Changing eye color by gene transduction
A person's iris color can lighten, such as from brown to lighter brown, green, hazel, or blue, by introducing a melanocyte-killing agent through the cornea of the person's eye and contacting the anterior surface of the iris with the agent at a dose sufficient to kill melanocytes in the iris stroma.
1. A method for changing a color of a subject's iris, comprising: introducing an effective dose of a gene vector directly into the anterior chamber of an eye of the subject, wherein the gene vector comprises is a recombinant adeno-associated virus comprising a suicide gene operably linked to a melanocyte-specific gene promoter, wherein the subject's iris is healthy; and wherein the introducing the effective dose of the gene vector is sufficient to kill melanocytes in a stroma of the healthy iris of the eye without inducing signs of inflammation in the anterior chamber, thereby changing the color of the iris.
2. The method of claim 1 , wherein the step of introducing is performed from outside the anterior chamber, through an opening in the cornea of the eye, into the anterior chamber.
3. The method of claim 1 , wherein the suicide gene is selected from the group consisting of (i) a herpes simplex virus thymidine kinase (HSVtk) gene; (ii) a cytosine deaminase gene; (iii) a nitroreductase gene; and (iv) a carboxypeptidase G2 gene.
4. The method of claim 1 , wherein the suicide gene comprises a herpes simplex virus thymidine kinase (HSVtk) gene.
5. The method of claim 4 , further comprising administering to the subject a nucleoside analog selected from the group consisting of ganciclovir, acyclovir, and valganciclovir.
6. The method of claim 1 , wherein the melanocyte-specific gene promoter is a promoter for tyrosinase (Tyr).
7. The method of claim 6 , wherein the suicide gene comprises a HSVtk gene operably linked to the melanocyte-specific gene promoter for Tyr.
8. The method of claim 1 , wherein the recombinant adeno-associated virus comprises an AAV1 or an AAV6 capsid protein.
9. The method of claim 1 , further comprising maintaining miosis of the pupil of the eye of the subject during the introducing and during a postoperative day after the introducing.
10. The method of claim 1 , wherein the effective dose of the gene vector is 5-50 μL of 1E10 to 1E13 vector genomes (vg)/ml.