Abstract

Microbial translocation (MT) markers are indicators of HIV-related immune activation, but reference values are mostly derived from European or North American populations and could be substantially different in populations living in developing countries. Here we evaluate possible differences in MT markers levels in HIV+ pregnant women of different geographical provenance. This study is nested within an observational study of pregnant women with HIV in Italy. Women were dichotomized on the basis of provenance in two groups of European (n = 14) and African (n = 26) origin. Soluble CD14, lipopolysaccharide-binding protein (LBP) and intestinal-fatty acid binding protein (I-FABP) were measured in plasma samples collected between the first and second trimester of pregnancy. Demographic and viroimmunological characteristics were similar between groups, although European women were more commonly smokers and HCV-coinfected. Irrespective of origin, LBP plasma levels were positively correlated with I-FABP (r = 0.467, p = 0.004) and sCD14 levels (r = 0.312 p = 0.060). Significantly higher levels of sCD14 (1885 vs. 1208 ng/mL, p = 0.005) LBP (28.5 vs. 25.3 µg/mL, p = 0.050) and I-FABP (573.4 vs. 358.2 pg/mL, p = 0.002) were observed in European compared with African women. A multivariable linear regression analysis, adjusted for smoking and HCV coinfection confirmed the association between sCD14 levels and women provenance (p = 0.03). Our observations indicate significant differences in soluble markers among women of different provenance. In the design and analysis of studies evaluating MT markers, population-specific reference values should be considered.

Highlights

  • Microbial translocation (MT) markers are indicators of HIV-related immune activation, but reference values are mostly derived from European or North American populations and could be substantially different in populations living in developing countries

  • Circulating level of lipopolysaccharides (LPS) have been identified as a valuable indicator of immune inflammation [1,3], but since the measurement of LPS concentration in plasma is a technically complex task, other reliable biomarkers of microbial translocation have been identified and validated: elevated plasma levels of LPS binding protein (LBP), index of LPS exposure, intestinal fatty acid-binding protein (IFABP), marker of enterocytes damage, and soluble CD14, that correctly reflects the degree of LPS-induced inflammation in HIV+ individuals [4]

  • We report that HIV pregnant women of African origin had lower MT markers levels when compared with European women of similar age, weight and gestational age at time of sampling

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Summary

Introduction

Microbial translocation (MT) markers are indicators of HIV-related immune activation, but reference values are mostly derived from European or North American populations and could be substantially different in populations living in developing countries. HIV replicates vigorously in gut-associated lymphoid tissue (GALT), causing damage to the intestinal barrier through several mechanisms, and allows systemic dissemination of microbial products, resulting in secretion of inflammatory mediators. Circulating level of lipopolysaccharides (LPS) have been identified as a valuable indicator of immune inflammation [1,3], but since the measurement of LPS concentration in plasma is a technically complex task, other reliable biomarkers of microbial translocation have been identified and validated: elevated plasma levels of LPS binding protein (LBP), index of LPS exposure, intestinal fatty acid-binding protein (IFABP), marker of enterocytes damage, and soluble CD14 (sCD14), that correctly reflects the degree of LPS-induced inflammation in HIV+ individuals [4].

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