Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene
Inherited retinal dystrophies (IRD) is an extensive group of genetically heterogeneous diseases with significant clinical polymorphism. With the development of gene therapy, a new era in the treatment of hereditary human diseases has opened. To date, clinical studies of a number of gene medication...
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
Real Time Ltd
2021-09-01
|
| Series: | Российский офтальмологический журнал |
| Subjects: | |
| Online Access: | https://roj.igb.ru/jour/article/view/722 |
| _version_ | 1797878329098895360 |
|---|---|
| author | V. V. Neroev L. A. Katargina V. V. Kadyshev I. V. Zolnikova S. I. Kutsev |
| author_facet | V. V. Neroev L. A. Katargina V. V. Kadyshev I. V. Zolnikova S. I. Kutsev |
| author_sort | V. V. Neroev |
| collection | DOAJ |
| description | Inherited retinal dystrophies (IRD) is an extensive group of genetically heterogeneous diseases with significant clinical polymorphism. With the development of gene therapy, a new era in the treatment of hereditary human diseases has opened. To date, clinical studies of a number of gene medications are performed the world over, including those intended for the treatment of hereditary eye diseases (Leber congenital amaurosis (LCA), retinitis pigmentosa, achromatopsia, Stargardt's disease, choroideremia, etc.). The varieties of two former conditions, specifically LCA type 2 and retinitis pigmentosa (RP) type 20 with biallelic mutations in the RPE65 gene belong to IRD. Epidemiological studies indicate the rarity of these diseases, which explains why IRD caused by biallelic mutations in the RPE65 gene are included into the list of rare (orphan) diseases of the Russian Ministry of Health. For these IRDs, a gene replacement therapy has been developed: voretigen neparvovek, which must only be applied once. Currently, the Medical Genetic Research Center and Helmholtz National Medical Research Center of Eye Diseases have identified a group of patients who meet the criteria for genetic therapy. In 2021, а specialized gene therapy center has been established at the Helmholtz Research Center, which was certified by the Ministry of Health. A group of leading experts in the field of inherited retinal diseases and medical genetics developed and approved at professional workshops a number of measures that promote the introduction into clinical practice of the voretigen neparvovek as a gene replacement therapy for the treatment of RPE65-related IRD in the Russian Federation. |
| first_indexed | 2024-04-10T02:30:56Z |
| format | Article |
| id | doaj.art-ec6b24b014894703822a2852f186d87f |
| institution | Directory Open Access Journal |
| issn | 2072-0076 2587-5760 |
| language | Russian |
| last_indexed | 2024-04-10T02:30:56Z |
| publishDate | 2021-09-01 |
| publisher | Real Time Ltd |
| record_format | Article |
| series | Российский офтальмологический журнал |
| spelling | doaj.art-ec6b24b014894703822a2852f186d87f2023-03-13T07:54:31ZrusReal Time LtdРоссийский офтальмологический журнал2072-00762587-57602021-09-01143788210.21516/2072-0076-2021-14-3-78-82377Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 geneV. V. Neroev0L. A. Katargina1V. V. Kadyshev2I. V. Zolnikova3S. I. Kutsev4ФГБУ «НМИЦ глазных болезней им. Гельмгольца» Минздрава России; ФГБОУ ВО «Московский государственный медико-стоматологический университет им. А.И. Евдокимова» Минздрава РоссииФГБУ «НМИЦ глазных болезней им. Гельмгольца» Минздрава РоссииФГБНУ «Медико-генетический научный центр им. академика Н.П. Бочкова»ФГБУ «НМИЦ глазных болезней им. Гельмгольца» Минздрава России; ФГБНУ «Медико-генетический научный центр им. академика Н.П. Бочкова»ФГБНУ «Медико-генетический научный центр им. академика Н.П. Бочкова»Inherited retinal dystrophies (IRD) is an extensive group of genetically heterogeneous diseases with significant clinical polymorphism. With the development of gene therapy, a new era in the treatment of hereditary human diseases has opened. To date, clinical studies of a number of gene medications are performed the world over, including those intended for the treatment of hereditary eye diseases (Leber congenital amaurosis (LCA), retinitis pigmentosa, achromatopsia, Stargardt's disease, choroideremia, etc.). The varieties of two former conditions, specifically LCA type 2 and retinitis pigmentosa (RP) type 20 with biallelic mutations in the RPE65 gene belong to IRD. Epidemiological studies indicate the rarity of these diseases, which explains why IRD caused by biallelic mutations in the RPE65 gene are included into the list of rare (orphan) diseases of the Russian Ministry of Health. For these IRDs, a gene replacement therapy has been developed: voretigen neparvovek, which must only be applied once. Currently, the Medical Genetic Research Center and Helmholtz National Medical Research Center of Eye Diseases have identified a group of patients who meet the criteria for genetic therapy. In 2021, а specialized gene therapy center has been established at the Helmholtz Research Center, which was certified by the Ministry of Health. A group of leading experts in the field of inherited retinal diseases and medical genetics developed and approved at professional workshops a number of measures that promote the introduction into clinical practice of the voretigen neparvovek as a gene replacement therapy for the treatment of RPE65-related IRD in the Russian Federation.https://roj.igb.ru/jour/article/view/722амавроз леберагенная терапияпигментный ретинитгенетикагетерогенностьrpe65воретиген непарвовек |
| spellingShingle | V. V. Neroev L. A. Katargina V. V. Kadyshev I. V. Zolnikova S. I. Kutsev Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene Российский офтальмологический журнал амавроз лебера генная терапия пигментный ретинит генетика гетерогенность rpe65 воретиген непарвовек |
| title | Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene |
| title_full | Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene |
| title_fullStr | Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene |
| title_full_unstemmed | Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene |
| title_short | Prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the RPE65 gene |
| title_sort | prospects for the diagnosis and gene therapy of inherited retinal dystrophies caused by biallelic mutations in the rpe65 gene |
| topic | амавроз лебера генная терапия пигментный ретинит генетика гетерогенность rpe65 воретиген непарвовек |
| url | https://roj.igb.ru/jour/article/view/722 |
| work_keys_str_mv | AT vvneroev prospectsforthediagnosisandgenetherapyofinheritedretinaldystrophiescausedbybiallelicmutationsintherpe65gene AT lakatargina prospectsforthediagnosisandgenetherapyofinheritedretinaldystrophiescausedbybiallelicmutationsintherpe65gene AT vvkadyshev prospectsforthediagnosisandgenetherapyofinheritedretinaldystrophiescausedbybiallelicmutationsintherpe65gene AT ivzolnikova prospectsforthediagnosisandgenetherapyofinheritedretinaldystrophiescausedbybiallelicmutationsintherpe65gene AT sikutsev prospectsforthediagnosisandgenetherapyofinheritedretinaldystrophiescausedbybiallelicmutationsintherpe65gene |