- 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
MVA-BN-Nef vaccine
MVA-BN-Nef is an experimental therapeutic vaccine. Therapeutic vaccines are being developed for use in HIV-infected people to stimulate the immune system and slow the progression of HIV disease.
MVA-BN-Nef gets its name from the use of a virus vector called modified vaccinia virus Ankara-Bavarian Nordic. This virus vector has been modified so that it expresses the HIV gene nef.
MVA-BN-Nef vaccine has been developed by German researchers led by a team from the University of Erlangen.
Current research
An initial safety study of MVA-BN-Nef vaccine has been conducted in 14 HIV-infected people who were taking highly active antiretroviral therapy (HAART). Immunisation occurred at weeks 0, 4 and 16, and HAART was ceased in all patients two weeks after the third vaccination.
At 18 weeks, a majority of patients experienced improvements in their HIV-specific immune responses. Five people have resumed HAART, but nine remained off treatment after 12 to 28 weeks with an average viral load of 8500 copies/ml. Five of the nine patients had viral loads below pre-HAART levels (Harrer 2003).
Reference
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