BACKGROUND Standard therapy for severe, immune mediated, ocular inflammation has significant side effects, and may fail to control the disease. T cell directed monoclonal antibody (mAb) therapy can provide long term remission of inflammatory disease in experimental models. The Campath-1H mAb was administered to patients with severe, refractory, ocular inflammation.
METHODS 10 patients with severe, refractory, non-infectious ocular inflammatory disease were treated with Campath-1H mAb. This is a fully humanised mAb which recognises the pan-lymphocyte antigen CD52.
RESULTS AND DISCUSSION Following Campath-1H therapy, all 10 patients showed an initial resolution of their ocular symptoms and signs. Long lasting remissions were achieved in eight patients, in whom baseline immunosuppression could subsequently be reduced to minimal levels. The possible mechanisms of action of Campath-1H therapy are discussed.
- ocular inflammation
- monoclonal antibody therapy
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Non-infectious ocular inflammatory disease represents a wide spectrum of immune mediated pathology, which may result in severe visual handicap. In addition to numerous idiopathic inflammatory conditions specific for the eye, a number of systemic conditions, such as Wegener's granulomatosis, Behçet's disease, and sarcoidosis, also have serious ocular complications. Immunosuppression is generally effective in controlling these conditions, using systemic corticosteroids plus adjunctive therapy with cyclosporin A, cyclophosphamide, azathioprine, or newer agents such as FK-506 and mycophenolate mofetil. There is usually a requirement for chronic therapy, however, with associated toxicity, and there is also a subset of patients who are refractory to even the most aggressive regimens.1 The ideal therapy would, therefore, provide long term remission of inflammatory disease following a short course of treatment, and also be effective across the severity spectrum. In animal models of immunopathology, anti-T cell monoclonal antibody (mAb) therapy achieves such effects by inducing antigen specific unresponsiveness and immunoregulation.2 Similar immunomodulatory mAb therapy has been used in patients with aggressive autoimmune and inflammatory diseases and, occasionally, long term responses have followed short term treatment. Campath-1H is a humanised mAb which recognises the pan-lymphocyte antigen CD52,3 4and which has been used in such circumstances. Beneficial effects were transient in some conditions, such as rheumatoid arthritis,5 but were longstanding in others such as multiple sclerosis.6 In cases of severe refractory vasculitis, remissions of several years' duration were achieved.7 In addition, single case studies have reported the success of Campath-1H therapy in controlling severe posterior uveitis8 and in preventing recurrent corneal graft rejection,9 both cases refractory to conventional immunosuppression. We now present data on a cohort of 10 patients treated with Campath-1H for severe, refractory, non-infectious, immune mediated, intraocular and orbital inflammatory disease, and recurrent corneal allograft rejection.
Methods and patients
Patients with refractory, non-infectious, ocular inflammatory disease were offered therapy with Campath-1H mAb on a compassionate, “named patient”, basis. The indications for therapy are shown in Table 1. Patients 1, 3, 4, and 9 had ocular disease as a complication of a systemic inflammatory disease, although the latter was clinically inactive at the time of Campath-1H treatment. In all patients vision was already severely impaired, and was continuing to deteriorate despite conventional therapy with, most commonly, prednisolone, cyclosporin A, and azathioprine. These drugs were titrated to maximum recommended doses, unless limited by toxicity. Campath-1H was administered by intravenous infusion at 10–12 mg daily for 5 days; patients 2 and 4 received two courses of therapy. Patients were monitored closely after therapy, both ophthalmologically, and also systemically for adverse reactions.
Results and discussion
Following Campath-1H all patients showed initial improvement with an increase in visual acuity, resolved clinical inflammation, or maintenance of corneal graft clarity. In one patient (case 4) an initial improvement was followed by a relapse of disease, which was controlled with a higher dose (150 mg) of Campath-1H. Case 2 required two courses of Campath-1H (total dose of 120 mg) to suppress ongoing corneal allograft rejection. Some patients experienced a mild first dose reaction but toxicity was otherwise minimal, and no patient sustained refractory and/or opportunistic infections. Furthermore, it was usually possible to substantially reduce baseline immunosuppression after Campath-IH.
These data suggest that ocular immunoinflammatory disease is a particularly sensitive target for T cell mAb therapy. Despite progressive, sight threatening pathologies refractory to treatment, remission was achieved with Campath-1H therapy in eight of 10 patients. It was then possible to reduce baseline immunosuppression to very low levels. Disease was stabilised, and became easier to control in the remaining two patients (cases 8 and 9). The mechanism by which Campath-1H achieved these effects is currently unknown. Infectious tolerance in animal models is achieved with non-depleting mAbs, and invokes regulatory mechanisms that seem to operate within the antigen presenting cell microenvironment but which have not yet been fully defined.2 In contrast, Campath-1H is a lymphocytotoxic mAb and, while total peripheral blood lymphocyte (PBL) numbers return to normal after therapy, there is a protracted reduction in CD4+ PBL counts, with inversion of the CD4:CD8 ratio. It is conceivable that Campath-1H facilitates the re-establishment of ocular immunoregulation by altering lymphocyte subset ratios, but both autoaggressive and regulatory T cells reside within the CD4+ subset2 and, without more specific markers for these cells, it will remain difficult to explain the beneficial effects of Campath-1H.10Additionally, until its actions are more fully understood, this treatment should not be viewed as a panacea for non-infectious ocular immuno-inflammatory disease. Although the long term lymphopenia that follows Campath-1H therapy has not been linked to an increased risk of infection or malignancy in any of the conditions treated, follow up remains relatively short. Notwithstanding such reservations, Campath-IH appears to be a very useful agent in ocular inflammation and we would encourage its further application, on an experimental basis, in difficult and refractory cases.
We are indebted to our consultant colleagues, Mr Miles Stanford and Dr Elizabeth Graham, for referral of patients and discussion.
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