A significant hurdle in the field of HIV vaccine design is the enormous diversity of the circulating virus. Mutations occur within an infected subject and are then transmitted to the next host making the task of generating a single vaccine that prevents infection from an ever-evolving virus more challenging. In this application, we seek to have a better understanding of the mutations occurring in the virus that are then transmitted to another individual and whether or not these mutations should be targeted by a vaccine. We hypothesize that some mutations that occur and persist in the viral sequence of HIV may be able to elicit an effective immune response and that designing vaccines to recognize virus encoding these mutations will be beneficial. To prove this hypothesis, we seek to evaluate the frequency and quality of CD8 T cell responses to mutated and non-mutated sequences in chronically HIV infected subjects. These data will be compared with the level of viral control at apopulation level to determine the contribution of immune responses targeting mutated virus to viral replication. A score for each epitope will be calculated based a number of characteristics with high scoring epitopes being ideal for vaccine inclusion. In the second aim, we will sequence the virus in primary HIV infection to determine the frequency of mutated and non-mutated sequences encoded by the single infecting viral strain. We will then examine the frequency and quality of CD8 T cells targeting the mutated or nonmutated sequences. We expect to find that targeting some mutated sequences will be beneficial while other sequences will elicit poor quality or no response at all. These results will inform the design of future vaccines by defining specific viral sequences to target or exclude. Finally, in the last aim, we will evaluate the capacity of a mosaic vaccine to elicit immune responses that recognize mutated virus. Mosaic vaccines are designed to have viral sequences that encode non-mutated and common mutants to increase the number of immune responses elicited in the vaccinee. We will enumerate the frequency and determine the quality of the responses generated as a result of this vaccine construct. Taken together, this proposal will determine the biologic significance of immune responses recognizing mutated virus in context of HIV infection and vaccination. Such information will be extremely pertinent for future HIV-1 vaccine design and efficacy testing.
Despite over two decades of research in the field of HIV treatment and vaccine development, strategies for a cure and preventive vaccine remain elusive. A vaccine remains the best hope to curb this epidemic. This application serves to understand mutations in HIV, the ability of the immune systems to recognize these mutations, and the importance of designing HIV-1 vaccines to target these sites of frequent HIV mutations.
| Peng, Binghao J; Carlson, Jonathan M; Liu, Michael K P et al. (2018) Antisense-Derived HIV-1 Cryptic Epitopes Are Not Major Drivers of Viral Evolution during the Acute Phase of Infection. J Virol 92: |
| Carlson, Jonathan M; Du, Victor Y; Pfeifer, Nico et al. (2016) Impact of pre-adapted HIV transmission. Nat Med 22:606-13 |
| Bansal, Anju; Sterrett, Sarah; Erdmann, Nathan et al. (2015) Normal T-cell activation in elite controllers with preserved CD4+ T-cell counts. AIDS 29:2245-54 |
