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Antimicrobial Agents and Chemotherapy, February 2000, p. 405-407, Vol. 44, No. 2
CEA, Service de Neurovirologie, DSV/DRM,
CRSSA, IPSC, Fontenay aux Roses,1
SPI-BIO, Massy,2 Laboratoire
d'Immunodifférenciation, Université Denis Diderot,
Paris,4 and Laboratoires
Mayoly-Spindler, Chatou,3 France
Received 5 May 1999/Returned for modification 10 August
1999/Accepted 18 October 1999
Amphotericin B derivatives, such as MS-8209, have been evaluated as
a therapeutic approach to human immunodeficiency virus (HIV) infection.
We show that MS-8209, like amphotericin B, increases tumor necrosis
factor alpha (TNF-
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Effects of MS-8209, an Amphotericin B Derivative, on Tumor
Necrosis Factor Alpha Synthesis and Human Immunodeficiency Virus
Replication in Macrophages
) mRNA expression and TNF-
production and
consequently HIV replication in human macrophages. These effects
confirm the pharmacological risk associated with the administration of
amphotericin B or its derivatives to HIV-infected patients.
*
Corresponding author. Mailing address: Service de
Neurovirologie, CEA/DSV/DRM, 60-68, avenue de la Division Leclerc, B.P. 6, 92265, Fontenay aux Roses Cedex, France. Phone: 33 (0)1 46 54 87 69. Fax: 33 (0)1 46 54 77 26. E-mail:
clayette{at}dsvidf.cea.fr.
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