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Virus Res ; 93(1): 31-9, 2003 May.
Article in English | MEDLINE | ID: mdl-12727340

ABSTRACT

A flow cytometric assay that measures binding of human T-lymphotropic virus type 1 (HTLV-1) virions to target cells was used to investigate the binding process and to screen for compounds affecting viral binding. Results showed that adenosine receptor type 2 antagonists effectively inhibit viral binding at concentrations below 10 microM; no inhibition was seen when antagonist was used to pretreat cells or was added post binding, suggesting direct interference with virus attachment. Efficient HTLV-1 binding required divalent calcium ions and temperatures greater than 20 degrees C. Disruption of lipid rafts by cholesterol depletion compromised viral binding but cleavage of glycosyl-phosphatidylinositol linkages had no effect. A monoclonal antibody (mAb) that recognizes HTLV-1 envelope positions 190-209 impaired binding of virus while other anti-envelope antibodies had no effect. These findings place major constraints on the nature of the HTLV-1 cell binding process and identify a class of inhibitors that may have potential for treatment of infection.


Subject(s)
2-Chloroadenosine/pharmacology , Adenosine-5'-(N-ethylcarboxamide)/pharmacology , Adenosine/analogs & derivatives , Adenosine/pharmacology , Calcium/pharmacology , Human T-lymphotropic virus 1/physiology , Purinergic P1 Receptor Agonists , T-Lymphocytes/virology , Antibodies, Monoclonal/pharmacology , Cations, Divalent/isolation & purification , Cell Line, Transformed , Human T-lymphotropic virus 1/drug effects , Human T-lymphotropic virus 1/immunology , Humans , Kinetics , Membrane Microdomains/immunology , Membrane Microdomains/virology , Phenethylamines/pharmacology , Quinazolines/pharmacology , T-Lymphocytes/drug effects , Thermodynamics , Triazoles/pharmacology
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