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1.
Gene Ther ; 20(8): 824-33, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23344065

ABSTRACT

Usher 1 patients are born profoundly deaf and then develop retinal degeneration. Thus they are readily identified before the onset of retinal degeneration, making gene therapy a viable strategy to prevent their blindness. Here, we have investigated the use of adeno-associated viruses (AAVs) for the delivery of the Usher 1B gene, MYO7A, to retinal cells in cell culture and in Myo7a-null mice. MYO7A cDNA, under control of a smCBA promoter, was packaged in single AAV2 and AAV5 vectors and as two overlapping halves in dual AAV2 vectors. The 7.9-kb smCBA-MYO7A exceeds the capacity of an AAV vector; packaging of such oversized constructs into single AAV vectors may involve fragmentation of the gene. Nevertheless, the AAV2 and AAV5 single vector preparations successfully transduced photoreceptor and retinal pigment epithelium cells, resulting in functional, full-length MYO7A protein and correction of mutant phenotypes, suggesting successful homologous recombination of gene fragments. With discrete, conventional-sized dual AAV2 vectors, full-length MYO7A was detected, but the level of protein expression was variable, and only a minority of cells showed phenotype correction. Our results show that MYO7A therapy with AAV2 or AAV5 single vectors is efficacious; however, the dual AAV2 approach proved to be less effective.


Subject(s)
Genetic Therapy , Myosins/genetics , Retinal Degeneration/genetics , Retinal Degeneration/therapy , Usher Syndromes/therapy , Animals , DNA, Complementary , Dependovirus , Gene Expression , Gene Transfer Techniques , Green Fluorescent Proteins/genetics , Humans , Mice , Myosin VIIa , Myosins/metabolism , Retina/pathology , Retinal Degeneration/pathology , Usher Syndromes/genetics , Usher Syndromes/pathology
2.
Arq Bras Cardiol ; 73(3): 281-90, 1999 Sep.
Article in English, Portuguese | MEDLINE | ID: mdl-10752167

ABSTRACT

OBJECTIVE: To evaluate the cardiac abnormalities and their evolution during the course of the acquired immunodeficiency syndrome, as well as to correlate clinical and pathological data. METHODS: Twenty-one patients, admitted to the hospital with the diagnosis of acquired immunodeficiency syndrome, were prospectively studied and followed until their death. Age ranged from 19 to 42 years (17 males). ECG and echocardiogram were also obtained every six months. After death, macro- and microscopic examinations were also performed. RESULTS: The most frequent causes of referral to the hospital were: diarrhea or repeated pneumonias, tuberculosis, toxoplasmosis or Kaposi sarcoma. The most frequent findings were acute or chronic pericarditis (42%) and dilated cardiomyopathy (19%). Four patients died of cardiac problems: infective endocarditis, pericarditis with pericardial effusion, bacterial myocarditis and infection by Toxoplasma gondii. CONCLUSION: Severe cardiac abnormalities were the cause of death in some patients. In the majority of the patients, a good correlation existed between clinical and anatomical-pathological data. Cardiac evaluation was important to detect early manifestations and treat them accordingly, even in asymptomatic patients.


Subject(s)
Acquired Immunodeficiency Syndrome/complications , Heart Diseases/etiology , Adult , Electrocardiography , Female , Heart Diseases/pathology , Heart Failure/etiology , Heart Failure/mortality , Heart Failure/pathology , Humans , Male , Prospective Studies
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