HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

CD26 expression correlates with entry, replication and cytopathicity of monocytotropic HIV-1 strains in a T-cell line.

Abstract
Experiments to identify cell determinants involved in HIV-1 tropism revealed a specific decrease in the expression of the T-cell activation antigen CD26 after monocytotropic (M-tropic) but not T-cell line-tropic (T-tropic) virus infection of the PM1 T-cell line. The level of CD26 expression in single-cell clones of PM1 correlated with the entry rate and cytopathicity of M-tropic HIV-1 variants, resulting in preferential survival of cells with low CD26 levels after infection. Experiments with recombinant viruses showed that the third hypervariable region of the envelope gp120 plays an important role in this selection process. This study identifies CD26 as a key marker for M-tropic human immunodeficiency virus type 1 (HIV-1) infection and suggests a mechanism for the early loss of CD26-expressing cells in HIV-1-infected individuals.
AuthorsT Oravecz, G Roderiquez, J Koffi, J Wang, M Ditto, D C Bou-Habib, P Lusso, M A Norcross
JournalNature medicine (Nat Med) Vol. 1 Issue 9 Pg. 919-26 (Sep 1995) ISSN: 1078-8956 [Print] United States
PMID7585218 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • DNA, Viral
  • HIV Envelope Protein gp120
  • HIV envelope protein gp120 (305-321)
  • Peptide Fragments
  • RNA, Messenger
  • Receptors, Virus
  • Dipeptidyl Peptidase 4
Topics
  • Amino Acid Sequence
  • Base Sequence
  • CD4-Positive T-Lymphocytes (enzymology, virology)
  • Cell Survival
  • Cells, Cultured
  • Cytopathogenic Effect, Viral
  • DNA, Viral (analysis)
  • Dipeptidyl Peptidase 4 (biosynthesis, genetics, physiology)
  • Down-Regulation
  • Gene Expression Regulation, Viral
  • HIV Envelope Protein gp120 (metabolism)
  • HIV Infections (immunology, pathology, virology)
  • HIV-1 (pathogenicity, physiology)
  • Humans
  • Molecular Sequence Data
  • Monocytes (virology)
  • Peptide Fragments (metabolism)
  • RNA, Messenger (biosynthesis)
  • Receptors, Virus
  • Virus Replication

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: