HIV ANTIBODY-RESPONSES IN CHILDREN OF HIV-INFECTED MOTHERS

Citation
Jl. Sever et al., HIV ANTIBODY-RESPONSES IN CHILDREN OF HIV-INFECTED MOTHERS, Pediatric AIDS and HIV infection, 7(4), 1996, pp. 246-253
Citations number
20
Categorie Soggetti
Pediatrics,Immunology
ISSN journal
10455418
Volume
7
Issue
4
Year of publication
1996
Pages
246 - 253
Database
ISI
SICI code
1045-5418(1996)7:4<246:HAICOH>2.0.ZU;2-C
Abstract
About 25% of the children of untreated HIV-infected mothers are later determined to be HIV-infected. At birth, all of the children of HIV-in fected mothers have HIV-IgG antibody, which is transferred transplacen tally from the mothers to their children, and infected children produc e HIV-IgG antibody in response to their infection. Most infected child ren have detectable HIV-IgA by 3 months of age. We have studied HIV an tibody responses in three groups of children of HIV-infected mothers a t 9 to 12 months and 15 to 24 months of age. The groups were classifie d by Centers for Disease Control and Prevention (CDC) criteria and inc luded: (I) HIV seroreverters (SR); (II) HIV-infected; Non- to mildly s ymptomatic (N+A); and (III) HIV-infected; Moderately to Severely Sympt omatic (BSC). HIV-IgG antibody was detected in some SR children at low titer levels (10 to 20) through 11 months of age but not at 12 or lat er. For both the N+A and B+C groups, there were no significant changes in the mean HIV-IgG titers from 9-12 to 15-24 months of age. Also, no significant difference in titers were found between the two infected groups for both age groups. HIV-IgA antibody responses were more frequ ently positive at 15 to 24 months for all seven antigens studied for t he N+A than the B+C patients; however, statistical significance was at tained only for gp41 (p less than or equal to 0.01). N+A children show ed more responses to the viral antigens at 15-24 months than at 9-12 m onths. This increase in HIV-specific IgA among the N+A children may be important in restricting their HIV infections. Total IgG levels were significantly higher in the HIV-infected groups than in the SR (p less than or equal to 0.0001), but no differences were detected between sh e N+A and B+C groups. Total IgA increased over lime in the N+A patient s from 9-12 to 15-24 months. A similar trend was apparent in the B+C g roup, but did not reach statistical significance, Both N+A and B+C pat ients at 15-24 months had significantly higher total IgA levels than d id the SR at 9-12 months of age. The B+C group had significantly lower CD4 counts for both age groups than did the N+A or SR groups (p less than or equal to 0.0001).