Ebola virus shed glycoprotein is toxic to human T, B, and natural killer lymphocytes.

Publication Type Academic Article
Authors Perez-Valencia L, Vannella K, Ramos-Benitez M, Sun J, Abu-Asab M, Dorward D, Awad K, Platt A, Jacobson E, Kindrachuk J, Chertow D
Journal iScience
Volume 26
Issue 8
Pagination 107323
Date Published 07/11/2023
ISSN 2589-0042
Abstract Lymphocyte depletion is a distinctive feature of Ebola virus (EBOV) disease. The ectodomain of EBOV glycoprotein (GP) is cleaved off the surface of infected cells into circulation as shed GP. To test the hypothesis that shed GP induces lymphocyte death, we cultured primary human B, NK, or T cells with shed GP in vitro. We found that shed GP dependably decreased B, NK, and T cell viability across donors. B and NK cells exhibited higher susceptibility than T cells. Continuous monitoring revealed shed GP began to kill B and NK cells by 4 h and T cells by 5 h. We also demonstrated that shed GP-induced lymphocyte death can be both caspase dependent and caspase independent. Our data are evidence that the cytotoxic effect of shed GP on lymphocytes may contribute to EBOV disease and highlight the need for further research to clarify mechanisms of shed GP-induced death.
DOI 10.1016/j.isci.2023.107323
PubMed ID 37529105
PubMed Central ID PMC10387567
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