COMBINED LIVER-SPLEEN-SMALL INTESTINE GRAFTING IN A RAT MODEL - ROLE OF TRANSPLANTING ADDITIONAL LYMPHOID-TISSUE ON SURVIVAL

Citation
M. Dsilva et al., COMBINED LIVER-SPLEEN-SMALL INTESTINE GRAFTING IN A RAT MODEL - ROLE OF TRANSPLANTING ADDITIONAL LYMPHOID-TISSUE ON SURVIVAL, International surgery, 81(2), 1996, pp. 109-114
Citations number
27
Categorie Soggetti
Surgery
Journal title
ISSN journal
00208868
Volume
81
Issue
2
Year of publication
1996
Pages
109 - 114
Database
ISI
SICI code
0020-8868(1996)81:2<109:CLIGIA>2.0.ZU;2-K
Abstract
The aim of this study was to develop suitable models of combined intes tinal grafting to examine the enhancing effect of intestinal grafting with additional lymphoid tissue using 30% of the liver mass and the wh ole spleen on recipient survival in the absence of immunosuppression, Grafts from DA (RTI(a)) rats were transplanted orthotopically to PVG ( RT1(1)) recipients according to the following design: group 1 (n=6), e n bloe 30% liver/entire SB/spleen; group 2 (n=7), en bloc 30% liver/SB ; group 3 (n=7), SB/spleen and group 4 (n=7), SE control for the prece ding groups, The orthotopic nature and proximal interposition of the S B graft allowed the assessment of protection afforded by components of the cluster on the SB graft using survival endpoints. Although group 4 hosts survived half as long compared to other groups, statistical si gnificance was reached only in the case of group 1; group 1 MST equall ed 15.3 days, significantly higher than group 4 (p=0.01). Acute reject ion was present in every grafted tissue and was equivalent whether liv er was included or excluded in the cluster GVHD was absent postoperati vely using clinical or histological criteria; recipient spleens showed hyperplasia, donor spleens depicted lymphocytic depletion on histolog y. This study determined that statistically proven enhanced survival w as obtained only after grafting 30% liver plus spleen with the entire SE. GVHD was rare in the fully allogeneic system despite transplanting a massive load of lymphoid tissue. The surgical models used in this s tudy employing liver in the cluster, address the important question of how best to evaluate the role of heterotopic accessory liver grafting in providing tolerance to co-transplanted small intestine.