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Cited by 299

The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.

Systemic HIV and SIV latency reversal via non-canonical NF-κB signalling in vivo

Open access
Nixon, Christopher C., Mavigner, Maud, Sampey, Gavin C., Brooks, Alyssa D., Spagnuolo, Rae Ann, Irlbeck, David M., Mattingly, Cameron, Ho, Phong T., Schoof, Nils, Cammon, Corinne G., Tharp, Greg K., Kanke, Matthew, Wang, Zhang, Cleary, Rachel A., Upadhyay, Amit A., De, Chandrav, Wills, Saintedym R., Falcinelli, Shane D., Galardi, Cristin, Walum, Hasse, Schramm, Nathaniel J., Deutsch, Jennifer, Lifson, Jeffrey D., Fennessey, Christine M., Keele, Brandon F., Jean, Sherrie, Maguire, Sean, Liao, Baolin, Browne, Edward P., Ferris, Robert G., Brehm, Jessica H., Favre, David, Vanderford, Thomas H., Bosinger, Steven E., Jones, Corbin D., Routy, Jean-Pierre, Archin, Nancie M., Margolis, David M., Wahl, Angela, Dunham, Richard M., Silvestri, Guido, Chahroudi, Ann, Garcia, J. Victor·2020·Nature

Abstract

Long-lasting, latently infected resting CD4+ T cells are the greatest obstacle to obtaining a cure for HIV infection, as these cells can persist despite decades of treatment with antiretroviral therapy (ART). Estimates indicate that more than 70 years of continuous, fully suppressive ART are needed to eliminate the HIV reservoir1. Alternatively, induction of HIV from its latent state could accelerate the decrease in the reservoir, thus reducing the time to eradication. Previous attempts to reactivate latent HIV in preclinical animal models and in clinical trials have measured HIV induction in the peripheral blood with minimal focus on tissue reservoirs and have had limited effect2–9. Here we show that activation of the non-canonical NF-κB signalling pathway by AZD5582 results in the induction of HIV and SIV RNA expression in the blood and tissues of ART-suppressed bone-marrow–liver–thymus (BLT) humanized mice and rhesus macaques infected with HIV and SIV, respectively. Analysis of resting CD4+ T cells from tissues after AZD5582 treatment revealed increased SIV RNA expression in the lymph nodes of macaques and robust induction of HIV in almost all tissues analysed in humanized mice, including the lymph nodes, thymus, bone marrow, liver and lung. This promising approach to latency reversal—in combination with appropriate tools for systemic clearance of persistent HIV infection—greatly increases opportunities for HIV eradication. Activation of the non-canonical NF-κB signalling pathway by AZD5582 results in the induction of HIV and SIV RNA expression in the blood and tissues of antiretroviral-therapy-treated humanized mice and rhesus macaques.

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Authors
Nixon, C. C., Mavigner, M., Sampey, G. C., Brooks, A. D., Spagnuolo, R. A., Irlbeck, D. M., Mattingly, C., Ho, P. T., Schoof, N., Cammon, C. G., Tharp, G. K., Kanke, M., Wang, Z., Cleary, R. A., Upadhyay, A. A., De, C., Wills, S. R., Falcinelli, S. D., Galardi, C., Walum, H., Schramm, N. J., Deutsch, J., Lifson, J. D., Fennessey, C. M., Keele, B. F., Jean, S., Maguire, S., Liao, B., Browne, E. P., Ferris, R. G., Brehm, J. H., Favre, D., Vanderford, T. H., Bosinger, S. E., Jones, C. D., Routy, J.-P., Archin, N. M., Margolis, D. M., Wahl, A., Dunham, R. M., Silvestri, G., Chahroudi, A., & Garcia, J. V.
Venue
Nature
Published
2020-01-22
Volume
578
Issue
7793
Pages
160-165
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W3000922508
Cited by
299
References
51
FWCI
22.03
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Systemic HIV and SIV latency reversal via non-canonical NF-κB signalling in vivo. https://app.cochat.ai/papers/10.1038/s41586-020-1951-3
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Nixon, C. C., Mavigner, M., Sampey, G. C., Brooks, A. D., Spagnuolo, R. A., Irlbeck, D. M., Mattingly, C., Ho, P. T., Schoof, N., Cammon, C. G., Tharp, G. K., Kanke, M., Wang, Z., Cleary, R. A., Upadhyay, A. A., De, C., Wills, S. R., Falcinelli, S. D., Galardi, C., . . . Garcia, J. V. (2020). Systemic HIV and SIV latency reversal via non-canonical NF-κB signalling in vivo. Nature. https://doi.org/10.1038/s41586-020-1951-3

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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