Comparison of antibody response elicited after mRNA-1273 heterologous boost in HIV-negative participants and PLWH.

<p>The binding (Panel A and D), neutralization (Panel B and C) and ADCC (Panel C and F) were measured in individuals who were HIV-negative and people living with HIV (PLWH). Comparisons were separated based on number of Ad26.COV2.S with 1 doses Ad26.COV2.S (Panels A-C) and 2 doses of Ad26.COV2.S (Panels D-F). The plasma neutralization titer is measured as an ID<sub>50</sub>. Black horizontal bars represent medians. The threshold of detection for the neutralization assay is an ID<sub>50</sub> of 20. Antibody binding was measured using an in-house SARS-CoV-2 assay using the D614G full spike protein. An EC50 was used to measure the binding titers of the samples. ADCC activity was measured by detecting the crosslinking ability of the antibodies present in the serum. Relative light units were measured which correlate with the levels of FcγRIIIa signalling. For all assays, statistical significance was measured with the Kruskal-Wallis test with Dunn’s multiple comparisons test. Significance is shown as: *p < 0.05, **p < 0.01, ***p < 0.001 and ****p < 0.0001. Medians and fold changes are depicted under each graph. Samples were run in duplicate for all assays.</p> <p>(DOCX)</p>

Publication Details

Journal
Figshare
Published
2024-12-05
DOI
https://doi.org/10.1371/journal.pgph.0003260.s015
Primary Topic
Monoclonal and Polyclonal Antibodies Research
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article
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article

Comparison of antibody response elicited after mRNA-1273 heterologous boost in HIV-negative participants and PLWH.

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Monoclonal and Polyclonal Antibodies Research
article

Comparison of antibody response elicited after mRNA-1273 heterologous boost in HIV-negative participants and PLWH.

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Abstract

<p>The binding (Panel A and D), neutralization (Panel B and C) and ADCC (Panel C and F) were measured in individuals who were HIV-negative and people living with HIV (PLWH). Comparisons were separated based on number of Ad26.COV2.S with 1 doses Ad26.COV2.S (Panels A-C) and 2 doses of Ad26.COV2.S (Panels D-F). The plasma neutralization titer is measured as an ID<sub>50</sub>. Black horizontal bars represent medians. The threshold of detection for the neutralization assay is an ID<sub>50</sub> of 20. Antibody binding was measured using an in-house SARS-CoV-2 assay using the D614G full spike protein. An EC50 was used to measure the binding titers of the samples. ADCC activity was measured by detecting the crosslinking ability of the antibodies present in the serum. Relative light units were measured which correlate with the levels of FcγRIIIa signalling. For all assays, statistical significance was measured with the Kruskal-Wallis test with Dunn’s multiple comparisons test. Significance is shown as: *p < 0.05, **p < 0.01, ***p < 0.001 and ****p < 0.0001. Medians and fold changes are depicted under each graph. Samples were run in duplicate for all assays.</p> <p>(DOCX)</p>

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