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Ablation of CD8+ T cell recognition of an immunodominant epitope in SARS-CoV-2 Omicron variants BA.1, BA.2 and BA.3

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posted on 2023-06-16, 00:19 authored by Srividhya Swaminathan, Katie E Lineburg, Archana Panikkar, Jyothy Raju, Lawton MurdoloLawton Murdolo, Christopher SzetoChristopher Szeto, Pauline Crooks, Laetitia Le Texier, Sweera Rehan, Michael Dewar-OldisMichael Dewar-Oldis, Peter BarnardPeter Barnard, George R Ambalathingal, Michelle A Neller, Kirsty R Short, Stephanie GrasStephanie Gras, Rajiv Khanna, Corey Smith
The emergence of the SARS-CoV-2 Omicron variant has raised concerns of escape from vaccine-induced immunity. A number of studies have demonstrated a reduction in antibody-mediated neutralization of the Omicron variant in vaccinated individuals. Preliminary observations have suggested that T cells are less likely to be affected by changes in Omicron. However, the complexity of human leukocyte antigen genetics and its impact upon immunodominant T cell epitope selection suggests that the maintenance of T cell immunity may not be universal. In this study, we describe the impact that changes in Omicron BA.1, BA.2 and BA.3 have on recognition by spike-specific T cells. These T cells constitute the immunodominant CD8+ T cell response in HLA-A*29:02+ COVID-19 convalescent and vaccinated individuals; however, they fail to recognize the Omicron-encoded sequence. These observations demonstrate that in addition to evasion of antibody-mediated immunity, changes in Omicron variants can also lead to evasion of recognition by immunodominant T cell responses.

Funding

This work was supported by generous donations to the QIMR Berghofer COVID-19 appeal and the Medical Research Future Fund (MRFF, APP2005654). SS is supported by Australian Government Research Training Program Scholarship and QIMR Berghofer Top-Up Scholarship award. SG is an NHMRC SRF-A Fellow (1159272). KRS is supported by an NHMRC Investigator Grant (2007919).

History

Publication Date

2022-10-27

Journal

Nature Communications

Volume

13

Article Number

6387

Pagination

6p. (p. 1-6)

Publisher

Springer Nature

ISSN

2041-1723

Rights Statement

This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing,adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2022

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