Biologic effects after a single dose of poly(I):poly(C12U) in healthy volunteers

C W Hendrix, J B Margolick, B G Petty, R B Markham, L Nerhood, H Farzadegan, P O Ts'o, P S Lietman, C W Hendrix, J B Margolick, B G Petty, R B Markham, L Nerhood, H Farzadegan, P O Ts'o, P S Lietman

Abstract

Poly(I):poly(C12U) (mismatched double-stranded RNA; atvogen), an interferon inducer, is active against human immunodeficiency virus in vitro. To determine the extent and duration of the biologic effects of poly(I):poly(C12U), we administered a single dose of the drug to healthy volunteers in a randomized, double-blind, placebo-controlled 2-week crossover study. We analyzed blood for alpha and gamma interferons, neopterin, 2',5'-oligoadenylate synthetase, lymphocyte surface markers, lymphocyte proliferation after exposure to soluble antigens and mitogens, and natural killer cell activity. Minimal biologic effects were observed after administration of a single 200-mg dose to four volunteers; therefore, the dose was increased to 600 mg in 10 subjects. Only neopterin levels and symptoms were greater after administration of 600 mg of poly(I):poly(C12U) than after administration of placebo (Wilcoxon signed rank sum test, P = 0.06). A definite response in 2',5'-oligoadenylate synthetase activity, however, was seen in a few subjects. Neither alpha nor gamma interferon was detectable in serum after poly(I):poly(C12U) dosing. The neopterin changes after administration of poly(I):poly(C12U) were similar at both poly(I):poly(C12U) dose levels, with an early decrease at 6 h, a peak at 1 day, and a gradual decrease toward the baseline over the following 3 days. A mild flu-like syndrome occurred in one-half of the subjects following administration of poly(I):poly(C12U) and in only one subject following administration of placebo. This syndrome resolved within 16 h after poly(I):poly(C12U) dosing. We conclude that poly(I):poly(C12U) does not induce measurable levels of interferon and causes only minimal biologic or toxic effects among those parameters measured after administration of a single dose in the 200- to 600-mg dose range in health volunteers.

References

    1. J Mol Biol. 1972 Oct 14;70(3):567-87
    1. AIDS Res Hum Retroviruses. 1990 Aug;6(8):1045-9
    1. J Immunol. 1980 Apr;124(4):1852-7
    1. Lancet. 1981 Sep 5;2(8245):497-500
    1. Tex Rep Biol Med. 1981-1982;41:663-71
    1. Cancer Res. 1985 Oct;45(10):4774-8
    1. J Biol Response Mod. 1985 Oct;4(5):495-502
    1. J Infect Dis. 1992 Oct;166(4):717-22
    1. J Biol Response Mod. 1985 Dec;4(6):669-75
    1. Lancet. 1987 Apr 18;1(8538):890-2
    1. Proc Natl Acad Sci U S A. 1987 May;84(9):2985-9
    1. Lancet. 1987 Jun 6;1(8545):1286-92
    1. Clin Pharmacol Ther. 1987 Nov;42(5):567-75
    1. J Clin Invest. 1987 Dec;80(6):1631-9
    1. J Interferon Res. 1987 Oct;7(5):511-9
    1. J Gen Virol. 1987 Nov;68 ( Pt 11):2831-8
    1. Ann Intern Med. 1990 Jun 1;112(11):805-11
    1. Mol Pharmacol. 1976 Mar;12(2):299-312

Source: PubMed

3
Sottoscrivi