Ciliary neurotrophic factor (CNTF) for human retinal degeneration: Phase I trial of CNTF delivered by encapsulated cell intraocular implants

Paul A. Sieving, Rafael C. Caruso, Weng Tao, Hanna R. Coleman, Darby J. S. Thompson, K. R. Fullmer, Ronald A. Bush

Proceedings of the National Academy of Sciences · 2006 · 592 citations · 44 references

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TL;DR

Neurotrophic factors can slow photoreceptor degeneration in animal models of retinitis pigmentosa, and encapsulated cell implants for delivering such proteins may be applicable beyond genetic mutation–driven diseases. Here we report a human clinical trial of a neurotrophic factor for retinal neurodegeneration. In this Phase I safety trial, human ciliary neurotrophic factor was delivered by genetically modified cells encapsulated in semipermeable capsules surgically implanted into the vitreous, with ten participants receiving implants in one eye. The implants remained viable with therapeutic CNTF output, and among seven eyes with measurable acuity, three showed sustained 10–15‑letter gains while a transient acuity loss from choroidal detachment resolved, indicating CNTF is safe for the human retina even with severely compromised photoreceptors.

Abstract

Neurotrophic factors are agents with a promising ability to retard progression of neurodegenerative diseases and are effective in slowing photoreceptor degeneration in animal models of retinitis pigmentosa. Here we report a human clinical trial of a neurotrophic factor for retinal neurodegeneration. In this Phase I safety trial, human ciliary neurotrophic factor (CNTF) was delivered by cells transfected with the human CNTF gene and sequestered within capsules that were surgically implanted into the vitreous of the eye. The outer membrane of the encapsulated cell implant is semipermeable to allow CNTF to reach the retina. Ten participants received CNTF implants in one eye. When the implants were removed after 6 months, they contained viable cells with minimal cell loss and gave CNTF output at levels previously shown to be therapeutic for retinal degeneration in rcd1 dogs. Although the trial was not powered to form a judgment as to clinical efficacy, of seven eyes for which visual acuity could be tracked by conventional reading charts, three eyes reached and maintained improved acuities of 10–15 letters, equivalent to two- to three-line improvement on standard Snellen acuity charts. A surgically related choroidal detachment in one eye resulted in a transient acuity decrease that resolved with conservative management. This Phase I trial indicated that CNTF is safe for the human retina even with severely compromised photoreceptors. The approach to delivering therapeutic proteins to degenerating retinas using encapsulated cell implants may have application beyond disease caused by genetic mutations.

References

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