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Antimicrobial Agents and Chemotherapy, October 1998, p. 2482-2491, Vol. 42, No. 10
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Restoration of Immune Response by a Cationic Amphiphilic Drug (AY 9944) In Vitro: A New Approach To Chemotherapy against Human Immunodeficiency Virus Type 1

Ammar Achour,1,* Jean-Charles Landureau,1 Rosangela Salerno-Concalves,2 Jean-Claude Mazière,3 and Daniel Zagury1

Université Pierre et Marie Curie, 75252 Paris,1 Laboratory of Tumor Immunology, Hôpital Laënec, Université René Descartes, 75007 Paris,2 and Laboratoire de Biochimie, Faculté de Médecine d'Amiens, Université de Picardie-Jules Verne, 80054, Amiens,3 France

Received 5 December 1997/Returned for modification 14 March 1998/Accepted 25 June 1998

AY 9944 [AY; trans-1,4-bis(chlorobenzylaminomethyl)-cyclohexane dihydrochloride], an inhibitor of sterol synthesis, was found to help restore the normal mitogenic responses and cytokine profiles of peripheral mononuclear cells (PBMCs) from AIDS patients in vitro. Compared to untreated cells, the human immunodeficiency virus type 1 (HIV-1)-infected PBMCs precultured in the presence of AY exhibited a normal rate of either mitogen-induced or recall- and superantigen-induced proliferation. After 2 weeks in the presence of the drug, the percentage of dead CD4+ cells in HIV-1-infected cultures was comparable to that observed in uninfected cultures, while over the same time interval it increased by three- to fivefold in HIV-1-infected cultures maintained in the absence of AY. AY also stimulated by 2- to 12-fold interleukin-12 (IL-12) and (gamma interferon production. For IL-12, this effect appears to be related to an increase in corresponding IL-12 p35 and IL-12 p40 mRNA levels. Moreover, AY restored the expression of the IL-2 receptor, which was severely impaired in HIV-1-infected PBMCs. Although the drug has no direct antiviral effect (it does not significantly inhibit reverse transcriptase activity measured in vitro), it might be considered a potential therapeutic agent for HIV-infected patients, in that it may correct viral infection-related immune system defects by indirectly enhancing the level of resistance to HIV and opportunistic infections.


* Corresponding author. Mailing address: Université Pierre et Marie Curie, 4, place Jussieu-Tour 32, BP 198, 75252 Paris, France. Phone: 33 (1) 44 27 32 18. Fax: 33 (1) 44 27 49 99. E-mail: achour{at}ccr.jussieu.fr.


Antimicrobial Agents and Chemotherapy, October 1998, p. 2482-2491, Vol. 42, No. 10
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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