Important note: Information in this article was accurate in 1992. The state of the art may have changed since the publication date.
IMUTHIOL, A T-CELL SPECIFIC IMMUNOPOTENTIATOR
Int J Immunotherapy; 6(1):25-35 1990. Unique Identifier : AIDSLINE ICDB/92669937 Renoux G; Renoux M; Immunology Lab., Faculty of Medicine, 37032 Tours, France
Abstract:
Imuthiol (Institut Merieux, Lyon, France), purified sodium diethyldithiocarbamate (Ditiocarb, DTC), evinces distinctive properties, not actually shared by other biologicals. Imuthiol recruits T cells from precursors and activates T-cell functions, including interleukin-2 production and NK activity, without time- and dose-dependent inhibitory effects. It modifies MHC-encoded antigens on the T-cell surface. Imuthiol is also an anti-inflammatory agent; its mechanisms of action involve a brain neocortex control. Imuthiol regulates microsomal enzyme activities. It inhibits metalloenzymes in microorganisms or neoplastic cells without affecting normal mammalian cells. It protects against the toxicities of chemicals, and it has antibiotic effects. Imuthiol improves the clinical status and restores T-cell numbers and functions in patients (pts) affected with ailments associated with T-cell deficit or dysfunction (elderly, chronic infection, tuberculosis, surgery, cancer, autoimmune diseases, etc), without untoward effects. Importantly, Imuthiol inhibits HIV reverse transcriptase. It increases the CD4+ population and induces long-lasting clinical improvement in pts with AIDS-related complex. Thus, Imuthiol, a non-toxic and T-cell specific immunopotentiator, can be used to treat pts with incipient HIV infection. (62 Refs)
Keywords: Acquired Immunodeficiency Syndrome/DRUG THERAPY Adult Aged Animal AIDS-Related Complex/DRUG THERAPY Child Ditiocarb/*THERAPEUTIC USE Dose-Response Relationship, Drug Double-Blind Method Human Immunologic Deficiency Syndromes/*DRUG THERAPY Neoplasms/DRUG THERAPY Opportunistic Infections/DRUG THERAPY T-Lymphocytes/*DRUG EFFECTS JOURNAL ARTICLE CLINICAL TRIAL MULTICENTER STUDY RANDOMIZED CONTROLLED TRIAL REVIEW 921230
M92C5383
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