The local and systemic secretion of the pro-inflammatory cytokine interleukin-6 after transplantation of retinal pigment epithelium cells in a rabbitmodel
V. Enzmann et al., The local and systemic secretion of the pro-inflammatory cytokine interleukin-6 after transplantation of retinal pigment epithelium cells in a rabbitmodel, CURR EYE R, 21(1), 2000, pp. 530-534
The rejection of retinal pigment epithelium (RPE) allografts is one of the
major problems for long-term success after retinal transplantation. However
, the details of the immunological interactions in the subretinal space aft
er transplantation are still unknown. The aim of our study was to investiga
te the role of IL-6 in the rejection process in the subretinal space and to
use IL-6 monitoring for a possible early sign of rejection after transplan
tation of allogeneic RPE cells. For this we used a model of transplanting p
igmented RPE cells, either activated in vitro with 1000 U/ml interferon-gam
ma (IFN-gamma) for 8 days or non-activated, into 30 albino rabbits. The IL-
6 was investigated 3, 5, 7, 9 and 14 days after transplantation. Additional
ly, sham operated animals and the untreated eyes served as controls. At the
se time-points the animals were killed, the liquid in the vitreous cavity a
nd serum was collected and the IL-6 present in these samples was quantified
with an enzyme-linked immunosorbent assay. Under these conditions, IL-6 wa
s detected in the liquid of the vitreous cavity and in the serum of all RPE
-transplanted rabbits. In the group receiving activated RPE two cytokine pe
aks were measured, 3 and 7 days after transplantation in the vitreous cavit
y. In non-activated grafts, a maximum was detected on the 5th day after tra
nsplantation. Generally, the detected quantity of IL-6 depended on the host
status and on the phase of rejection. No significant changes were seen in
the sera from either group. Possibly, the host RPE cells are the main sourc
e of this interleukin in the transplantation area. The measuring of IL-6 in
the rejection model suggests that it plays a role in the immune cascade in
the subretinal space.