Serum anti-flagellin and anti-lipopolysaccharide immunoglobulins as predictors of linear growth faltering in Pakistani infants at risk for environmental enteric dysfunction

PLoS One. 2018 Mar 6;13(3):e0193768. doi: 10.1371/journal.pone.0193768. eCollection 2018.

Abstract

Background: Environmental Enteric Dysfunction (EED) in children from low-income countries has been linked to linear growth declines. There is a critical need to identify sensitive and early EED biomarkers.

Objective: Determine whether levels of antibodies against bacterial components flagellin (flic) and lipopolysaccharide (LPS) predict poor growth.

Design/methods: In a prospective birth cohort of 380 children in rural Pakistan blood and stool samples were obtained at ages 6 and 9 months. Linear mixed effects models were used to examine longitudinal associations between quartiles of anti-flic and anti-LPS antibodies and changes in LAZ, WAZ and WLZ scores. Spearman's correlations were measured between anti-flic and anti-LPS immunoglobulins with measures of systemic/enteric inflammation and intestinal regeneration.

Results: Anti-LPS IgA correlated significantly with CRP, AGP and Reg1 serum at 6mo and with MPO at 9mo. In multivariate analysis at 6mo of age, higher anti-LPS IgA levels predicted greater declines in LAZ scores over subsequent 18mo (comparing highest to lowest quartile, β (SE) change in LAZ score/year = -0.313 (0.125), p-value = 0.013). Anti-flic Ig A in the two highest quartiles measured at 9mo of age had declines in LAZ of -0.269 (0.126), p = 0.033; and -0.306 (0.129), p = 0.018 respectively, during the subsequent 18mo of life, compared to those in the lowest quartile of anti-flic IgA.

Conclusions and relevance: Elevated anti-flic IgA and anti-LPS IgA antibodies at 6 and 9mo, predict declines in linear growth. Systemic and enteric inflammation correlated with anti-LPS IgA provides mechanistic considerations for potential future interventions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asymptomatic Infections
  • Biomarkers / blood
  • Child Development*
  • Feces / microbiology
  • Female
  • Flagellin / immunology*
  • Follow-Up Studies
  • Humans
  • Immunoglobulin A / blood*
  • Infant
  • Infections / complications
  • Intestinal Diseases / epidemiology
  • Intestinal Diseases / immunology*
  • Intestinal Diseases / microbiology
  • Linear Models
  • Lipopolysaccharides / immunology*
  • Longitudinal Studies
  • Male
  • Malnutrition / complications
  • Multivariate Analysis
  • Pakistan
  • Prospective Studies
  • Risk
  • Rural Population

Substances

  • Biomarkers
  • Immunoglobulin A
  • Lipopolysaccharides
  • Flagellin