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 in | Farmaco (Società chimica italiana : 1989) Vol. 57; no. 4; pp. 337 - 339 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier SAS
01.04.2002
Elsevier Science |
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0014-827X 1879-0569 |
DOI: | 10.1016/S0014-827X(02)01203-X |