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Bispecific antibody-activated T cells enhance NK cell-mediated antibody-dependent cellular cytotoxicity
Journal article   Open access   Peer reviewed

Bispecific antibody-activated T cells enhance NK cell-mediated antibody-dependent cellular cytotoxicity

Zhaoming Wang, Chaobo Yin, Lawrence G Lum, Andrean Simons and George J Weiner
Journal of hematology and oncology, Vol.14(1), pp.204-204
12/09/2021
DOI: 10.1186/s13045-021-01216-w
PMCID: PMC8656063
PMID: 34886888
url
https://doi.org/10.1186/s13045-021-01216-wView
Published (Version of record) Open Access

Abstract

Resistance to anti-cancer monoclonal antibody (mAb) therapy remains a clinical challenge. Previous work in our laboratory has shown that T cell help in the form of interleukin-2 maintains long-term NK cell viability and NK cell-mediated antibody-dependent cellular cytotoxicity (ADCC). Lack of such T cell help may be a potential mechanism for resistance to mAb therapy. Here, we evaluate whether concomitant treatment with anti-CD3 × anti-cancer bispecific antibodies (bsAbs) can overcome this resistance by enhancing T cell help, and thereby maintaining long-term NK cell-mediated ADCC. Normal donor peripheral blood mononuclear cells were depleted of T cells, replenished with defined numbers of autologous T cells (from 0.75 to 50%) and co-cultured with mono-/bispecific antibody-treated target tumor cells for up to 7 days. At low T cell concentrations, bsAb-activated T cells (mainly CD4 T cells) were more effective than resting T cells at maintaining NK cell viability and ADCC. Brief (4 h to 2 day) bsAb exposure was sufficient to enhance long-term ADCC by NK cells. These findings raise the hypothesis that local T cell activation mediated by systemic treatment with anti-CD3 X anti-cancer bsAb may enhance the anti-tumor efficacy of monospecific mAbs that mediate their primary therapeutic effect via NK-mediated ADCC.
Antibodies, Bispecific - pharmacology Antibody-Dependent Cell Cytotoxicity - drug effects Antineoplastic Agents, Immunological - pharmacology Cells, Cultured Humans Killer Cells, Natural - drug effects Killer Cells, Natural - immunology Lymphocyte Activation - drug effects T-Lymphocytes - immunology

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