Immune Recovery Following Autologous Hematopoietic Stem Cell Transplantation in HIV-Related Lymphoma Patients on the BMT CTN 0803/AMC 071 Trial

We report a first in-depth comparison of immune reconstitution in patients with HIV-related lymphoma following autologous hematopoietic cell transplant (AHCT) recipients (n=37, lymphoma, BEAM conditioning), HIV(-) AHCT recipients (n=30, myeloma, melphalan conditioning) at 56, 180, and 365 days post-...

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Veröffentlicht in:Frontiers in immunology 2021-09, Vol.12, p.700045
Hauptverfasser: Shindiapina, Polina, Pietrzak, Maciej, Seweryn, Michal, McLaughlin, Eric, Zhang, Xiaoli, Makowski, Mat, Ahmed, Elshafa Hassan, Schlotter, Sarah, Pearson, Rebecca, Kitzler, Rhonda, Mozhenkova, Anna, Le-Rademacher, Jennifer, Little, Richard F, Akpek, Gorgun, Ayala, Ernesto, Devine, Steven M, Kaplan, Lawrence D, Noy, Ariela, Popat, Uday R, Hsu, Jack W, Morris, Lawrence E, Mendizabal, Adam M, Krishnan, Amrita, Wachsman, William, Williams, Nita, Sharma, Nidhi, Hofmeister, Craig C, Forman, Stephen J, Navarro, Willis H, Alvarnas, Joseph C, Ambinder, Richard F, Lozanski, Gerard, Baiocchi, Robert A
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Sprache:eng
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Zusammenfassung:We report a first in-depth comparison of immune reconstitution in patients with HIV-related lymphoma following autologous hematopoietic cell transplant (AHCT) recipients (n=37, lymphoma, BEAM conditioning), HIV(-) AHCT recipients (n=30, myeloma, melphalan conditioning) at 56, 180, and 365 days post-AHCT, and 71 healthy control subjects. Principal component analysis showed that immune cell composition in HIV(+) and HIV(-) AHCT recipients clustered away from healthy controls and from each other at each time point, but approached healthy controls over time. Unsupervised feature importance score analysis identified activated T cells, cytotoxic memory and effector T cells [higher in HIV(+)], and naïve and memory T helper cells [lower HIV(+)] as a having a significant impact on differences between HIV(+) AHCT recipient and healthy control lymphocyte composition (p
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.700045