infants across 4 continents, innate cytokine responses were similar for infants from North America, South America, and Europe. However, cells from South African infants secreted significantly lower levels of cytokines than did cells from infants from the 3 other sites, and did so following stimulation of extracellular and endosomal but not cytosolic PRRs.

Conclusions: Substantial differences in innate cytokine responses to PRR stimulation exist among different populations of infants that could not have been predicted. Delineating the underlying mechanism(s) for these differences will not only aid in improving vaccine-mediated protection but possibly also provide clues for the susceptibility to infection in different regions of the world.

Keywords: Innate immunity; global; immune development; infectious disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child, Preschool
  • Cytokines / biosynthesis*
  • Disease Susceptibility
  • Humans
  • Immunity, Innate
  • Infant
  • Infant Mortality
  • Infections / immunology
  • Infections / mortality
  • Receptors, Pattern Recognition / physiology*
  • Toll-Like Receptors / physiology

Substances

  • Cytokines
  • Receptors, Pattern Recognition
  • Toll-Like Receptors