Selective targeting of Kupffer cells with liposomal butyrate augments portal venous transfusion-induced immunosuppression

Richard V. Perez, Jeremy Johnson, Neil E. Hubbard, Kent Erickson, Murray Morgan, Sung Kim, Steven M. Rudich, Steven Katznelson, J. Bruce German

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Background. Enhanced Kupffer cell production of the immunosuppressive arachidonic acid metabolite prostaglandin E2 (PGE2) has been shown to be a mechanism of the immunosuppressive effect of portal venous transfusions- (PVT). Butyrate, a four carbon short-chain fatty acid, has received increased attention because of its ability to enhance gene transcription. This study tested the hypothesis that the intra-hepatic delivery of butyrate enhances Kupffer cell PGE2 production and thus augments the immunosuppressive effect of PVT. Methods. Butyrate was incorporated into liposomes and administered intravenously to Lewis rats. Control rats were administered intravenously to Lewis rats. Control rats were administered liposomes without butyrate. Twenty-four hours after liposome injection, rats were administered a PVT of 1 ml of Wistar-Furth blood. Kupffer cells were isolated, and PGE2 and tumor necrosis factor-α levels were measured in the culture medium after 24 hr. Additionally, Kupffer cells from butyrate-treated and control animals were added to one-way mixed lymphocyte reaction cultures. Results. Intrahepatic delivery of butyrate via liposomes increased Kupffer cell PGE2 (3800±1220 vs. 1010±119 pg/ml, P<0.05) and decreased tumor necrosis factor-α (1670±81 vs. 3360±415 pg/ml, P<0.01) production as compared with controls. Butyrate also augmented the Kupffer cell-mediated immunosuppression as demonstrated by significant depression of the mixed lymphocyte reaction (690±119 vs. 3850±148 cpm, P<0.01). Conclusion. The results support the hypothesis that intrahepatic delivery of butyrate enhances Kupffer cell PGE2 production, and specific targeting of Kupffer cells with liposomes containing immuno- modulating agents such as butyrate may be a useful means of augmenting immunosuppression protocols in organ transplantation.

Original languageEnglish (US)
Pages (from-to)1294-1298
Number of pages5
JournalTransplantation
Volume65
Issue number10
DOIs
StatePublished - May 27 1998

ASJC Scopus subject areas

  • Transplantation
  • Immunology

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