HOW VALUABLE ARE IGA AND IGM ANTI-HIV TESTS FOR THE DIAGNOSIS OF MOTHER-CHILD TRANSMISSION OF HIV IN AN AFRICAN SETTING

Citation
Jlk. Mokili et al., HOW VALUABLE ARE IGA AND IGM ANTI-HIV TESTS FOR THE DIAGNOSIS OF MOTHER-CHILD TRANSMISSION OF HIV IN AN AFRICAN SETTING, Clinical and diagnostic virology, 5(1), 1996, pp. 3-12
Citations number
31
Categorie Soggetti
Virology
ISSN journal
09280197
Volume
5
Issue
1
Year of publication
1996
Pages
3 - 12
Database
ISI
SICI code
0928-0197(1996)5:1<3:HVAIAI>2.0.ZU;2-F
Abstract
Background: Babies born to HIV-infected mothers retain anti-HIV of mat ernal origin until 15-18 months of age. Because of this, HIV proviral DNA and p24 antigen measurements have become the methods of choice for timely diagnosis of HIV infection in infancy. They are, however, too expensive for widespread use in the developing world. Objective: To ev aluate a simple, inexpensive serological method for diagnosing mother- child transmission of HIV, in an African population, which takes accou nt of the effects of placental transfer of maternal antibody and conti nued exposure to HIV through breast-feeding. Study Design: Plasma spec imens for a prospective study of mother-to-infant transmission of HIV in rural Zaire were collected at birth, 3, 6, 9, 12, 18 and 24 months from 21 infected infants (PP group), 21 uninfected infants (PN group) born to seropositive mothers and 21 control infants (NN group) born to uninfected mothers. The specimens were retrospectively tested for IgG , IgM and IgA anti-HIV by immunoglobulin class-specific capture EIAs, and by a commercial anti-HIV EIA. Results: In neonatal specimens, IgA and IgM anti-HIV were present, respectively, in 13 of 14 (97%) and 8 o f 14 (57%) of the PP group and in 6 of 11 (55%) and 2 of 11 (18%) of t he PN group. Later, at 3 months and older, IgA and IgM anti-HIV were o nly detected in the PP group. They peaked at 18 months (93%) and 24 mo nths (67%) respectively. Of the 21 PP group children, 8 (38%) were tra nsiently IgG anti-HIV-negative in the first year, indicating that infe ction had probably taken place after birth; four of the 8 had no detec table IgA anti-HIV during the first year. None of the specimens collec ted from the NN group babies were reactive for IgA, IgM or IgG anti-HI V. Conclusions: IgA and IgM anti-HIV may be passively transferred acro ss the placenta. Where breast-feeding is prevalent, about half of the transmissions may occur after birth, thus delaying the diagnosis of mo ther-child transmission. Nevertheless, this simple, cheap IgA anti-HIV , EIA identified 65% of transmissions by 9 months of age, and 93% at 1 8 months of age. It is a more useful marker than IgM anti-HIV, and gav e a much more rapid answer than did tests for IgG anti-HIV seroreversi on.