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. 2023 Feb 23;14:1041. doi: 10.1038/s41467-023-36683-x

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© The Author(s) 2023

Open Access 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/.

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Fig. 4 — a–d An anti-AD-6 polyclonal antibody was assayed by ELISA for binding to AD-6 polypeptide (a), vaccine gB (b), a commercial recombinant gB produced in E. coli (c) or CMV virions (d). Antibody levels are represented in function of absorbance (450 nm) per concentration of primary antibody in μg/mL and is representative of three independent experiments. Each data point represents mean + SEM of antibodies purified from two immunized rabbits. e Flow cytometry analysis of mock-infected and CMV-infected cells with anti-AD-6 pAb or non-specific rabbit IgG 3 days post infection. Gated on single, live cells and HLA class I expression to identify virally infected cells.