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Preferential and persistent impact of acute HIV-1 infection on CD4+ iNKT cells in colonic mucosa

Paquin-Proulx, D (author)
Lal, KG (author)
Phuang-Ngern, Y (author)
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Creegan, M (author)
Tokarev, A (author)
Suhkumvittaya, S (author)
Alrubayyi, A (author)
Kroon, E (author)
Pinyakorn, S (author)
Slike, BM (author)
Bolton, DL (author)
Krebs, SJ (author)
Eller, LA (author)
Sajjaweerawan, C (author)
Pagliuzza, A (author)
Chomont, N (author)
Rerknimitr, R (author)
Chomchey, N (author)
Phanuphak, N (author)
de Souza, MS (author)
Michael, NL (author)
Robb, ML (author)
Ananworanich, J (author)
Sandberg, JK (author)
Karolinska Institutet
Eller, MA (author)
Schuetz, A (author)
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 (creator_code:org_t)
2021-11-09
2021
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 1091-6490. ; 118:46
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Evidence suggests that HIV-1 disease progression is determined in the early stages of infection. Here, preinfection invariant natural killer T (iNKT) cell levels were predictive of the peak viral load during acute HIV-1 infection (AHI). Furthermore, iNKT cells were preferentially lost in AHI. This was particularly striking in the colonic mucosa, where iNKT cells were depleted more profoundly than conventional CD4+T cells. The initiation of antiretroviral therapy during AHI-prevented iNKT cell dysregulation in peripheral blood but not in the colonic mucosa. Overall, our results support a model in which iNKT cells are early and preferential targets for HIV-1 infection during AHI.

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