Pa. Roques et al., CLEARANCE OF HIV-INFECTION IN 12 PERINATALLY INFECTED CHILDREN - CLINICAL, VIROLOGICAL AND IMMUNOLOGICAL DATA, AIDS, 9(12), 1995, pp. 19-26
Objective: A case of HIV infection clearance in a perinatally infected
infant has been recently reported. We report here on the molecular, b
iological and clinical features of such virus clearance in 12 children
. Design and methods: We performed a retrospective analysis of the dia
gnosis in our 6-year cohort of 188 children born to HIV-seropositive m
others. HIV-1 was detected by coculture of infant peripheral blood mon
onuclear cells (PBMC) with cord blood cells, direct culture of infant
cells, and DNA polymerase chain reaction (PCR). The children were diag
nosed three times during the first 3 months of life and then followed
up over a postnatal period of 18-36 months. Results: The 12 reverted c
hildren had at least two positive PCR in at least two amplified region
s. Among them, six were tested positive in culture/coculture assay, an
d five were treated long-term with zidovudine. Thus, seven out of 12 r
eversions cannot be attributed to antiretroviral therapy. All the viro
logical results became negative during the first year of life, and ser
ology lowered to negative values between 9 and 23 months. We could not
find any correlation between either neutralizing or antibody-dependen
t cellular cytotoxicity-mediating antibodies and HIV clearance. Conclu
sion: In our cohort, we showed that an unexpected number of children b
orn to HIV-seropositive mothers (6.7%) cleared HIV infection during th
e first year of life, and subsequently became seronegative. Interestin
gly, most of these children exhibited unspecified clinical signs durin
g the first months of life. Five of these children were tested positiv
e only by PCR, which suggests a low virus load and could, at least par
tly, explain spontaneous clearance. However, 4 years later, among the
seven remaining infants, two seronegative children presented recurrent
hepatosplenomegaly, which may indicate the presence of hidden virus n
ot detectable by peripheral blood testing.