Productive and latent HIV infections originate in resting CD4<sup>+</sup>T cells
Summary Productively and latently HIV-infected cells are the source of virus that respectively establishes and sustains systemic infections and the reservoir in which HIV persists and rebounds when anti-retroviral therapy (ART) is interrupted. While infected activated CD4+T cells are thought to be the principal source of HIV production, and reversion of activated infected cells to a resting state as the major pathway to establishment of the latently infected cell reservoir, we now show that in the earliest stages of detectable HIV infection in the lymphoid tissue reservoir, infection of resting CD4+T cells establishes the first populations of both productively and latently infected cells. We further show that the early infection of resting T cells reflects their predominance in lymphoid tissues and the expression of pTEFb in vivo in resting T cells to support their infection. The immediate establishment of productively and latently infected cell populations enable HIV to propagate and persist, and generates reservoirs from which infection can rebound despite instituting ART at the earliest stage of detectable infection..
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Preprint| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
bioRxiv.org - (2023) vom: 16. Feb. Zur Gesamtaufnahme - year:2023 |
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| Sprache: |
Englisch |
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| Beteiligte Personen: |
Wietgrefe, Stephen W. [VerfasserIn] |
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| Links: |
Volltext [kostenfrei] |
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| doi: |
10.1101/2022.08.26.505461 |
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| PPN (Katalog-ID): |
XBI037063316 |
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| 245 | 1 | 0 | |a Productive and latent HIV infections originate in resting CD4<sup>+</sup>T cells |
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| 520 | |a Summary Productively and latently HIV-infected cells are the source of virus that respectively establishes and sustains systemic infections and the reservoir in which HIV persists and rebounds when anti-retroviral therapy (ART) is interrupted. While infected activated CD4+T cells are thought to be the principal source of HIV production, and reversion of activated infected cells to a resting state as the major pathway to establishment of the latently infected cell reservoir, we now show that in the earliest stages of detectable HIV infection in the lymphoid tissue reservoir, infection of resting CD4+T cells establishes the first populations of both productively and latently infected cells. We further show that the early infection of resting T cells reflects their predominance in lymphoid tissues and the expression of pTEFb in vivo in resting T cells to support their infection. The immediate establishment of productively and latently infected cell populations enable HIV to propagate and persist, and generates reservoirs from which infection can rebound despite instituting ART at the earliest stage of detectable infection. | ||
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| 700 | 1 | |a Duan, Lijie |4 aut | |
| 700 | 1 | |a Southern, Peter J. |4 aut | |
| 700 | 1 | |a Zuck, Paul |4 aut | |
| 700 | 1 | |a Wu, Guoxin |4 aut | |
| 700 | 1 | |a Howell, Bonnie J. |4 aut | |
| 700 | 1 | |a Reilly, Cavan |4 aut | |
| 700 | 1 | |a Kroon, Eugène |4 aut | |
| 700 | 1 | |a Chottanapund, Suthat |4 aut | |
| 700 | 1 | |a Buranapraditkun, Supranee |4 aut | |
| 700 | 1 | |a Sacdalan, Carlo |4 aut | |
| 700 | 1 | |a Tulmethakaan, Nicha |4 aut | |
| 700 | 1 | |a Colby, Donn J. |4 aut | |
| 700 | 1 | |a Chomchey, Nitiya |4 aut | |
| 700 | 1 | |a Prueksakaew, Peeriya |4 aut | |
| 700 | 1 | |a Pinyakorn, Suteeraporn |4 aut | |
| 700 | 1 | |a Trichavaroj, Rapee |4 aut | |
| 700 | 1 | |a Hsu, Denise |4 aut | |
| 700 | 1 | |a Vasan, Sandhya |4 aut | |
| 700 | 1 | |a Manasnayakorn, Sopark |4 aut | |
| 700 | 1 | |a de Souza, Mark |4 aut | |
| 700 | 1 | |a Tovanabutra, Sodsai |4 aut | |
| 700 | 1 | |a Schuetz, Alexandra |4 aut | |
| 700 | 1 | |a Robb, Merlin L. |4 aut | |
| 700 | 1 | |a Phanuphak, Nittaya |4 aut | |
| 700 | 1 | |a Ananworanich, Jintanat |4 aut | |
| 700 | 1 | |a Schacker, Timothy W. |4 aut | |
| 700 | 1 | |a Haase, Ashley T. |0 (orcid)0000-0002-5374-2388 |4 aut | |
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