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Antimicrobial Agents and Chemotherapy, January 2000, p. 173-177, Vol. 44, No. 1
Department of Experimental Medicine,
University of Rome Tor Vergata,1 and
Istituto di Ricovero e Cura a Carattere Scientifico Lazzaro
Spallanzani,4 Rome, Italy; Welsh School
of Pharmacy, University of Wales College, Cardiff, United
Kingdom2; and Rega Institute for
Medical Research, Katholieke Universiteit Leuven, Leuven,
Belgium3
Received 14 June 1999/Returned for modification 22 September
1999/Accepted 18 October 1999
The anti-human immunodeficiency virus (HIV) activity of
aryloxyphosphoramidate protides of a number of anti-HIV nucleoside analogues was assessed in resting primary monocyte-macrophages (M/M).
While 2',3'-dideoxythymidine (d4T), 2',3'-dideoxyadenosine (ddA), and
2',3'-dideoxy-2',3'-didehydroadenosine (d4A) protides showed an
anti-HIV activity that was 25- to 625-fold greater than the parent
nucleotides d4T, ddA, and d4A, respectively, other aryloxyphosphoramidate protides showed similar or even lower anti-HIV activities than their parent compounds. This variable anti-HIV effect
is most likely related to the different dynamics of intracellular nucleoside monophosphate release from the protides. Our results indicate the potential advantage of therapeutic use of this approach for some nucleotide analogues to affect HIV replication in M/M, one of
the major reservoirs of HIV in vivo.
0066-4804/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Activities of Masked 2',3'-Dideoxynucleoside
Monophosphate Derivatives against Human Immunodeficiency Virus in
Resting Macrophages
*
Corresponding author. Mailing address: Department of
Experimental Medicine, University of Rome Tor Vergata, via di Tor
Vergata 135, 00133 Rome, Italy. Phone: 39-06-72596553. Fax:
39-06-72596552. E-mail: Cf.perno{at}uniroma2.it.
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