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a Department of
Medical Microbiology, St George's Hospital Medical School, Cranmer
Terrace, London SW17 ORE, UK, b Paediatric Infectious Diseases Unit, St
George's Hospital Medical School, c Department of Ophthalmology, St George's
Hospital Medical School, d Department
of Paediatrics, St Thomas's Hospital, London SE1 7EH, UK
Correspondence to: Dr Boriskin.
Accepted 5 October
1998
OBJECTIVE
A one year
study of the relation between cytomegalovirus (CMV) and human
immunodeficiency virus (HIV) viral loads in a cohort of children with
vertically acquired HIV-1 infection.
DESIGN
Comparative
analysis of viral load measurements for CMV and HIV-1 in peripheral
blood leucocytes (PBLs) of individual children in relation to age and
clinical staging.
METHODS
Nested
polymerase chain reaction (PCR) was used to measure HIV-1 proviral DNA
and CMV genomic DNA in PBLs of 56 children.
RESULTS
The CMV load
was highest in 0-2 year old HIV positive children with stage C disease
(range, 1-7143 copies/100 ng DNA; median, 125) and was significantly
lower in older children. Although higher in young children, HIV-1 viral
load did not show the same marked reduction with age that is seen with
CMV. Over a one year period, testing of serial samples for both viruses
in a subgroup of children revealed a discordant relation between viral
loads for CMV and HIV-1.
CONCLUSIONS
CMV
viral load falls much faster than HIV viral load in dually infected
children. Screening for clinical CMV disease is most likely to be of
benefit in children under 2 years of age with stage C disease. In the
few children studied, levels of CMV and HIV replication appear to be independent.
This article has been cited by other articles:
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S. D. Lawn, S. T. Butera, and T. M. Folks Contribution of Immune Activation to the Pathogenesis and Transmission of Human Immunodeficiency Virus Type 1 Infection Clin. Microbiol. Rev., October 1, 2001; 14(4): 753 - 777. [Abstract] [Full Text] [PDF] |
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D. MENTZER and W. KREUZ CMV coinfection and disease progression in vertically acquired HIV infection Arch. Dis. Child., August 1, 1999; 81(2): 189k - 189. [Full Text] |
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