XENOGENEIC HUMORAL RESPONSES TO ISLETS TRANSPLANTED IN BIOHYBRID DIFFUSION-CHAMBERS

Citation
Rp. Lanza et al., XENOGENEIC HUMORAL RESPONSES TO ISLETS TRANSPLANTED IN BIOHYBRID DIFFUSION-CHAMBERS, Transplantation, 57(9), 1994, pp. 1371-1375
Citations number
23
Categorie Soggetti
Immunology,Surgery
Journal title
ISSN journal
00411337
Volume
57
Issue
9
Year of publication
1994
Pages
1371 - 1375
Database
ISI
SICI code
0041-1337(1994)57:9<1371:XHRTIT>2.0.ZU;2-X
Abstract
It has been hypothesized that chronic antigen leakage from the hybrid artificial pancreas could stimulate a host humoral response. Such anti bodies could be induced by antigens shed from the islet cell surface, or by proteins secreted by live cells or liberated after cell death. T o determine if this humoral response occurs, porcine (n=15) or canine (n=7) islets were seeded (2-5 x 10(4) equivalent islet number, density 30 islets/mm(3)) into diffusion chambers fabricated from permselectiv e acrylic membranes (nominal M(r) exclusion of 80,000). The chambers w ere implanted intraperitoneally into streptozotocin-induced diabetic r ats. Sera were collected at various intervals (0-12 weeks) and tested against isolated canine and porcine islets, for tissue specificity and interspecies cross-reactivity by fluorescence immunocytochemistry. No immunofluorescence (or only weak background staining) was obtained wh en islets were exposed to horse sera, or to sera obtained before to xe nodevice implantation. Within 2-6 weeks, however, the postimplantation sera showed strong immunoreactivity. The antibodies were found to be reactive to multiple tissues, and to possess little or no interspecies cross-reactivity. The appearance of these xenoantibodies coincided wi th the appearance of circulating soluble immune complexes. However, no ne of the respiratory, cutaneous, or gastrointestinal manifestations t hat are characteristic of an anaphylactic reaction, or of the diseases of immediate-type hypersensitivity, were observed, even after intrape ritoneal injection of additional naked islet tissue. Renal glomeruli d id not stain for IgG or C3 in islet recipients. These results suggest that islet cell antigens crossed the membrane and stimulated antibody formation in the host, although they did not appear to cause renal or immune complex disease during the course of this study.