Transendothelial Migration of Lymphocytes from HIV-1-Infected Donors: A Mechanism for Extravascular Dissemination of HIV-1

Holly H. Birdsall, Joann Trial, Hsiang J. Lin, David M. Green, Glen W. Sorrentino, Edward B. Siwak, Andrew L. De Jong, Roger D. Rossen

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


To identify factors that cause HIV-1 to establish perivascular foci of infected cells, we studied the transendothelial migration of blood mononuclear leukocytes (MNL) from 76 HIV+ patients and 41 controls. The fraction of patients' lymphocytes that migrated across endothelial cell monolayers in vitro was significantly increased (p ≤ 0.03) compared with that of control donors. Migration of patients' CD4+ T cells was particularly enhanced, whereas the migration of monocytes did not differ between patients and controls. Lymphocyte migration correlated with expression of CD11a/CD18 and CD49d/CD29 and with the quantity of TNF-α produced as MNLs migrated through the endothelium. Measurement of HIV-1 proviral DNA copies in the patients' MNLs (n = 26) suggested that in half the cases virus-infected cells accumulated preferentially amidst the migratory leukocytes. We observed the same behavior with normal donor MNLs infected, in vitro, with each of 4 strains of HIV-1. The number of HIV-1 proviral DNA copies per million MNLs was 40 to 178 times higher in the migratory population than in the original population added to the endothelium. To test whether only certain strains of HIV-1 stimulate transendothelial migration of infected cells, we used single strand conformation polymorphism analysis to identify quasispecies of HIV-1 in the MNLs. If all strains of HIV-1 were equal in their ability to stimulate transendothelial migration, we expected to find no differences in the quasispecies present in the original and migratory cell populations. In fact the quasispecies differed in 14 of 19 paired samples, suggesting that only certain HIV-1 quasispecies promote transendothelial migration of infected cells.

Original languageEnglish (US)
Pages (from-to)5968-5977
Number of pages10
JournalJournal of Immunology
Issue number12
StatePublished - Jun 15 1997

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


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