| Literature DB >> 24948736 |
Theodora Hatziioannou1, Gregory Q Del Prete2, Brandon F Keele2, Jacob D Estes2, Matthew W McNatt3, Julia Bitzegeio3, Alice Raymond4, Anthony Rodriguez4, Fabian Schmidt3, C Mac Trubey2, Jeremy Smedley5, Michael Piatak2, Vineet N KewalRamani6, Jeffrey D Lifson7, Paul D Bieniasz8.
Abstract
Primate lentiviruses exhibit narrow host tropism, reducing the occurrence of zoonoses but also impairing the development of optimal animal models of AIDS. To delineate the factors limiting cross-species HIV-1 transmission, we passaged a modified HIV-1 in pigtailed macaques that were transiently depleted of CD8(+) cells during acute infection. During adaptation over four passages in macaques, HIV-1 acquired the ability to antagonize the macaque restriction factor tetherin, replicated at progressively higher levels, and ultimately caused marked CD4(+) T cell depletion and AIDS-defining conditions. Transient treatment with an antibody to CD8 during acute HIV-1 infection caused rapid progression to AIDS, whereas untreated animals exhibited an elite controller phenotype. Thus, an adapted HIV-1 can cause AIDS in macaques, and stark differences in outcome can be determined by immunological perturbations during early infection.Entities:
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Year: 2014 PMID: 24948736 PMCID: PMC4266393 DOI: 10.1126/science.1250761
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728