Therapeutic applications of adeno-associated virus (AAV) gene transfer of HLA-G in the eye
The purpose of this paper is to review human leukocyte antigen G (HLA-G) in the eye, its
role in immune tolerance, and the potential therapeutic use of AAV gene transfer and …
role in immune tolerance, and the potential therapeutic use of AAV gene transfer and …
AAV vector-meditated expression of HLA-G reduces injury-induced corneal vascularization, immune cell infiltration, and fibrosis
ML Hirsch, LM Conatser, SM Smith, JH Salmon… - Scientific Reports, 2017 - nature.com
Over 1.5 million individuals suffer from cornea vascularization due to genetic and/or
environmental factors, compromising visual acuity and often resulting in blindness. Current …
environmental factors, compromising visual acuity and often resulting in blindness. Current …
AAV-mediated expression of HLA-G1/5 reduces severity of experimental autoimmune uveitis
Non-infectious uveitis (NIU) is an intractable, recurrent, and painful disease that is a
common cause of vision loss. Available treatments of NIU, such as the use of topical …
common cause of vision loss. Available treatments of NIU, such as the use of topical …
Ocular surface epithelial cells up-regulate HLA-G when expanded in vitro on amniotic membrane substrates
K Higa, S Shimmura, J Shimazaki, K Tsubota - Cornea, 2006 - journals.lww.com
Purpose: To study the modulation of immunoregulatory genes in ocular surface epithelial
cells cultured on amniotic membrane (AM). Methods: Microarray analysis was performed in …
cells cultured on amniotic membrane (AM). Methods: Microarray analysis was performed in …
Inducible Adeno-Associated Virus Vector–Delivered Transgene Expression in Corneal Endothelium
ML Tsai, SL Chen, PI Chou, LY Wen… - … & visual science, 2002 - iovs.arvojournals.org
purpose. To investigate whether recombinant adeno-associated virus (rAAV) vector–
mediated transgene expression is induced by inflammation in corneal endothelial cells in …
mediated transgene expression is induced by inflammation in corneal endothelial cells in …
Transduction, tropism, and biodistribution of AAV vectors in the lacrimal gland
EM Rocha, G Di Pasquale, PP Riveros… - … & visual science, 2011 - iovs.arvojournals.org
Purpose.: The lacrimal gland (LG) delivers defensive and metabolic factors to the ocular
surface. These functions may be disrupted in several diseases, and for most of them there is …
surface. These functions may be disrupted in several diseases, and for most of them there is …
Immunology of AAV-mediated gene transfer in the eye
K Willett, J Bennett - Frontiers in immunology, 2013 - frontiersin.org
The eye has been at the forefront of translational gene therapy largely owing to suitable
disease targets, anatomic accessibility, and well-studied immunologic privilege. These …
disease targets, anatomic accessibility, and well-studied immunologic privilege. These …
B-cell delivered gene transfer of human S-Ag-Ig fusion protein protects from experimental autoimmune uveitis
W Liang, Z Karabekian, Q Xu, AM Viley, DW Scott - Clinical Immunology, 2006 - Elsevier
Uveitis is an important autoimmune disease affecting an estimated 2.3 million Americans.
This disease is manifested by inflammation of the retina mediated by the infiltration of T …
This disease is manifested by inflammation of the retina mediated by the infiltration of T …
Adeno-associated and herpes simplex viruses as vectors for gene transfer to the corneal endothelium
T Hudde, SA Rayner, M De Alwis, AJ Thrasher, J Smith… - Cornea, 2000 - journals.lww.com
Purpose. We examined the efficacy and cytopathogenicity of adeno-associated (AAV) and
herpes simplex viruses (HSV) as vectors for gene transfer to corneal endothelial cells …
herpes simplex viruses (HSV) as vectors for gene transfer to corneal endothelial cells …
Preparation and administration of adeno-associated virus vectors for corneal gene delivery
Gene delivery approaches using adeno-associated virus (AAV) vectors are currently the
preferred method for human gene therapy applications and have demonstrated success in …
preferred method for human gene therapy applications and have demonstrated success in …