4.4 Article

HIV-1 and drug abuse comorbidity: Lessons learned from the animal models of NeuroHIV

期刊

NEUROSCIENCE LETTERS
卷 754, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2021.135863

关键词

HIV; Drug abuse; HAND; Animal models; SIV; Rhesus macaques

资金

  1. NIH NIDA [DA050545, DA044586, DA047156, DA043138, DA052266]
  2. CHAIN (Chronic HIV infection and Aging in NeuroAIDS) Center grant [MH062261]
  3. NCSAR (Nebraska Center for Substance Abuse Research)

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Various research studies have explored the impact of drug abuse on HIV infection and disease progression, highlighting the impairments in host immunological and non-immunological pathways. Despite efforts to develop rodent models of HAND, none can fully replicate the complex pathophysiology of the syndrome, but they do model some unique aspects of HAND.
Various research studies that have investigated the association between HIV infection and addiction underpin the role of various drugs of abuse in impairing immunological and non-immunological pathways of the host system, ultimately leading to augmentation of HIV infection and disease progression. These studies have included both in vitro and in vivo animal models wherein investigators have assessed the effects of various drugs on several disease parameters to decipher the impact of drugs on both HIV infection and progression of HIV-associated neurocognitive disorders (HAND). However, given the inherent limitations in the existing animal models of HAND, these investigations only recapitulated specific aspects of the disease but not the complex human syndrome. Despite the inability of HIV to infect rodents over the last 30 years, multiple strategies have been employed to develop several rodent models of HAND. While none of these models can accurately mimic the overall pathophysiology of HAND, they serve the purpose of modeling some unique aspects of HAND. This review provides an overview of various animal models used in the field and a careful evaluation of methodological strengths and limitations inherent in both the model systems and study designs to understand better how the various animal models complement one another.

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