TY - JOUR
T1 - Murine models for evaluating antiretroviral therapy
AU - Ruprecht, Ruth M.
AU - Bernard, Lisa D.
AU - Chou, Ting Chao
AU - Gama Sosa, Miguel A.
AU - Fazely, Fatemeh
AU - Koch, John
AU - Sharma, Prem L.
AU - Mullaney, Steve
PY - 1990/9/1
Y1 - 1990/9/1
N2 - The pandemic of the acquired immunodeficiency syndrome (AIDS), caused by the human immunodeficiency virus type 1 (HIV-1), requires rapid development of effective therapy and prevention. Analysis of candidate anti-HIV-1 drugs in animals is problematic since no ideal animal model for HIV-1 infection and disease exists. For many reasons, including small size, availability of inbred strains, immunological reagents, and lymphokines, murine systems have been used for in vivo analysis of antiretroviral agents. Here we review currently available murine models involving HIV-1 in transgenic mice and in chimeric mice reconstituted with human cells, as well as murine systems using retroviruses of the subfamily Oncovirinae rather than Lentivirinae. We report our results on various antiretroviral treatment strategies, including chemoprophylaxis after acute retroviral exposure, therapy of chronic viremia, quantitative analysis of combination therapy, and therapy during pregnancy and in the neonatal period aimed at preventing viremia in the offspring. Due to our highly effective postexposure treatment protocols with 3′-azido-3′-deoxythymidine (zidovudine)combined with recombinant human interferon-αA/D, retrovirus-inoculated mice developed immunity to the virus to which they were exposed, which will allow us to determine the nature of protective antiretroviral immunity in inbred mice.
AB - The pandemic of the acquired immunodeficiency syndrome (AIDS), caused by the human immunodeficiency virus type 1 (HIV-1), requires rapid development of effective therapy and prevention. Analysis of candidate anti-HIV-1 drugs in animals is problematic since no ideal animal model for HIV-1 infection and disease exists. For many reasons, including small size, availability of inbred strains, immunological reagents, and lymphokines, murine systems have been used for in vivo analysis of antiretroviral agents. Here we review currently available murine models involving HIV-1 in transgenic mice and in chimeric mice reconstituted with human cells, as well as murine systems using retroviruses of the subfamily Oncovirinae rather than Lentivirinae. We report our results on various antiretroviral treatment strategies, including chemoprophylaxis after acute retroviral exposure, therapy of chronic viremia, quantitative analysis of combination therapy, and therapy during pregnancy and in the neonatal period aimed at preventing viremia in the offspring. Due to our highly effective postexposure treatment protocols with 3′-azido-3′-deoxythymidine (zidovudine)combined with recombinant human interferon-αA/D, retrovirus-inoculated mice developed immunity to the virus to which they were exposed, which will allow us to determine the nature of protective antiretroviral immunity in inbred mice.
UR - http://www.scopus.com/inward/record.url?scp=0025121540&partnerID=8YFLogxK
M3 - Article
C2 - 2167158
AN - SCOPUS:0025121540
SN - 0008-5472
VL - 50
SP - 5618s-5627s
JO - Cancer Research
JF - Cancer Research
IS - 17 SUPPL.
ER -