Development of a Macrophage-Based ADCC Assay
Fc-dependent effector functions are an important determinant of the in vivo potency of therapeutic antibodies. Effector function is determined by the combination of FcRs bound by the antibody and the cell expressing the relevant FcRs, leading to antibody-dependent cellular cytotoxicity (ADCC). A num...
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doaj-e43f319db2504c33994d953592c6bd252021-07-01T00:24:06ZengMDPI AGVaccines2076-393X2021-06-01966066010.3390/vaccines9060660Development of a Macrophage-Based ADCC AssayMelissa B. Uccellini0Sadaf Aslam1Sean T. H. Liu2Fahmida Alam3Adolfo García-Sastre4Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USADepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USADepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USADepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USADepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USAFc-dependent effector functions are an important determinant of the in vivo potency of therapeutic antibodies. Effector function is determined by the combination of FcRs bound by the antibody and the cell expressing the relevant FcRs, leading to antibody-dependent cellular cytotoxicity (ADCC). A number of ADCC assays have been developed; however, they suffer from limitations in terms of throughput, reproducibility, and in vivo relevance. Existing assays measure NK cell-mediated ADCC activity; however, studies suggest that macrophages mediate the effector function of many antibodies in vivo. Here, we report the development of a macrophage-based ADCC assay that relies on luciferase expression in target cells as a measure of live cell number. In the presence of primary mouse macrophages and specific antibodies, loss of luciferase signal serves as a surrogate for ADCC-dependent killing. We show that the assay functions for a variety of mouse and human isotypes with a model antigen/antibody complex in agreement with the known effector function of the isotypes. We also use this assay to measure the activity of a number of influenza-specific antibodies and show that the assay correlates well with the known in vivo effector functions of these antibodies.https://www.mdpi.com/2076-393X/9/6/660ADCCmacrophageinfluenzahemagglutinin |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Melissa B. Uccellini Sadaf Aslam Sean T. H. Liu Fahmida Alam Adolfo García-Sastre |
spellingShingle |
Melissa B. Uccellini Sadaf Aslam Sean T. H. Liu Fahmida Alam Adolfo García-Sastre Development of a Macrophage-Based ADCC Assay Vaccines ADCC macrophage influenza hemagglutinin |
author_facet |
Melissa B. Uccellini Sadaf Aslam Sean T. H. Liu Fahmida Alam Adolfo García-Sastre |
author_sort |
Melissa B. Uccellini |
title |
Development of a Macrophage-Based ADCC Assay |
title_short |
Development of a Macrophage-Based ADCC Assay |
title_full |
Development of a Macrophage-Based ADCC Assay |
title_fullStr |
Development of a Macrophage-Based ADCC Assay |
title_full_unstemmed |
Development of a Macrophage-Based ADCC Assay |
title_sort |
development of a macrophage-based adcc assay |
publisher |
MDPI AG |
series |
Vaccines |
issn |
2076-393X |
publishDate |
2021-06-01 |
description |
Fc-dependent effector functions are an important determinant of the in vivo potency of therapeutic antibodies. Effector function is determined by the combination of FcRs bound by the antibody and the cell expressing the relevant FcRs, leading to antibody-dependent cellular cytotoxicity (ADCC). A number of ADCC assays have been developed; however, they suffer from limitations in terms of throughput, reproducibility, and in vivo relevance. Existing assays measure NK cell-mediated ADCC activity; however, studies suggest that macrophages mediate the effector function of many antibodies in vivo. Here, we report the development of a macrophage-based ADCC assay that relies on luciferase expression in target cells as a measure of live cell number. In the presence of primary mouse macrophages and specific antibodies, loss of luciferase signal serves as a surrogate for ADCC-dependent killing. We show that the assay functions for a variety of mouse and human isotypes with a model antigen/antibody complex in agreement with the known effector function of the isotypes. We also use this assay to measure the activity of a number of influenza-specific antibodies and show that the assay correlates well with the known in vivo effector functions of these antibodies. |
topic |
ADCC macrophage influenza hemagglutinin |
url |
https://www.mdpi.com/2076-393X/9/6/660 |
work_keys_str_mv |
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