CD8(+) T cell-mediated suppression of human immunodeficiency virus replication in older children with acquired immunodeficiency syndrome

Citation
B. Salimi et al., CD8(+) T cell-mediated suppression of human immunodeficiency virus replication in older children with acquired immunodeficiency syndrome, PEDIAT INF, 19(2), 2000, pp. 109-113
Citations number
19
Categorie Soggetti
Clinical Immunolgy & Infectious Disease
Journal title
PEDIATRIC INFECTIOUS DISEASE JOURNAL
ISSN journal
08913668 → ACNP
Volume
19
Issue
2
Year of publication
2000
Pages
109 - 113
Database
ISI
SICI code
0891-3668(200002)19:2<109:CTCSOH>2.0.ZU;2-J
Abstract
Background. Suppression of HIV replication by CD8(+) T cells and/or their p roducts correlated with the survival of infants. We sought to elucidate the role of CD8(+) T cell-mediated suppression in seven older children with AI DS. Methods. After separation of each child's CD4(+) and CD8(+) T cells, three different HIV culture assays were performed: (1) patient CD4(+) T cells and phytohemagglutinin (PHA)-stimulated donor peripheral blood mononuclear cel ls (PBMC); (2) patient CD8(+) T cells added to the CD4(+) T cells and the P HA-stimulated donor PBMC (to test for CD8-mediated T cell suppression of HI V); (3) patient CD8(+) cells added across a semipermeable membrane to the C D4(+) T cells and the PHA-stimulated donor PBMC [to determine whether the C D8 cells secreted a soluble factor(s) that suppressed HIV]. Results. Cultures from four of seven children showed greater HIV replicatio n with CD4 cells alone than with CD4 and CD8 cells together, demonstrating CD8 suppression; evidence of soluble suppression was also seen. Cultures fr om two of the seven children showed HIV replication and no evidence of CD8 cell suppression. Cultures from one of the seven children had no appreciabl e replication of HIV even after removal of CD8 cells. Conclusions. CD8-mediated suppression is present in at least some children with AIDS. Additional mechanisms may be operating to slow the progression o f the disease.