Identification of Genetically Intact HIV-1 Proviruses in Specific CD4+ T Cells from Effectively Treated Participants

Bonnie Hiener(The University of Sydney), Bethany A. Horsburgh(The University of Sydney), John‐Sebastian Eden(The University of Sydney), Kirston Barton(The University of Sydney), Timothy E. Schlub(The University of Sydney), Eunok Lee(The University of Sydney), Susanne von Stockenström(Karolinska University Hospital), Lina Odevall(Karolinska University Hospital), Jeffrey M. Milush(University of California, San Francisco), Teri Liegler(University of California, San Francisco), Elizabeth Sinclair(University of California, San Francisco), Rebecca Hoh(University of California, San Francisco), Eli Boritz(National Institute of Allergy and Infectious Diseases), Daniel C. Douek(National Institute of Allergy and Infectious Diseases), Rémi Fromentin(Centre Hospitalier de l’Université de Montréal), Nicolas Chomont(Centre Hospitalier de l’Université de Montréal), Steven G. Deeks(University of California, San Francisco), Frederick Hecht(University of California, San Francisco), Sarah Palmer(The University of Sydney)
Cell Reports
October 1, 2017
Cited by 388Open Access
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Abstract

T cell subsets in six individuals on long-term ART. FLIPS is an efficient, high-throughput assay that amplifies and sequences near full-length (∼9 kb) HIV-1 proviral genomes and determines potential replication competency through genetic characterization. FLIPS provides a genome-scale perspective that addresses the limitations of other methods that also genetically characterize the latent reservoir. Using FLIPS, we identified 5% of proviruses as intact and potentially replication competent. Intact proviruses were unequally distributed between T cell subsets, with effector memory cells containing the largest proportion of genetically intact HIV-1 proviruses. We identified multiple identical intact proviruses, suggesting a role for cellular proliferation in the maintenance of the latent HIV-1 reservoir.


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