Affiliation:
1. Department of Zoology, University of Oxford, Oxford OX1 3PS, UK
2. Nuffield Department of Clinical Medicine, University of Oxford, Oxford OX3 7BN, UK
Abstract
Despite substantial advances in our knowledge of immune responses against HIV-1 and of its evolution within the host, it remains unclear why control of the virus eventually breaks down. Here, we present a new theoretical framework for the infection dynamics of HIV-1 that combines antibody and CD8
+
T-cell responses, notably taking into account their different lifespans. Several apparent paradoxes in HIV pathogenesis and genetics of host susceptibility can be reconciled within this framework by assigning a crucial role to antibody responses in the control of viraemia. We argue that, although escape from or progressive loss of quality of CD8
+
T-cell responses can accelerate disease progression, the underlying cause of the breakdown of virus control is the loss of antibody induction due to depletion of CD4
+
T cells. Furthermore, strong antibody responses can prevent CD8
+
T-cell escape from occurring for an extended period, even in the presence of highly efficacious CD8
+
T-cell responses.
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Cited by
6 articles.
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