Abstract

Almost 30% of children in Southern Africa are HIV exposed but uninfected (HEU) and experience exposures that could increase vulnerability to infectious diseases compared to HIV unexposed (HU) children. The mechanisms of HEU infant vulnerability remain ill-defined. This review seeks to appraise the existing clinical evidence of the pattern of HEU infant infectious morbidity to aid understanding of the potential mechanism of susceptibility. A systematic search was conducted of scientific literature databases and conference proceedings up to December 2015 for studies comparing adequately defined HEU (in whom HIV-infection had been excluded through age-appropriate testing) and HU infants for all-cause mortality, all-cause hospitalization, or an infection-related morbidity. The systematic review was complemented by a narrative review of additional studies detailing the pattern of infectious morbidity experienced by HEU children without comparison to HU children or without conclusive exclusion of HIV-infection in HIV-exposed infants. Only 3 of 22 eligible identified studies were designed to primarily compare HEU and HU infants for infectious morbidity. Fourteen were conducted prior to 2009 in the context of limited antiretroviral interventions. Three patterns emerge: (1) causes of morbidity and mortality in HEU infants are consistent with the common causes of childhood morbidity and mortality (pneumonia, diarrheal disease, and bacterial sepsis) but occur with greater severity in HEU infants resulting in higher mortality, more frequent hospitalization, and more severe manifestations of disease; (2) the greatest relative difference between HEU and HU infants in morbidity and mortality occurs beyond the neonatal period, during mid-infancy, having waned by the second year of life; and (3) HEU infants are at greater risk than HU infants for invasive streptococcal infections specifically Group B Streptococcus and Streptococcus pneumonia. To definitively understand HEU infant infectious morbidity risk, substantially larger prospective studies with appropriate HU infant comparison groups are necessary. HEU children would benefit from collaboration among researchers to achieve the quality of evidence required to improve HEU infant outcomes globally. HEU infant health and well-being, beyond avoiding HIV-infection, deserves a more prominent position in the local and international HIV research agendas.

Highlights

  • Approximately 1.4 million HIV-infected women become pregnant annually (1)

  • The study demonstrated an almost four times greater risk of mortality [incidence rate ratio (IRR) 3.9, 95% CI 3.2–4.8] at 12 months and two times greater risk of mortality (IRR 2.0, 95% CI 1.2–3.5) at 24 months in HIV-exposed but uninfected (HEU) compared to HIV unexposed (HU) infants (33)

  • The IRR for all hospitalizations was 3.2, but the difference between HEU and HU infants was in non-malignant hematological disease and other non-specific symptoms (IRR 3.2, 95% CI 1.5–7.0) rather than infectious disease hospitalizations (IRR 1.0, 95% CI 0.79–1.37)

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Summary

Introduction

Approximately 1.4 million HIV-infected women become pregnant annually (1). Expanding vertical HIV transmission prevention (VTP) programs have markedly reduced HIV transmission, but for those HIV-exposed but uninfected (HEU) children, there are consequences of being born to an HIV-infected mother (1). Risk factors for HEU infant infectious morbidity and mortality can be divided into two groups: (1) Universal infant risk factors These include prematurity or small for gestational age, absence of or suboptimal breastfeeding, maternal mortality, exposure to infectious agents tuberculosis (TB), and poverty (2–11); (2) risk factors unique to HIV-exposed infants. These include exposure to the in utero environment altered by HIV, including exposure to viral proteins and glycoproteins, a pro-inflammatory state in the mother, maternal immune compromise, exposure to antiretroviral (ARV) and other drugs in utero and in breast milk (12–18). This review seeks to appraise the existing clinical evidence of the pattern of HEU infant infectious morbidity to aid understanding of the potential mechanism of susceptibility

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