DOCSLIB.ORG

Treatment of Oculocutaneous/Ocular Albinism and for Increasing

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Treatment of Oculocutaneous/Ocular Albinism and for Increasing Treatment of Oculocutaneous/Ocular Albinism and for Increasing Pigmentation Summary (1024-character limit) The National Eye Institute's Ophthalmic Genetics and Visual Function Branch seeks interested commercial parties to co-develop the use of nitisinone (NTBC) for oculocutaneous albinism or as a treatment for increasing pigmentation in the eyes, hair and/or skin of patients. NIH Reference Number E-113-2010 Product Type Therapeutics Keywords Ocular disorders Albinism Pigmentation Nitisinone achromia, achromasia, achromatosis Collaboration Opportunity This invention is available for licensing and co-development. Contact Michael Salgaller, Ph.D. NCI - National Cancer Institute 240-276-5476 [email protected] Description of Technology Albinism (also called achromia, achromasia, or achromatosis) is a congenital disorder characterized by the complete or partial absence of pigment in the skin, hair and eyes due to absence or defect in any one of a number of proteins involved in the production of melanin. Certain forms of albinism are known to be due to mutations in tyrosine metabolism. In oculocutaneous albinism (OCA), pigment is lacking in the eyes, skin and hair. In ocular albinism, only the eyes lack pigment. Patients with albinism experience varying degrees of vision loss associated with foveal hypoplasia, nystagmus, photophobia and/or glare sensitivity, refractive errors, and abnormal decussation of ganglion cell axons at the optic chiasm. Current treatment options for vision problems caused by albinism are limited to correction of refractive NCI Technology Transfer Center https://techtransfer.cancer.gov/pdf/e-113-2010.pd f errors and amblyopia, low vision aids, and (in some cases) extraocular muscle surgery. Nitisinone (NTBC) is an FDA-approved drug used in the treatment of tyrosinemia, type 1. The drug blocks the normal degradation pathway of tyrosine thus allowing greater circulating plasma levels of tyrosine. NEI investigators identified administration of NTBC to subjects (e.g., mice or humans) with certain forms of albinism, can result in increased circulating tyrosine levels, an increase in tyrosinase activity, and, subsequently, increased pigmentation. Co-development research agreements with companies are sought to advance this treatment to humans. Potential Commercial Applications Nitisinone (NTBC) is an FDA-approved drug used in the treatment of tyrosinemia, type 1 Competitive Advantages Nitisinone (NTBC) is an FDA-approved drug used in the treatment of tyrosinemia, type 1 Inventor(s) Brian P. Brooks (NEI), William A Gahl (NHGRI), David R Adams (NHGRI) Development Stage Clinical Publications Adams DR et al. One-year pilot study on the effects of nitisinone on melanin in patients with OCA-1B. JCI Insight. 2019 Jan 24;4(2):e124387. doi: 10.1172/jci.insight.124387. Epub ahead of print. [PMID: 30674731] Brooks, B.P. Nitisinone for Type 1B Oculocutaneous Albinism. ClinicalTrials.gov Identifier: NCT01838655 Patent Status U.S. Patent Issued: U.S. Patent Number 8822540, Filed 06 Sep 2012, Issued 02 Sep 2014 Foreign Filed: Foreign Filed - Patent Application WO 02011106655 Foreign Issued: - Patent Number 2791245, Filed 25 Feb 2011, Issued 15 Jan 2019 Foreign Issued: EP - Patent Number 2538936, Filed 25 Feb 2011, Issued 24 Dec 2014 Foreign Issued: Australia - Patent Number 2011220475, Filed 25 Feb 2011, Issued 10 Jul 2014 Therapeutic Area Eye and Ear, Nose & Throat NCI Technology Transfer Center https://techtransfer.cancer.gov/pdf/e-113-2010.pd f.
Load more

Recommended publications
  • Melanocytes and Their Diseases
    Downloaded from http://perspectivesinmedicine.cshlp.org/ on October 2, 2021 - Published by Cold Spring Harbor Laboratory Press Melanocytes and Their Diseases Yuji Yamaguchi1 and Vincent J. Hearing2 1Medical, AbbVie GK, Mita, Tokyo 108-6302, Japan 2Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892 Correspondence: [email protected] Human melanocytes are distributed not only in the epidermis and in hair follicles but also in mucosa, cochlea (ear), iris (eye), and mesencephalon (brain) among other tissues. Melano- cytes, which are derived from the neural crest, are unique in that they produce eu-/pheo- melanin pigments in unique membrane-bound organelles termed melanosomes, which can be divided into four stages depending on their degree of maturation. Pigmentation production is determined by three distinct elements: enzymes involved in melanin synthesis, proteins required for melanosome structure, and proteins required for their trafficking and distribution. Many genes are involved in regulating pigmentation at various levels, and mutations in many of them cause pigmentary disorders, which can be classified into three types: hyperpigmen- tation (including melasma), hypopigmentation (including oculocutaneous albinism [OCA]), and mixed hyper-/hypopigmentation (including dyschromatosis symmetrica hereditaria). We briefly review vitiligo as a representative of an acquired hypopigmentation disorder. igments that determine human skin colors somes can be divided into four stages depend- Pinclude melanin, hemoglobin (red), hemo- ing on their degree of maturation. Early mela- siderin (brown), carotene (yellow), and bilin nosomes, especially stage I melanosomes, are (yellow). Among those, melanins play key roles similar to lysosomes whereas late melanosomes in determining human skin (and hair) pigmen- contain a structured matrix and highly dense tation.
    [Show full text]
  • EXTENDED CARRIER SCREENING Peace of Mind for Planned Pregnancies
    Focusing on Personalised Medicine EXTENDED CARRIER SCREENING Peace of Mind for Planned Pregnancies Extended carrier screening is an important tool for prospective parents to help them determine their risk of having a child affected with a heritable disease. In many cases, parents aren’t aware they are carriers and have no family history due to the rarity of some diseases in the general population. What is covered by the screening? Genomics For Life offers a comprehensive Extended Carrier Screening test, providing prospective parents with the information they require when planning their pregnancy. Extended Carrier Screening has been shown to detect carriers who would not have been considered candidates for traditional risk- based screening. With a simple mouth swab collection, we are able to test for over 419 genes associated with inherited diseases, including Fragile X Syndrome, Cystic Fibrosis and Spinal Muscular Atrophy. The assay has been developed in conjunction with clinical molecular geneticists, and includes genes listed in the NIH Genetic Test Registry. For a list of genes and disorders covered, please see the reverse of this brochure. If your gene of interest is not covered on our Extended Carrier Screening panel, please contact our friendly team to assist you in finding a gene test panel that suits your needs. Why have Extended Carrier Screening? Extended Carrier Screening prior to pregnancy enables couples to learn about their reproductive risk and consider a complete range of reproductive options, including whether or not to become pregnant, whether to use advanced reproductive technologies, such as preimplantation genetic diagnosis, or to use donor gametes.
    [Show full text]
  • Dermatologic Manifestations of Hermansky-Pudlak Syndrome in Patients with and Without a 16–Base Pair Duplication in the HPS1 Gene
    STUDY Dermatologic Manifestations of Hermansky-Pudlak Syndrome in Patients With and Without a 16–Base Pair Duplication in the HPS1 Gene Jorge Toro, MD; Maria Turner, MD; William A. Gahl, MD, PhD Background: Hermansky-Pudlak syndrome (HPS) con- without the duplication were non–Puerto Rican except sists of oculocutaneous albinism, a platelet storage pool de- 4 from central Puerto Rico. ficiency, and lysosomal accumulation of ceroid lipofuscin. Patients with HPS from northwest Puerto Rico are homozy- Results: Both patients homozygous for the 16-bp du- gous for a 16–base pair (bp) duplication in exon 15 of HPS1, plication and patients without the duplication dis- a gene on chromosome 10q23 known to cause the disorder. played skin color ranging from white to light brown. Pa- tients with the duplication, as well as those lacking the Objective: To determine the dermatologic findings of duplication, had hair color ranging from white to brown patients with HPS. and eye color ranging from blue to brown. New findings in both groups of patients with HPS were melanocytic Design: Survey of inpatients with HPS by physical ex- nevi with dysplastic features, acanthosis nigricans–like amination. lesions in the axilla and neck, and trichomegaly. Eighty percent of patients with the duplication exhibited fea- Setting: National Institutes of Health Clinical Center, tures of solar damage, including multiple freckles, stel- Bethesda, Md (a tertiary referral hospital). late lentigines, actinic keratoses, and, occasionally, basal cell or squamous cell carcinomas. Only 8% of patients Patients: Sixty-five patients aged 3 to 54 years were di- lacking the 16-bp duplication displayed these findings.
    [Show full text]
  • Preconception Carrier Screening
    Focusing on Personalised Medicine PRECONCEPTION CARRIER SCREENING Preconception carrier screening is an important tool for prospective parents to help them determine their risk of having a child affected with a heritable disease. In many cases, parents aren’t aware they are carriers and have no family history due to the rarity of some diseases in the general population. What is covered by the screening? Our Inherited Disease Panel tests over 300 genes associated with more than 700 unique commonly inherited diseases, including common forms of inherited deafness, blindness, heart disease, Parkinson’s disease, immunodeficiency, and various ataxias, anaemias, and treatable metabolic syndromes. The assay has been developed in conjunction with clinical molecular geneticists, and includeds genes listed in the NIH Genetic Test Registry. For a full list of genes and disorders covered, please see the reverse of this brochure. Why have Preconception Carrier Screening? Carrier screening prior to pregnancy enables couples to learn about their reproductive risk and consider a complete range of reproductive options, including whether or not to become pregnant, whether to use advanced reproductive technologies, such as preimplantation genetic diagnosis, or use donor gametes. Screening also allows couples to consider prenatal diagnosis and pregnancy management options in the event of an affected fetus. Whilst individually each disease tested is rare, around 25% of people will carry at least one abnormal mutation. These disorders are usually autosomal recessive, which means that a child must inherit a defective gene from each parent to have the disease. For autosomal recessive conditions, if a person is a carrier of the disease, they have one defective copy of the gene and one normal copy and typically don’t have any symptoms of the disease.
    [Show full text]
  • Oculocutaneous Albinism: an African Perspective
    Br Ir Orthopt J 2014; 11: 3–8 Oculocutaneous albinism: an African perspective GERALDINE R. McBRIDE1,2 MSc 1Orthoptic Department, Eye Clinic, University Hospital Galway, Galway, Ireland 2Kwale District Eye Centre, Kwale, Mombasa, Kenya Abstract behind OCA, and explore OCA in an African context in terms of the effects on the health and education of Aim: To describe the genetics behind oculocutaneous individuals with OCA. The outcome of this review will albinism (OCA), and explore OCA in an African be to provide useful advice to those with OCA and those context in terms of the effects on the health and working with or teaching students with OCA. education of individuals with OCA. Methods: A literature-based review was conducted using Pubmed. Searches were restricted to English- Genetics based publications, focusing on OCA in Africa. There are four different types of OCA, which result from Results: The genetics behind OCA and the effects of a mutation in one of several genes (Table 1).1,2,4 Each of OCA in terms of visual impairment and skin cancer these genes is chemically coded to produce proteins are explained along with a description of what low which are involved in the production of melanin. The vision services and low vision aids are available to mutation can result in the reduction of melanin pro- those with OCA in Africa. duction, or no melanin production.1 All four types of Conclusions: The review concludes with useful advice OCA are autosomal recessive. Therefore if both parents to those with OCA and those working with or are carriers of the mutated gene there is a 25% chance of teaching students with OCA.
    [Show full text]
  • Oculocutaneous Albinism, a Family Matter Summer Moon, DO,* Katherine Braunlich, DO,** Howard Lipkin, DO,*** Annette Lacasse, DO***
    Oculocutaneous Albinism, A Family Matter Summer Moon, DO,* Katherine Braunlich, DO,** Howard Lipkin, DO,*** Annette LaCasse, DO*** *Dermatology Resident, 3rd year, Botsford Hospital Dermatology Residency Program, Farmington Hills, MI **Traditional Rotating Intern, Largo Medical Center, Largo, FL ***Program Director, Botsford Hospital Dermatology Residency Program, Farmington Hills, MI Disclosures: None Correspondence: Katherine Braunlich, DO; [email protected] Abstract Oculocutaneous albinism (OCA) is a group of autosomal-recessive conditions characterized by mutations in melanin biosynthesis with resultant absence or reduction of melanin in the melanocytes. Herein, we present a rare case of two Caucasian sisters diagnosed with oculocutaneous albinism type 1 (OCA1). On physical exam, the sisters had nominal cutaneous evidence of OCA. This case highlights the difficulty of diagnosing oculocutaneous albinism in Caucasians. Additionally, we emphasize the uncommon underlying genetic mutations observed in individuals with oculocutaneous albinism. 2,5 Introduction people has one of the four types of albinism. of exon 4. Additionally, patient A was found to Oculocutaneous albinism (OCA) is a group of We present a rare case of sisters diagnosed with possess the c.21delC frameshift mutation in the autosomal-recessive conditions characterized by oculocutaneous albinism type 1, emphasizing the C10orf11 gene. Patient B was found to possess the mutations in melanin biosynthesis with resultant uncommon genetic mutations we observed in these same heterozygous mutation and deletion in the two individuals. absence or reduction of melanin in the melanocytes. Figure 1 Melanin-poor, pigment-poor melanocytes phenotypically present as hypopigmentation of the Case Report 1,2 Two Caucasian sisters were referred to our hair, skin, and eyes. dermatology clinic after receiving a diagnosis of There are four genes responsible for the four principal oculocutaneous albinism type 1.
    [Show full text]
  • Albinism: Modern Molecular Diagnosis
    British Journal of Ophthalmology 1998;82:189–195 189 Br J Ophthalmol: first published as 10.1136/bjo.82.2.189 on 1 February 1998. Downloaded from PERSPECTIVE Albinism: modern molecular diagnosis Susan M Carden, Raymond E Boissy, Pamela J Schoettker, William V Good Albinism is no longer a clinical diagnosis. The past cytes and into which melanin is confined. In the skin, the classification of albinism was predicated on phenotypic melanosome is later transferred from the melanocyte to the expression, but now molecular biology has defined the surrounding keratinocytes. The melanosome precursor condition more accurately. With recent advances in arises from the smooth endoplasmic reticulum. Tyrosinase molecular research, it is possible to diagnose many of the and other enzymes regulating melanin synthesis are various albinism conditions on the basis of genetic produced in the rough endoplasmic reticulum, matured in causation. This article seeks to review the current state of the Golgi apparatus, and translocated to the melanosome knowledge of albinism and associated disorders of hypo- where melanin biosynthesis occurs. pigmentation. Tyrosinase is a copper containing, monophenol, mono- The term albinism (L albus, white) encompasses geneti- oxygenase enzyme that has long been known to have a cally determined diseases that involve a disorder of the critical role in melanogenesis.5 It catalyses three reactions melanin system. Each condition of albinism is due to a in the melanin pathway. The rate limiting step is the genetic mutation on a diVerent chromosome. The cutane- hydroxylation of tyrosine into dihydroxyphenylalanine ous hypopigmentation in albinism ranges from complete (DOPA) by tyrosinase, but tyrosinase does not act alone.
    [Show full text]
  • A Neuroendocrine Theory for the Etiology of Vitiligo
    Cush ZM, J Med Stud Res 2018, 1: 007 DOI: 10.24966/MSR-5657/100007 HSOA Journal of Medicine: Study & Research Research Article of the skin, the melanocytes. The triggers, which range from sunburn A Neuroendocrine Theory for to mechanical trauma and chemical exposures, ultimately cause an autoimmune response those targets melanocytes, driving progressive the Etiology of Vitiligo skin depigmentation [3]. Zakiya M Cush* The New York Medical College, Valhalla, New York, USA Figure 1: Vitiligo is a condition in which the skin loses its pigment cells (melanocytes). This can result in discolored patches in different areas of the body, including the skin, hair, retina and mucous membranes [2]. Biochemistry of melanin formation Abstract According to published research, the adenylate cyclase signaling It has long been believed that vitiligo is an autoimmune disease. pathway, the stimulation of protein kinase C via DAG and the ty- And while there are many theories of this disease process, which rosine kinase activity mechanism (Figure 2) are responsible for the include cytotoxic and hereditary, there is another approach, which proliferation of melanocytes in mammals [4]. has yet to be considered. This paper will present a neuroendocrine hypothesis to why vitiligo occurs. With the understanding of the ty- rosinase enzyme, tyrosine kinase activity, and the Melanocytic Stim- ulating Hormone (MSH-α) and its effect on melanocyte production, an alternative approach to vitiligo should be considered, and it be- gins in the brain. Introduction What is vitiligo? Vitiligo is an acquired cutaneous disorder of pigmentation, with an incidence of 0.5% to 2% worldwide which, manifests as white mac- ules on the skin (Figure 1) and can cause significant psychological stress and stigmatization [1,2].
    [Show full text]
  • Social Discrimination Against People with Albinism
    Social discrimination against people with albinism * Mariah Nebre B.A. Candidate, Department of Sociology, California State University Stanislaus, 1 University Circle, Turlock, CA 95382 Received 16 April, 2018; accepted 15 May 2018 Abstract People with albinism have faced different forms of discrimination due to their genetic condition called oculocutaneous albinism. Oculocutaneous albinism, also known as OCA, is a genetic condition that results in people with low skin pigmentation and melanin levels in their hair, skin, and eyes to varying degrees. People who are afflicted with OCA have a high percentage of visual impairment and life- threating sensitivity to the sun. Affected individuals also face negative outcomes of social, cultural, and economic prejudice because of the lack of color that their skin provides. People with albinism are shunned by the rest of their community and are at a high risk of being killed because of their unique physical features. The most common location where people with albinism are discriminated against is in Africa. In this exploratory study, research was conducted by interviewing four people with albinism to get an understanding of the social discrimination they faced. In these in-depth interviews, the focus was on the social aspect of their past and present lives and how they go about addressing any positive and/or negative outcomes they face in society because of their genetic condition. In addition, undergraduate students were surveyed from different fields of study to get an understanding of how much knowledge students have about albinism and its social aspects. Some of the majors surveyed include: biology, sociology, psychology, and liberal studies.
    [Show full text]
  • Nitisinone-Induced Keratopathy in Alkaptonuria Disease: a Case
    DOI: 10.7860/JCDR/2018/35741.11629 Case Report Nitisinone-Induced Keratopathy in Alkaptonuria Disease: A Case Ophthalmology Section Report and Literature Review KHALID MOUSA AL ZUBI1, MOHAMMED SALEM ALSBOU2, MAHMOUD HUSSEIN ALKHASAWNEH3, HANI MOSLEH AL-SHAGAHIN4 ABSTRACT We report a case of nitisinone-induced keratopathy in a 52-year-old male patient with Alkaptonuria (AKU) disease in Jordan. The patient presented with slight drop of left eye vision for the last four weeks, associated with a foreign body sensation in his left eye. On examination, it was found that his left eye vision was reduced to 6/12 and there were left dendrite-like corneal opacities in the left eye. He was given 10 mg of nitisinone per day, two years before his visual complaint. Three months following discontinuation of nitisinone, his visual acuity and corneal opacities disappeared completely. This is the fifth reported case of nitisinone-induced keratopathy, due to secondary tyrosinaemia in alkaptonuria. Keywords: Pseudodendritic keratitis, Richner–Hanhart syndrome, Tyrosinaemia CASE REPORT in both eyes, and his corneal opacities were completely resolved A 52-year-old male patient, known case of alkaptonuria, presenting [Table/Fig-2]. Serum tyrosine level was also within normal limits at to the Eye Center with a chief complaint of blurred vision and foreign 76.6 µmol/L. body sensation in the left eye for the last four weeks from the date of presentation. The patient had history of severe low back pain, morning stiffness, and pain in his both knees and hips 17 years prior to the present complaint. Clinical examination revealed a bluish-grey pigmentation of both ears.
    [Show full text]
  • TYR Gene Tyrosinase
    TYR gene tyrosinase Normal Function The TYR gene provides instructions for making an enzyme called tyrosinase. This enzyme is located in melanocytes, which are specialized cells that produce a pigment called melanin. Melanin is the substance that gives skin, hair, and eyes their color. Melanin is also found in the light-sensitive tissue at the back of the eye (the retina), where it plays a role in normal vision. Tyrosinase is responsible for the first step in melanin production. It converts a protein building block (amino acid) called tyrosine to another compound called dopaquinone. A series of additional chemical reactions convert dopaquinone to melanin in the skin, hair follicles, the colored part of the eye (the iris), and the retina. Health Conditions Related to Genetic Changes Oculocutaneous albinism More than 100 mutations in the TYR gene have been identified in people with oculocutaneous albinism type 1. These mutations disrupt the normal production of melanin, which reduces coloring of the hair, skin, and eyes and causes problems with vision. Most TYR mutations eliminate the activity of tyrosinase, preventing melanocytes from producing any melanin throughout life. These mutations cause a form of oculocutaneous albinism called type 1A (OCA1A). People with this form of albinism have white hair, light-colored eyes, and very pale skin that does not tan. Other mutations in the TYR gene reduce but do not eliminate tyrosinase activity. These mutations, which allow some melanin to be produced, cause oculocutaneous albinism type 1B (OCA1B). People with type 1B are also born with white hair, light-colored eyes, and pale skin, but hair and eye color often darken over time and skin may tan.
    [Show full text]
  • Repositioning of Nitisinone to Treat Oculocutaneous Albinism
    Informed reasoning: repositioning of nitisinone to treat oculocutaneous albinism Prashiela Manga, Seth J. Orlow J Clin Invest. 2011;121(10):3828-3831. https://doi.org/10.1172/JCI59763. Commentary Oculocutaneous albinism (OCA) is a group of genetic disorders characterized by hypopigmentation of the skin, hair, and eyes. Affected individuals experience reduced visual acuity and substantially increased skin cancer risk. There are four major types of OCA (OCA1–OCA4) that result from disruption in production of melanin from tyrosine. Current treatment options for individuals with OCA are limited to attempts to correct visual problems and counseling to promote use of sun protective measures. However, Onojafe et al., reporting in this issue of the JCI, provide hope for a new treatment approach for OCA, as they demonstrate that treating mice that model OCA-1b with nitisinone, which is FDA approved for treating hereditary tyrosinemia type 1, elevates plasma tyrosine levels, and increases eye and hair pigmentation. Find the latest version: https://jci.me/59763/pdf commentaries Informed reasoning: repositioning of nitisinone to treat oculocutaneous albinism Prashiela Manga and Seth J. Orlow Ronald O. Perelman Department of Dermatology and Department of Cell Biology, New York University School of Medicine, New York, New York, USA. Oculocutaneous albinism (OCA) is a group of genetic disorders characterized Melanin synthesis and its disruption by hypopigmentation of the skin, hair, and eyes. Affected individuals experi- in OCA ence reduced visual acuity and substantially increased skin cancer risk. There Tyrosinase, a type I membrane protein, are four major types of OCA (OCA1–OCA4) that result from disruption in catalyzes the first and rate-limiting reac- production of melanin from tyrosine.
    [Show full text]