Literature DB >> 7794536

Transgenic models of HIV-1.

P E Klotman, J Rappaport, P Ray, J B Kopp, R Franks, L A Bruggeman, A L Notkins.   

Abstract

Transgenic technology has been very successful at providing insights into possible processes involved in HIV-induced pathogenesis. The availability of these small animal models for the study of HIV-related syndromes including KS, epidermal proliferative lesions, HIV-associated nephropathy, AIDS-related growth failure and cachexia may well facilitate the development of novel therapies for these complications. Other phenotypes created in mice, such as cataracts and hepatic cancer [59], may not have human analogies but may still provide insight into pathogenesis. Thus, transgenic models have already provided resources to study many manifestations of AIDS and others are likely to be developed. The optimal strategy for designing future transgenic animals, however, is less clear. No transgenic mouse model has been generated to date that will provide an avenue for vaccine development. This advance awaits the further discovery of the host factors that facilitate the virus replicative cycle in humans and a better understanding of these pathways in the mouse. For the development of molecular-based therapy, however, the currently available models may well be adequate to test molecular inhibitors of transcription [7,60,61] and post-transcriptional processing of viral mRNA [62]. Whether single or multigenic constructs under the control of the LTR are better or worse for this purpose is a debatable issue. Transgenic technology may yet make an additional contribution to the development of molecular therapy for AIDS. The best method of demonstrating that a gene therapeutic strategy is safe to administer to patients has not been determined. By introducing potentially therapeutic constructs into mice as transgenes, their safety can be assessed in many different cell types in vivo, analogous to toxicological testing in rodents for systemically administered drugs. Thus, transgenic technology has already provided insights into the pathogenesis of HIV-1. While it has not yet proven its utility for vaccine development, transgenic technology holds the promise of being an active participant in the development of both safe and effective gene therapy approaches for the treatment of AIDS.

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Year:  1995        PMID: 7794536

Source DB:  PubMed          Journal:  AIDS        ISSN: 0269-9370            Impact factor:   4.177


  11 in total

1.  Elevated levels of tumor necrosis factor alpha (TNF-alpha) in human immunodeficiency virus type 1-transgenic mice: prevention of death by antibody to TNF-alpha.

Authors:  Swapan K De; Krishnakumar Devadas; Abner Louis Notkins
Journal:  J Virol       Date:  2002-11       Impact factor: 5.103

2.  Inhibition of renin activity slows down the progression of HIV-associated nephropathy.

Authors:  Dileep Kumar; Andrei Plagov; Iti Yadav; Deepti D Torri; Swapna Sayeneni; Ankita Sagar; Partab Rai; Madhuri Adabala; Rivka Lederman; Nirupama Chandel; Guohua Ding; Ashwani Malhotra; Pravin C Singhal
Journal:  Am J Physiol Renal Physiol       Date:  2012-06-20

3.  Transgenic mice expressing human immunodeficiency virus type 1 in immune cells develop a severe AIDS-like disease.

Authors:  Z Hanna; D G Kay; M Cool; S Jothy; N Rebai; P Jolicoeur
Journal:  J Virol       Date:  1998-01       Impact factor: 5.103

Review 4.  New insights into HIV-1-primary skin disorders.

Authors:  Filiberto Cedeno-Laurent; Minerva Gómez-Flores; Nora Mendez; Jesús Ancer-Rodríguez; Joseph L Bryant; Anthony A Gaspari; Jose R Trujillo
Journal:  J Int AIDS Soc       Date:  2011-01-24       Impact factor: 5.396

Review 5.  Immunopathogenesis of oropharyngeal candidiasis in human immunodeficiency virus infection.

Authors:  Louis de Repentigny; Daniel Lewandowski; Paul Jolicoeur
Journal:  Clin Microbiol Rev       Date:  2004-10       Impact factor: 26.132

6.  Rabbit cells expressing human CD4 and human CCR5 are highly permissive for human immunodeficiency virus type 1 infection.

Authors:  R F Speck; M L Penn; J Wimmer; U Esser; B F Hague; T J Kindt; R E Atchison; M A Goldsmith
Journal:  J Virol       Date:  1998-07       Impact factor: 5.103

Review 7.  Neurotoxic profiles of HIV, psychostimulant drugs of abuse, and their concerted effect on the brain: current status of dopamine system vulnerability in NeuroAIDS.

Authors:  Mark J Ferris; Charles F Mactutus; Rosemarie M Booze
Journal:  Neurosci Biobehav Rev       Date:  2008-03-18       Impact factor: 8.989

8.  Rhesus macaques infected with macrophage-tropic simian immunodeficiency virus (SIVmacR71/17E) exhibit extensive focal segmental and global glomerulosclerosis.

Authors:  E B Stephens; C Tian; Z Li; O Narayan; V H Gattone
Journal:  J Virol       Date:  1998-11       Impact factor: 5.103

9.  Role of Apolipoprotein L1 in Human Parietal Epithelial Cell Transition.

Authors:  Vinod Kumar; Himanshu Vashistha; Xiqian Lan; Nirupama Chandel; Kamesh Ayasolla; Seyedeh Shadafarin Marashi Shoshtari; Rukhsana Aslam; Nitpriya Paliwal; Frank Abbruscato; Joanna Mikulak; Waldemar Popik; Mohamed G Atta; Praveen N Chander; Ashwani Malhotra; Catherine Meyer-Schwesinger; Karl Skorecki; Pravin C Singhal
Journal:  Am J Pathol       Date:  2018-09-08       Impact factor: 4.307

10.  Inflammatory papillomatous hyperplasia and epidermal necrosis in a transgenic rat for HIV-1.

Authors:  Filiberto Cedeno-Laurent; Joseph Bryant; Rita Fishelevich; Odell D Jones; April Deng; Maria L Eng; Anthony A Gaspari; J Roberto Trujillo
Journal:  J Dermatol Sci       Date:  2008-11-11       Impact factor: 4.563

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