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...

Full description

Bibliographic Details
Main Authors: Melissa B. Uccellini, Sadaf Aslam, Sean T. H. Liu, Fahmida Alam, Adolfo García-Sastre
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Vaccines
Subjects:
Online Access:https://www.mdpi.com/2076-393X/9/6/660
id doaj-e43f319db2504c33994d953592c6bd25
record_format Article
spelling 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 AT melissabuccellini developmentofamacrophagebasedadccassay
AT sadafaslam developmentofamacrophagebasedadccassay
AT seanthliu developmentofamacrophagebasedadccassay
AT fahmidaalam developmentofamacrophagebasedadccassay
AT adolfogarciasastre developmentofamacrophagebasedadccassay
_version_ 1721348796373270528