CYTOTOXIC T-LYMPHOCYTES AND ANTIBODIES AFTER ORTHOTROPIC PENETRATING KERATOPLASTY IN RATS TREATED WITH DICHLOROMETHYLENE DIPHOSPHONATE ENCAPSULATED LIPOSOMES

Citation
G. Vanderveen et al., CYTOTOXIC T-LYMPHOCYTES AND ANTIBODIES AFTER ORTHOTROPIC PENETRATING KERATOPLASTY IN RATS TREATED WITH DICHLOROMETHYLENE DIPHOSPHONATE ENCAPSULATED LIPOSOMES, Current eye research (Print), 17(10), 1998, pp. 1018-1026
Citations number
27
Categorie Soggetti
Ophthalmology
ISSN journal
02713683
Volume
17
Issue
10
Year of publication
1998
Pages
1018 - 1026
Database
ISI
SICI code
0271-3683(1998)17:10<1018:CTAAAO>2.0.ZU;2-V
Abstract
Purpose. To investigate the immunological basis for the prolonged corn eal allograft survival after subconjunctival injections of liposomes f illed with dichloromethylene diphosphonate (Cl2MDP-LIP). Methods. F344 rats received orthotropic DA corneal grafts. One group of rats was tr eated with subconjunctival injections of Cl2MDP-LIP on days 0, 2, 4, 6 and 8 postoperatively, the control groups received no treatment. Nine teen or 42 days postoperatively cytotoxic T lymphocyte (CTL) activity was measured in the lymph nodes draining the grafted and the contralat eral eyes, in the spleen and the mesenteric lymph nodes Sera taken at the same time points were tested for presence of lyric alloantibodies. Results. On day 19 CTL activity in submandibular lymph nodes draining the grafted eyes was similar in the 2 groups. In the mesenteric lymph nodes high CTL activity was found in the untreated rats and low in th e Cl2MDP-LIP rats. The spleen showed high CTL activity in the untreate d group but no activity in the liposome group. Forty two days postoper atively a decline in CTL activity was seen in both groups. Complement dependent anti-donor antibodies were absent in the Cl2MDP-LIP group at both time points whereas antibodies were present on days 19 and 42 in the untreated group. Conclusions. Repeated subconjunctival injection of Cl2MDP-LIP restricts the induction of cellular cytotoxicity against donor antigens to the regional lymph nodes and suppresses cytotoxic a ntibody formation.