Document 0537 DOCN M9550537 TI Increased soluble CD8 (sCD8) in human immunodeficiency virus 1-infected children in the first month and year of life. DT 9505 AU Gesner M; Di John D; Krasinski K; Borkowsky W; Department of Pediatrics, New York University Medical Center, NY; 10016. SO Pediatr Infect Dis J. 1994 Oct;13(10):896-8. Unique Identifier : AIDSLINE MED/95158128 AB The purpose of this study was to determine whether soluble CD8 (sCD8) in serum of perinatally human immunodeficiency virus 1 (HIV-1)-infected children during the first year of life differs from that of HIV-1-uninfected control children. Soluble CD8 concentrations in stored plasma and serum samples of children of HIV-1-infected and uninfected mothers were determined using a sandwich immune assay. In the first month of life significantly greater concentrations of sCD8 occurred in 12 HIV-1-infected infants than in 9 uninfected infants born to infected mothers (mean = 1054, SD 540 vs. 589, SD 370 units/ml, P < 0.05), although the CD8+ T cell proportions were not different (21.7 vs. 21.1, P > 0.5). The difference in sCD8 concentrations was most pronounced in 8 infants who were HIV-1 culture positive on initial testing in the first week of life compared with the remaining 4 patients when virus was first detected on subsequent analysis (mean = 1315, SD 446 vs. 529, SD 231 units/ml, P < 0.01). The concentration of sCD8 was also greater in 26 HIV-1-infected children than in either 26 uninfected children born to infected mothers or 25 seronegative children during the first year of life (mean = 1268, SD 529 vs. 630, SD 290 vs. 553, SD 315 units/ml, P < 0.05). Early and persistent elevation in sCD8 probably reflects immune activation resulting from HIV-1 infection. The occurrence of this increase in the neonatal period may reflect prenatal viral transmission, a higher viral inoculum or coinfection with other agents stimulating immune activation. DE Analysis of Variance AIDS Serodiagnosis Case-Control Studies Cross-Sectional Studies CD8-Positive T-Lymphocytes/*IMMUNOLOGY Disease Transmission, Vertical Human HIV Infections/*CONGENITAL/*IMMUNOLOGY/TRANSMISSION HIV-1/*IMMUNOLOGY Infant Infant, Newborn Retrospective Studies Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocyte Subsets/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).