Perinatal infection by human immunodeficiency virus type 1 (HIV-1): relationship between proviral copy number in vivo, viral properties in vitro, and clinical outcome

J Med Virol. 1991 Dec;35(4):283-9. doi: 10.1002/jmv.1890350414.

Abstract

Human immunodeficiency virus type 1 (HIV-1) isolates from 25 perinatally HIV-1 infected children were classified according to their capacity to replicate in vitro as rapid (R), intermediate (S/R) and slow (S) variants. R-type viruses replicated on peripheral blood mononuclear cells (PBMCs) and grew better in T-lymphoid cells, even though 9 out of 12 isolates also maintained tropism for monocytoid cells. The S/R-type isolates replicated efficiently after several days of culture, while the S-type viruses displayed only a low and transient replication activity; however, both S/R- and S-type isolates exerted viral transactivation activity in an indicator monocytoid cell line. Replication patterns in vitro were significantly associated in vivo with the number of HIV-1 copies in PBMCs as determined by polymerase chain reaction: in children with R-type isolates, the number of HIV-1 proviral DNA molecules/10(5) PBMCs ranged from 62 to 571, and in children with S/R and S isolates the range was 5-43. Seven children had severe symptomatic HIV-1 infection, and in all an R-type virus was identified; 18 children had no or only mild symptoms, and among these, S-, S/R-, and R-type isolates were found in 5, 8, and 5 cases, respectively. Besides demonstrating HIV-1 variability in perinatal infection, these findings suggest that R-type virus might be a prerequisite for disease progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Child
  • Child, Preschool
  • Clone Cells
  • Female
  • Genetic Variation
  • HIV Infections / genetics
  • HIV Infections / microbiology*
  • HIV Infections / transmission
  • HIV-1 / genetics
  • HIV-1 / growth & development
  • HIV-1 / pathogenicity*
  • Humans
  • Infant
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / microbiology
  • Maternal-Fetal Exchange
  • Organ Specificity
  • Polymerase Chain Reaction
  • Pregnancy
  • Pregnancy Complications, Infectious / microbiology*
  • Prognosis
  • Proviruses / genetics
  • Proviruses / pathogenicity*
  • Transcriptional Activation
  • Virus Replication*