FIV infection of macrophages: in vitro and in vivo inhibition by dideoxycytidine 5′-triphosphate

We have evaluated in vitro and in vivo whether it is possible to protect cat macrophages from feline immunodeficiency virus (FIV) infection by the administration of dideoxycytidine 5′-triphosphate (DDCTP). Since cell membranes are impermeable to phosphorylated drugs we have encapsulated DDCTP into a...

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Veröffentlicht in:Veterinary immunology and immunopathology 1995-05, Vol.46 (1), p.151-158
Hauptverfasser: Magnani, M., Rossi, L., Fraternale, A., Silvotti, L., Quintavalla, F., Piedimonte, G., Matteucci, D., Baldinotti, F., Bendinelli, M.
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container_end_page 158
container_issue 1
container_start_page 151
container_title Veterinary immunology and immunopathology
container_volume 46
creator Magnani, M.
Rossi, L.
Fraternale, A.
Silvotti, L.
Quintavalla, F.
Piedimonte, G.
Matteucci, D.
Baldinotti, F.
Bendinelli, M.
description We have evaluated in vitro and in vivo whether it is possible to protect cat macrophages from feline immunodeficiency virus (FIV) infection by the administration of dideoxycytidine 5′-triphosphate (DDCTP). Since cell membranes are impermeable to phosphorylated drugs we have encapsulated DDCTP into autologous erythrocytes and modified erythrocyte membranes to target these drug-loaded cells to macrophages. DDCTP-loaded erythrocytes reduced FIV production by macrophages infected in vitro or obtained from naturally or experimentally infected cats. The same treatment protected the majority of peritoneal macrophages during a 7 month experimental FIV infection and reduced the percentage of circulating lymphocytes stained with an anti-p24 antibody. These results suggest that the administration of nucleoside analogues in phosphorylated form is feasible and their targeting to macrophages reduces FIV infection in vitro and in vivo.
doi_str_mv 10.1016/0165-2427(94)07014-X
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Since cell membranes are impermeable to phosphorylated drugs we have encapsulated DDCTP into autologous erythrocytes and modified erythrocyte membranes to target these drug-loaded cells to macrophages. DDCTP-loaded erythrocytes reduced FIV production by macrophages infected in vitro or obtained from naturally or experimentally infected cats. The same treatment protected the majority of peritoneal macrophages during a 7 month experimental FIV infection and reduced the percentage of circulating lymphocytes stained with an anti-p24 antibody. These results suggest that the administration of nucleoside analogues in phosphorylated form is feasible and their targeting to macrophages reduces FIV infection in vitro and in vivo.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>7618255</pmid><doi>10.1016/0165-2427(94)07014-X</doi><tpages>8</tpages></addata></record>
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subjects AIDS/HIV
ANIMAL VIRUSES
Animals
ANTIVIRAL
ANTIVIRAL AGENTS
Antiviral Agents - administration & dosage
Antiviral Agents - pharmacology
CATS
CHAT
DEFICIENCE IMMUNOLOGIQUE
DEFICIENCIA INMUNOLOGICA
Deoxycytosine Nucleotides - administration & dosage
Deoxycytosine Nucleotides - pharmacology
Dideoxynucleotides
Drug Carriers
ERITROCITOS
ERYTHROCYTE
ERYTHROCYTES
Feline Acquired Immunodeficiency Syndrome - blood
Feline Acquired Immunodeficiency Syndrome - drug therapy
Feline Acquired Immunodeficiency Syndrome - immunology
feline leukemia virus
Female
GATO
Immunodeficiency Virus, Feline - drug effects
Immunodeficiency Virus, Feline - physiology
IMMUNOLOGICAL DEFICIENCY
Lymphocytes - virology
MACROFAGOS
MACROPHAGE
MACROPHAGES
Macrophages - virology
Macrophages, Peritoneal - virology
Male
Specific Pathogen-Free Organisms
VIRICIDAS
VIRUS DE LOS ANIMALES
VIRUS DES ANIMAUX
Virus Replication - drug effects
title FIV infection of macrophages: in vitro and in vivo inhibition by dideoxycytidine 5′-triphosphate
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