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Clinical and immunological outcomes of HIV-exposed uninfected and HIV-unexposed uninfected children in the first 24 months of life in Western Kenya.
Ray, Jessica E; Dobbs, Katherine R; Ogolla, Sidney O; Daud, Ibrahim I; Midem, David; Omenda, Maxwel M; Nowacki, Amy S; Beeson, James G; Sabourin, Katherine R; Rochford, Rosemary; Dent, Arlene E.
  • Ray JE; Center for Global Health & Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA.
  • Dobbs KR; Center for Global Health & Diseases, Case Western Reserve University, 10900 Euclid Avenue LC: 4983, Cleveland, OH, 44106, USA. kxd179@case.edu.
  • Ogolla SO; Division of Pediatric Infectious Diseases, University Hospitals Rainbow Babies and Children's Hospital, LC: 4983, Cleveland, OH, 44106, USA. kxd179@case.edu.
  • Daud II; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Midem D; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Omenda MM; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Nowacki AS; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Beeson JG; Department of Quantitative Health Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA.
  • Sabourin KR; Burnet Institute, Melbourne, VIC, Australia.
  • Rochford R; Department of Immunology and Microbiology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
  • Dent AE; Department of Immunology and Microbiology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
BMC Infect Dis ; 24(1): 156, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38302888
ABSTRACT

BACKGROUND:

Previous studies show increased morbidity in children who are HIV-exposed but uninfected (HEU) compared to children who are HIV-unexposed uninfected (HUU). We sought to evaluate the effects of prenatal HIV exposure on clinical and immunological outcomes in the first 24 months of life.

METHODS:

Eighty-five HEU and 168 HUU children from Kenya were followed from birth to 24 months. All mothers living with HIV received combination antiretroviral therapy. Children who were HEU received standard-of-care cotrimoxazole prophylaxis through 18 months. Episodes of acute illness were identified through a combination of active and passive follow up. Trajectories of plasma cytokines, vaccine-specific antibodies, and antimalarial antibodies were examined.

RESULTS:

Children who were HEU and children who were HUU had similar growth curves. Children who were HEU had lower rates of malaria (rate ratio 0.54, 95% CI 0.38, 0.77) and respiratory illness (rate ratio 0.80, 95% CI 0.68, 0.93). Trajectories of plasma cytokines and vaccine-specific antibodies were similar in children who were HEU and HUU. There were subtle differences in antimalarial antibody dynamics, in which children who were HEU had overall lower antibody levels against five of the 14 malaria antigens tested.

CONCLUSIONS:

Children who were HEU and born to optimally treated mothers living with HIV had similar growth characteristics and immune profiles compared to children who were HUU. Children who were HEU had reduced risk for malaria and respiratory illness, which may be secondary to cotrimoxazole prophylaxis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacunas / Infecciones por VIH / Malaria / Antimaláricos Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Infant / Pregnancy País como asunto: Africa Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacunas / Infecciones por VIH / Malaria / Antimaláricos Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Infant / Pregnancy País como asunto: Africa Idioma: En Año: 2024 Tipo del documento: Article