Inhibition of activated murine T-lymphocytes by synthetic glycoglycerolipid analogues

Glycoglycerolipid analogues, characterized by a glycerol aglicone β-linked in position 2 to a glucose or galactose residue, and by a lipophilic C 6 acyl chain on the glycerol unit, significantly inhibit proliferation of activated T cells. The inhibitory activity displayed by such synthetic compounds...

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Published inFarmaco (Società chimica italiana : 1989) Vol. 57; no. 4; pp. 337 - 339
Main Authors Colombo, Diego, Ronchetti, Fiamma, Toma, Lucio, Pisano, Barbara, Ianaro, Angela
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier SAS 01.04.2002
Elsevier Science
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Summary:Glycoglycerolipid analogues, characterized by a glycerol aglicone β-linked in position 2 to a glucose or galactose residue, and by a lipophilic C 6 acyl chain on the glycerol unit, significantly inhibit proliferation of activated T cells. The inhibitory activity displayed by such synthetic compounds is comparable to the immunosuppressive properties shown by the natural glycolipids simplexides, to which they are structurally related. Vice versa, when the acyl chain is located on the sugar unit, no immunomodulating activity is observed, suggesting a strict relationship between the activity and the location of the acyl chain.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0014-827X
1879-0569
DOI:10.1016/S0014-827X(02)01203-X