Clonal integration site expansion of infected cells is a main contributor of HIV persistence in more differentiated T cell subsets during suppressive ART von Symons, J., Bacchus-Souffan, C., Chopra, A., Leary, S., Cameron, D., Cameron, P.U., Hoh, R., Ahn, H., Deeks, S.G., McCune, J.M., Mallal, S., Hunt, P.W., Lewin, S.R.

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OA3-3 Anti-PD-1 disrupts HIV latency in non-proliferating but not in proliferating T cells von Van der Sluis, R.M., Kumar, N.A., Evans, V.A., Dantanarayana, A.I., Sékaly, R.P., Fromentin, R., Chomont, N., Cameron, P.U., Lewin, S.R.

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31 High prevalence of CXCR4-using virus and low clonal expansion in infected naïve and central memory CD4+ T cells in individuals on ART von Roche, M., Tumpach, C., Symons, J., Cameron, P.U., Churchill, M.J., Deeks, S.G., Gorry, P.R., Lewin, S.R.

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The CCR5-agonist maraviroc reverses HIV latency, results from ex vivo studies and a randomized placebo controlled clinical trial von Symons, J., van Lelyveld, S.F.L., de Spiegelaere, W., Wensing, A.M.J., Drylewicz, J., Hoepelman, A.I.M., Cameron, P.U., Lu, H., Mota, T., Dantanarayana, A.I., Vandekerckhove, L., Lewin, S.R., Tesselaar, K., Nijhuis, M.

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Co-culture of T-cells with dendritic cells facilitates HIV latency in proliferating CD4 + T-cells: implications for the establishment and reversal of latency von Kumar, N., van der Sluis, R.M., Mota, T., Evans, V.A., Lewin, S.R., Cameron, P.U.

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32 Plasmacytoid DCs control HIV latency in resting T cells by type I IFNα von Van der Sluis, R.M., Mota, T., Kumar, N.A., Evans, V.A., Harman, A.N., Tennakoon, S., Deeks, S.G., Herzog, P., Lewin, S.R., Cameron, P.U.

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8 IFNα activates latent HIV-1 in non-proliferating latently infected T-cells von Sluis, R.M., Kumar, N.A., Evans, V.A., Harman, A.N., Mota, T., Tennakoon, S., Herzog, P., Lewin, S.R., Cameron, P.U.

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23 Understanding the effects of latency reversing agents on HIV RNA splicing: implications for latency reversal von Mota, T.M., Khoury, G., Jacobson, J.C., Lu, H.K., Wightman, F., Sluis, d.e.r., Anderson, J.L., Cameron, P.U., Lewin, S.R., Purcell, D.F.J., Van, R.M.

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564 HIV INFECTION OF CHRONICALLY HEPATITIS B VIRUS (HBV)-INFECTED HUMAN HEPATIC AND STELLATE CELL LINES: IMPLICATIONS FOR PATHOGENESIS OF HIV-HBV CO-INFECTION von Iser, D.M, Solomon, A, Saleh, S, Warner, N, Sievert, W, Cameron, P.U, Desmond, P.V, Locarnini, S.A, Lewin, S.R

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The role of SNPs in the α-chain of the IL-7R gene in CD4+ T-cell recovery in HIV-infected African patients receiving suppressive cART von Rajasuriar, R, Booth, D R, Gouillou, M, Spelman, T, James, I, Solomon, A, Chua, K, Stewart, G, Deeks, S, Bangsberg, D R, Muzoora, C, Cameron, P U, Hunt, P, Martin, J, Lewin, S R

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Conjugates of dendritic cells and memory T lymphocytes from skin facilitate productive infection with HIV-1 von Pope, M., Betjes, M.G.H., Romani, N., Hirmand, H., Cameron, P.U., Hoffman, L., Gezelter, S., Schuler, G., Steinman, R.M.

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Conservation of the central MHC genome: PFGE mapping and RFLP analysis of complement, HSP70, and TNF genes in the goat von CAMERON, P. U, TABARIAS, H. A, PULENDRAN, B, ROBINSON, W, DAWKINS, R. L

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Major histocompatibility complex genes influence the outcome of HIV infection: Ancestral haplotypes with C4 null alleles explain diverse HLA associations von Cameron, P.U., Mallal, S.A., French, M.A.H., Dawkins, R.L.

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Some disease-associated ancestral haplotypes carry a polymorphism of TNF von Dawkins, R.L., Leaver, A., Cameron, P.U., Martin, E., Kay, P.H., Christiansen, F.T.

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MHC genes and HIV infection von Mallal, S, Cameron, P.U, French, M.A.H, Dawkins, R.L

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Major histocompatibility complex genes influence the outcome of HIV infection von Cameron, P.U., Mallal, S.A., French, M.A.H., Dawkins, R.L.

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Major histocompatibility complex ancestral haplotypes in the chimpanzee: Identification using C4 allotyping von Christiansen, F.T., Bontrop, R.E., Giphart, M., Cameron, P.U., Zhang, W.J., Townend, D., Jonker, M., Dawkins, R.L.

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Periodontal attachment loss in HIV-infected patients is associated with the major histocompatibility complex 8.1 haplotype (HLA-A1,B8,DR3) von Price, P., Calder, D.M., Witt, C.S., Allcock, R.J.N., Christiansen, F.T., Davies, G.R., Cameron, P.U., Rogers, M., Baluchova, K., Moore, C.B., French, M.A.

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The uptake of horseradish peroxidase by cortical synapses in rat brain. An in vivo study von Jones, D G, Cameron, P U, Ellison, L T

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Stimulation-induced uptake of horseradish peroxidase by rat cortical synapses von Cooke, C.T., Cameron, P.U., Jones, D.G.

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