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.