02129nas a2200253 4500000000100000008004100001260000900042653002700051653002800078653002100106653001900127653001100146653001800157653001400175653001600189100001300205700001600218700001600234245008200250300001100332490000700343520151100350022001401861 2002 d c200210aAdjuvants, Immunologic10aAngiogenesis Inhibitors10aAntiviral Agents10aHIV Infections10aHumans10aImmune System10aNeoplasms10aThalidomide1 aDredge K1 aMarriott BJ1 aDalgleish A00aImmunological effects of thalidomide and its chemical and functional analogs. a425-370 v223 a

Thalidomide has recently shown considerable promise in the treatment of a number of conditions, such as leprosy and cancer. Its effectiveness in the clinic has been ascribed to wide-ranging properties, including anti-TNF-alpha, T-cell costimulatory and antiangiogenic activity. Novel compounds with improved immunomodulatory activity and side effect profiles are also being evaluated. These include selective cytokine inhibitory drugs (SelCIDs), with greatly improved TNF-alpha inhibitory activity, and immunomodulatory drugs (IMiDs) that are structural analogs of thalidomide, with improved properties. A third group recently identified within the SelCID group, with phosphodiesterase type 4-independent activity, is in the process of being characterized in laboratory studies. This review describes the emerging immunological properties of thalidomide, from a historical context to present-day clinical applications, most notably in multiple myeloma but also in other cancers, inflammatory disease, and HIV. We also describe the laboratory studies that have led to the characterization and development of SelCIDs and IMiDs into potentially clinically relevant drugs. Early trial data suggest that these novel immunomodulatory compounds may supercede thalidomide to become established therapies, particularly in certain cancers. Further evidence is required, however, to correlate the clinical efficacy of these compounds with their known immunomodulatory, antiangiogenic, and antitumor properties.

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