A Cinnamon-Derived Procyanidin Compound Displays Anti-HIV-1 Activity by Blocking Heparan Sulfate- and Co-Receptor- Binding Sites on gp120 and Reverses T Cell Exhaustion via Impeding Tim-3 and PD-1 Upregulation. [electronic resource]
Producer: 20170615Description: e0165386 p. digitalISSN:- 1932-6203
- Anti-HIV Agents -- chemistry
- Biflavonoids -- chemistry
- Binding Sites
- CD4 Antigens -- metabolism
- CD4-Positive T-Lymphocytes -- drug effects
- CD8-Positive T-Lymphocytes -- drug effects
- Catechin -- chemistry
- Cinnamomum zeylanicum -- chemistry
- HIV Envelope Protein gp120 -- metabolism
- Heparitin Sulfate -- metabolism
- Hepatitis A Virus Cellular Receptor 2 -- metabolism
- Humans
- Proanthocyanidins -- chemistry
- Programmed Cell Death 1 Receptor -- metabolism
- T-Lymphocytes -- drug effects
- Up-Regulation -- drug effects
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Publication Type: Journal Article
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