>>9821472
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Dr Fauci continued
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https://pubmed.ncbi.nlm.nih.gov/22820788/
https://archive.is/wip/x6r2o
JAMA. 2012 Jul 25;
308(4):353-61. doi: 10.1001/jama.2012.6936.
Effects of Hydroxychloroquine on Immune Activation and Disease Progression Among HIV-infected Patients Not Receiving Antiretroviral Therapy: A Randomized Controlled Trial
Intervention: Hydroxychloroquine, 400 mg, or matching placebo once daily for 48 weeks.
Among HIV-infected patients not taking antiretroviral therapy, the use of hydroxychloroquine compared with placebo did not reduce CD8 cell activation but did result in a greater decline in CD4 cell count and increased viral replication.
linked to from: http://www.isrctn.com/ISRCTN30019040
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https://www.sciencedirect.com/science/article/abs/pii/0149291895800395
https://archive.is/wip/o7dvv
Clinical Therapeutics
Volume 17, Issue 4, July–August 1995, Pages 622-636
Hydroxychloroquine treatment of patients with human immunodeficiency virus type 1
Hydroxychloroquine (HCQ), an antimalarial agent used to treat patients with autoimmune diseases, has been shown to suppress human immunodeficiency virus type 1 (HIV-1) replication in vitro in T cells and monocytes
HCQ thus may be useful in the treatment of patients with HIV-1 infection.
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https://www.aidsmap.com/news/jul-2016/hiv-will-only-be-cured-combinations-too-conference-delegates-hear
https://archive.is/dIDw5
Dr Anthony Fauci, head of the US National Institute of Allergies and Infectious Diseases, told delegates that HIV cure research was roughly at the stage HIV treatment was in 1990; as with the first HIV drug AZT (zidovudine), it was becoming clear that single agents or strategies might only have the most limited effect, and dual combinations were starting to show somewhat more promise.
Even combinations don’t work if they lack a crucial step in the sequence of events that would need to happen for HIV-infected cells to be purged from the body. The Towards a Cure workshop, and the main conference, heard about disappointing results from an experimental regimen consisting of three drugs; the immune modulator drug vorinostat, chosen because it can ‘wake up’ the long-lived reservoir cells in which HIV lies hidden; the anti-malaria drug hydroxychloroquine, chosen to contain the immune stimulant effects of vorinostat and prevent runaway HIV infection; and the entry inhibitor maraviroc, chosen because it has the potential to stop HIV spreading to new cells once the reservoir cells are woken up.
This ‘VHM’ combination was given to ten people with HIV who had been diagnosed within two to four weeks of infection, treated immediately with antiretroviral therapy (ART) and kept on ART for at least two years. It was hoped that the ‘kick’ given by this regimen would induce the body’s immune system to spontaneously eliminate the HIV-infected cells that had now become visible to it, or would convert naturally to a short-lived type that would die.
Presenter Jintanat Ananworanich told the workshop that the reason VHM did not work was probably because, as other ‘kick and kill’ studies had found, that it was not enough to flush the HIV reservoir cells out of hiding. It turned out that the body’s natural immune processes did not then kill these calls and that a ‘kill’ component or toxin that actively targeted the reawakened reservoir cells would have to be added.