» Articles » PMID: 2452254

Immunorestorative Properties of Isoprinosine in the Treatment of Patients at High Risk of Developing ARC or AIDS

Overview
Date 1987 Dec 1
PMID 2452254
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

We have evaluated the immunomodulatory effects of isoprinosine in a double blind randomized clinical study on 63 immunosuppressed male homosexuals with persistent generalized lymphadenopathy (PGL) or ARC. The subjects received either placebo or isoprinosine at 1 or 3 g/day for 28 days. All subjects were monitored for performance for a one year period. In the 3 g/day treatment group clinical improvement was reported by 52% of the patients in contrast to 15% in the placebo group. Patients receiving 3 g/day isoprinosine showed significant increase in NK cells, a major subset of which bears the Leu 7 surface antigen, and in NK cell function as early as at the termination of treatment. This normalized NK cell property was still evident 5 months after cessation of therapy. Total T lymphocytes and T helper cells also increased in this group and a concomitant reduction was observed in activated T lymphocytes (HLA-DR+). As a direct result of the therapy an increase was found in the Th regulatory (Leu 3+ Leu 8+) cell population resulting in normalization of Th inducer/Th regulatory cell ratio. A concomitant reduction to normal range occurred in Ts effector (Leu 2+ Leu 8-) and functionally activated Ts (Leu 2+ HLA-DR+) cell populations. The kinetics of these effects suggest that isoprinosine stimulates the production of precursor lymphocytes and initiates a process of cell differentiation capable of producing long-term restoration of host immunity.

Citing Articles

The Gut Connection: Exploring the Possibility of Implementing Gut Microbial Metabolites in Lymphoma Treatment.

Al-Khazaleh A, Chang D, Munch G, Bhuyan D Cancers (Basel). 2024; 16(8).

PMID: 38672546 PMC: 11048693. DOI: 10.3390/cancers16081464.


The Fight against the Carcinogenic Epstein-Barr Virus: Gut Microbiota, Natural Medicines, and Beyond.

Eladwy R, Vu H, Shah R, Li C, Chang D, Bhuyan D Int J Mol Sci. 2023; 24(2).

PMID: 36675232 PMC: 9862477. DOI: 10.3390/ijms24021716.


Inosine Pranobex Deserves Attention as a Potential Immunomodulator to Achieve Early Alteration of the COVID-19 Disease Course.

Beran J, Spajdel M, Sliva J Viruses. 2021; 13(11).

PMID: 34835052 PMC: 8619495. DOI: 10.3390/v13112246.


Inosine Pranobex: A Key Player in the Game Against a Wide Range of Viral Infections and Non-Infectious Diseases.

Sliva J, Pantzartzi C, Votava M Adv Ther. 2019; 36(8):1878-1905.

PMID: 31168764 PMC: 6822865. DOI: 10.1007/s12325-019-00995-6.


Effects of Isoprinosine on Echinococcus multilocularis and E. granulosus metacestodes.

Sarciron M, Walbaum S, Petavy A Parasitol Res. 1995; 81(4):329-33.

PMID: 7542767 DOI: 10.1007/BF00931540.