4.6 Review

Immunology of pediatric HIV infection

Journal

IMMUNOLOGICAL REVIEWS
Volume 254, Issue -, Pages 143-169

Publisher

WILEY
DOI: 10.1111/imr.12074

Keywords

HIV; children; neonatal; gut microbiota; breast milk; Th17; regulatory T-cells

Categories

Funding

  1. National Institute of Health [R01 HD 39611, R01 HD 40777, R01 HD 57617, AI 100147]
  2. International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT)
  3. National Institute of Allergy and Infectious Diseases (NIAID) [U01 AI 68632]
  4. Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  5. National Institute of Mental Health (NIMH) [AI 68632]

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Most infants born to human immunodeficiency virus (HIV)-infected women escape HIV infection. Infants evade infection despite an immature immune system and, in the case of breastfeeding, prolonged repetitive exposure. If infants become infected, the course of their infection and response to treatment differs dramatically depending upon the timing (in utero, intrapartum, or during breastfeeding) and potentially the route of their infection. Perinatally acquired HIV infection occurs during a critical window of immune development. HIV's perturbation of this dynamic process may account for the striking age-dependent differences in HIV disease progression. HIV infection also profoundly disrupts the maternal immune system upon which infants rely for protection and immune instruction. Therefore, it is not surprising that infants who escape HIV infection still suffer adverse effects. In this review, we highlight the unique aspects of pediatric HIV transmission and pathogenesis with a focus on mechanisms by which HIV infection during immune ontogeny may allow discovery of key elements for protection and control from HIV.

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