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. 2021 Jun 28;18:17. doi: 10.1186/s12977-021-00560-6

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Neutralisation of HIV-1 pseudoviruses by pN6. A Neutralisation by pN6 was assessed against a panel of 10 HIV-1 ENV pseudoviruses, and HIV-1 strain BaL.26 as an internal control, using TZM-bl cells. pN6 neutralisation assay was carried out in triplicate, and mN6 BaL.26 set was carried out in duplicate. B Correlation of published mN6 IC₅₀s with pN6 IC₅₀s from pseudovirus neutralisation assay. Open circle denotes assay-derived IC₅₀ of pN6 compared with mN6 for BaL.26, rather than published value, as an internal control. Pearson correlation analysis calculated r value of 0.92 (p ≤ 0.0001)