- Alovudine
- ALVAC 1433
- AMD070
- AV-1101
- AVX754
- Azodicarbonamide (ADA)
- BMS-488043
- Brecanavir
- Buspirone hydrochloride (Buspar)
- Calanolide A
- Calcium spirulan
- CD4-based therapies
- Cell Genesys gene therapy
- Cimetidine (Dyspamet / Tagamet)
- Colony stimulating factors
- Curcumin
- Dapivirine
- Dextran sulphate
- Dinitrochlorobenzene (DNCB)
- Elvucitabine
- Etravirine
- Extracorporeal photopheresis
- FP-21399
- GPG-NH2
- GS 9137
- GW695634
- GW8248
- HEPT derivatives
- HGP-30
- HGTV43
- Hydroxycarbamide (Hydrea)
- Hyperthermia
- Interferon gamma-1b (Immukin)
- Interleukin-12
- Interleukin-16
- Intravenous immunoglobulin
- Iscador
- Isoprinosine
- JE-2147
- Lentinan
- Malariotherapy
- Maraviroc
- MIV 150
- MK-0518
- MVA-BN-Nef vaccine
- Mycophenolate mofetil (CellCept)
- Ozone
- P-1946
- p24.VLP
- PA-457
- Passive immunotherapy
- Phosphazid
- PN355
- PRO 2000
- PRO 542
- pTHr.HIVA
- Racivir
- Remune
- S-1360
- SJ-3366
- SP1093V
- SPV-30
- Stampidine
- T-1249
- Tat toxoid vaccine
- Thymic peptides
- TMC278
- TNFR:Fc
- TNX-355
- Todoxin
- TSAO derivatives
- Tucaresol
- Vesnarinone
- Vicriviroc
- VIR201
- Virodene P058
- WF10
AV-1101
AV-1101 is an analogue of phenbutazone, a non-steroidal anti-inflammatory that was tested in the late 1980s as an AIDS treatment in France. It has an immunosuppressive effect. It is being developed by A-VIRAL, a Norwegian biotechnology company.
AV-1101 is thought to have two modes of action:
- a direct effect on HIV replication (target site unknown)
- an effect on CD4 cell proliferation by means of preventing lymphocyte activation
Dr Frank Miedema, an immunologist who has published extensively on the mechanisms of CD4 cell loss in HIV disease, has proposed that AV-1101 may be a useful treatment for its ability to remove CD4+RO (memory) cells from the circulation. Miedema has hypothesised that the preponderance of memory cells over naï¶¥ cells suppresses the production of naive cells; if this block is removed by a period of immunosuppressive treatment which can specifically target lymphocytes, naï¶¥ cell production from the bone marrow can be resumed.
In vitro studies suggest a tendency towards neutropenia at doses above 10mg/kg.
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