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Small Animal Models for Human Immunodeficiency Virus (HIV), Hepatitis B, and Tuberculosis: Proceedings of an NIAID Workshop.
Akkina, Ramesh; Barber, Daniel L; Bility, Moses T; Bissig, Karl-Dimiter; Burwitz, Benjamin J; Eichelberg, Katrin; Endsley, Janice J; Garcia, J Victor; Hafner, Richard; Karakousis, Petros C; Korba, Brent E; Koshy, Rajen; Lambros, Chris; Menne, Stephan; Nuermberger, Eric L; Ploss, Alexander; Podell, Brendan K; Poluektova, Larisa Y; Sanders-Beer, Brigitte E; Subbian, Selvakumar; Wahl, Angela.
Afiliação
  • Akkina R; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States.
  • Barber DL; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Bility MT; Department of Infectious Diseases and Microbiology, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
  • Bissig KD; Department of Pediatrics, Duke University, Durham, North Carolina, United States.
  • Burwitz BJ; Vaccine and Gene Therapy Institute, Oregon Health and Science University, Beaverton, Oregon, United States.
  • Eichelberg K; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Endsley JJ; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States.
  • Garcia JV; Division of Infectious Diseases, Center for AIDS Research, University of North Carolina at Chapel Hill, North Carolina, United States.
  • Hafner R; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Karakousis PC; Division of Infectious Diseases, Center for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
  • Korba BE; Department of Microbiology & Immunology, Georgetown University, Washington, DC, United States.
  • Koshy R; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Lambros C; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Menne S; Department of Microbiology & Immunology, Georgetown University, Washington, DC, United States.
  • Nuermberger EL; Division of Infectious Diseases, Center for Tuberculosis Research, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
  • Ploss A; Department of Molecular Biology, Princeton University, Princeton, New Jersey, United States.
  • Podell BK; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States.
  • Poluektova LY; Department of Pharmacology and Experimental Neuroscience and Translational Mouse Model Core Facility, University of Nebraska Medical Center, Omaha, Nebraska, United States.
  • Sanders-Beer BE; National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health, Bethesda, Maryland, United States.
  • Subbian S; The Public Health Research Institute Center of New Jersey Medical School, Rutgers University, Newark, New Jersey, United States.
  • Wahl A; Division of Infectious Diseases, Center for AIDS Research, University of North Carolina at Chapel Hill, North Carolina, United States.
Curr HIV Res ; 18(1): 19-28, 2020.
Article em En | MEDLINE | ID: mdl-31870268
ABSTRACT
The main advantage of animal models of infectious diseases over in vitro studies is the gain in the understanding of the complex dynamics between the immune system and the pathogen. While small animal models have practical advantages over large animal models, it is crucial to be aware of their limitations. Although the small animal model at least needs to be susceptible to the pathogen under study to obtain meaningful data, key elements of pathogenesis should also be reflected when compared to humans. Well-designed small animal models for HIV, hepatitis viruses and tuberculosis require, additionally, a thorough understanding of the similarities and differences in the immune responses between humans and small animals and should incorporate that knowledge into the goals of the study. To discuss these considerations, the NIAID hosted a workshop on 'Small Animal Models for HIV, Hepatitis B, and Tuberculosis' on May 30, 2019. Highlights of the workshop are outlined below.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose / Infecções por HIV / Vírus da Hepatite B / HIV-1 / Modelos Animais de Doenças / Hepatite B / Mycobacterium tuberculosis Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tuberculose / Infecções por HIV / Vírus da Hepatite B / HIV-1 / Modelos Animais de Doenças / Hepatite B / Mycobacterium tuberculosis Idioma: En Ano de publicação: 2020 Tipo de documento: Article