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Immunopharmacol Immunotoxicol ; 10(4): 597-615, 1988.
Article in English | MEDLINE | ID: mdl-3246542

ABSTRACT

In this study the ability of prostaglandin E1 (PGE1), Misoprostol (a stable analog of PGE1), and 16,16-dimethyl PGE2 (a stable analog of PGE2) to suppress immune responses in vitro and in vivo was determined. All of the compounds caused a titratable (10(-6) to 10(-9) M) suppression of Con A blastogenesis and the mixed lymphocyte response whereas there was only slight inhibition of the LPS response. When either 16,16-dimethyl PGE2 (30 ug/mouse) or Misoprostol (60 ug/mouse) was administered daily in vivo, there was a significant suppression of splenomegaly in F1 mice (C57Bl/6 x CBA) which had been injected with parental (C57Bl/6) spleen cells. We conclude that prostaglandins of the E series can function as immunosuppressive reagents both in vitro and in vivo. In the future they may serve to augment existing forms of immunosuppressive therapy.


Subject(s)
Graft vs Host Reaction/drug effects , Prostaglandins E/pharmacology , Animals , Antibody Formation , Immunosuppression Therapy , In Vitro Techniques , Lymphocyte Activation , Male , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Prostaglandins G/analogs & derivatives , Prostaglandins G/pharmacology
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