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1.
Hum Gene Ther ; 34(7-8): 273-288, 2023 04.
Article in English | MEDLINE | ID: mdl-36927149

ABSTRACT

The liver is a prime target for in vivo gene therapies using recombinant adeno-associated viral vectors. Multiple clinical trials have been undertaken for this target in the past 15 years; however, we are still to see market approval of the first liver-targeted adeno-associated virus (AAV)-based gene therapy. Inefficient expression of the therapeutic transgene, vector-induced liver toxicity and capsid, and/or transgene-mediated immune responses reported at high vector doses are the main challenges to date. One of the contributing factors to the insufficient clinical outcomes, despite highly encouraging preclinical data, is the lack of robust, biologically and clinically predictive preclinical models. To this end, this study reports findings of a functional evaluation of 6 AAV vectors in 12 preclinical models of the human liver, with the aim to uncover which combination of models is the most relevant for the identification of AAV capsid variant for safe and efficient transgene delivery to primary human hepatocytes. The results, generated by studies in models ranging from immortalized cells, iPSC-derived and primary hepatocytes, and primary human hepatic organoids to in vivo models, increased our understanding of the strengths and weaknesses of each system. This should allow the development of novel gene therapies targeting the human liver.


Subject(s)
Dependovirus , Liver , Humans , Dependovirus/genetics , Liver/metabolism , Genetic Therapy/methods , Hepatocytes/metabolism , Capsid Proteins/metabolism , Tropism , Genetic Vectors/genetics
2.
Appl Immunohistochem Mol Morphol ; 29(2): 158-162, 2021 02 01.
Article in English | MEDLINE | ID: mdl-32858540

ABSTRACT

Formalin-fixed paraffin-embedded (FFPE) tissues are an important source for investigation of dengue virus (DENV) infection, particularly when blood or fresh frozen (FF) samples are unavailable. Histopathologic features and immunohistochemistry may have poor sensitivity and serotype determination is not always possible. Viral RNA genome detection tests are faster and considered the most sensitive technique for this kind of analysis, however, the use of molecular methods applied to FFPE tissues is still limited. The authors applied a single-step multiplex reverse transcription-quantitative polymerase chain reaction (RT-qPCR) for the investigation of DENV infection and typing to FFPE samples of 32 fatal cases received during the 2019 outbreak that occurred in São Paulo state, Brazil. The authors compared the results with those obtained using FF tissues. Of the 24 cases with both FF and FFPE samples, 22 (91.67%) of the FF and 19 (76.20%) of the FFPE specimens were positive. Two cases (8.33%) tested negative in both types of samples. All 8 cases with only FFPE samples available were positive. The accuracy (87.5%) of the RT-qPCR for DENV in FFPE samples were satisfactory. Although the cycle quantification (Cq) values were significantly higher in these materials (P<0.0001, Wilcoxon signed-rank test) when compared with FF tissues, Spearman's rank coefficient indicated a good correlation between the Cq values from both sample types (P=0.0063; rho=0.576). RT-qPCR applied to FFPE samples improved detection of DENV in fatal cases and represents a useful tool for diagnosis and epidemiologic studies.


Subject(s)
Dengue Virus/genetics , Dengue , Disease Outbreaks , Multiplex Polymerase Chain Reaction , Paraffin Embedding , Real-Time Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Brazil/epidemiology , Cross-Sectional Studies , Dengue/diagnosis , Dengue/genetics , Dengue/mortality , Dengue/pathology , Female , Humans , Male
3.
Appl Immunohistochem Mol Morphol ; 28(6): 484-487, 2020 07.
Article in English | MEDLINE | ID: mdl-31633490

ABSTRACT

The cell block (CB) technique has allowed easy obtainment of samples such as cellular and culture suspensions, to perform specific molecular tests such as immunohistochemistry and in situ hybridization. It has been improved along time, accuracy, and quality of the diagnoses, however, the cost of a commercial gel matrix for the preparation of CB is high and not suitable depending on the situation. The objective of this study is to test agarose as an alternative to the commercial gel matrix in the preparation of Aspergillus fumigatus' CB.


Subject(s)
Aspergillus fumigatus/isolation & purification , Aspergillus fumigatus/metabolism , Cell Culture Techniques/methods , Communicable Diseases/diagnosis , Aspergillus fumigatus/genetics , Communicable Diseases/microbiology , Humans , Immunohistochemistry , In Situ Hybridization , Polymerase Chain Reaction , RNA, Ribosomal, 18S/genetics
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