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Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cells

Abstract:
Funder: NIHR Oxford Biomedical Research CentreDry age-related macular degeneration (AMD) is characterised by loss of central vision and currently has no approved medical treatment. Dysregulation of the complement system is thought to play an important role in disease pathology and supplementation of Complement Factor I (CFI), a key regulator of the complement system, has the potential to provide a treatment option for AMD. In this study, we demonstrate the generation of AAV constructs carrying the human CFI sequence and expression of CFI in cell lines and in the retina of C57BL/6 J mice. Four codon optimised constructs were compared to the most common human CFI sequence. All constructs expressed CFI protein; however, most codon optimised sequences resulted in significantly reduced CFI secretion compared to the non-optimised CFI sequence. In vivo expression analysis showed that CFI was predominantly expressed in the RPE and photoreceptors. Secreted protein in vitreous humour was demonstrated to be functionally active. The findings presented here have led to the formulation of an AAV-vectored gene therapy product currently being tested in a first-in-human clinical trial in subjects with geographic atrophy secondary to dry AMD (NCT03846193)
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41434-021-00239-9

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Role:
Author
ORCID:
0000-0001-5904-0961
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-2941-4464
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-0662-1073
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Role:
Author
ORCID:
0000-0002-8306-5250


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Funder identifier:
10.13039/501100013373


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
Gene Therapy More from this journal
Volume:
28
Issue:
5
Pages:
265-276
Publication date:
2021-03-10
DOI:
EISSN:
1476-5462
ISSN:
0969-7128


Language:
English
Keywords:
Pubs id:
1169993
Local pid:
pubs:1169993
Source identifiers:
W3133600954
Deposit date:
2026-02-14
ARK identifier:
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