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Dynamic MAIT cell response with progressively enhanced innateness during acute HIV-1 infection

Lal, KG (author)
Karolinska Institutet
Kim, D (author)
Costanzo, MC (author)
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Creegan, M (author)
Leeansyah, E (author)
Dias, J (author)
Paquin-Proulx, D (author)
Eller, LA (author)
Schuetz, A (author)
Phuang-ngern, Y (author)
Krebs, SJ (author)
Slike, BM (author)
Kibuuka, H (author)
Maganga, L (author)
Nitayaphan, S (author)
Kosgei, J (author)
Sacdalan, C (author)
Ananworanich, J (author)
Bolton, DL (author)
Michael, NL (author)
Shacklett, BL (author)
Robb, ML (author)
Eller, MA (author)
Sandberg, JK (author)
Karolinska Institutet
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 (creator_code:org_t)
2020-01-14
2020
English.
In: Nature communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 11:1, s. 272-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Mucosa-associated invariant T (MAIT) cell loss in chronic HIV-1 infection is a significant insult to antimicrobial immune defenses. Here we investigate the response of MAIT cells during acute HIV-1 infection utilizing the RV217 cohort with paired longitudinal pre- and post-infection samples. MAIT cells are activated and expand in blood and mucosa coincident with peak HIV-1 viremia, in a manner associated with emerging microbial translocation. This is followed by a phase with elevated function as viral replication is controlled to a set-point level, and later by their functional decline at the onset of chronic infection. Interestingly, enhanced innate-like pathways and characteristics develop progressively in MAIT cells during infection, in parallel with TCR repertoire alterations. These findings delineate the dynamic MAIT cell response to acute HIV-1 infection, and show how the MAIT compartment initially responds and expands with enhanced function, followed by progressive reprogramming away from TCR-dependent antibacterial responses towards innate-like functionality.

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