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Updated: Apr 27, 2026

Measurement of Natural Killer Cell-Mediated Cytotoxicity and Migration in the Context of Hepatic Tumor Cells
Published on: February 22, 2020
Allogeneic and xenogeneic anti-tumor effect of callithrix jacchus natural killer cells is dependent on NKp30 and
T Müller1, L Schlahsa1, H J Zhang1
1Institute for Transfusion Medicine, Hannover Medical School, Hannover, Germany.
Abstract:
Natural Killer (NK) cells mount a fast and efficient immune response against tumor cells and are currently a major focus in the development of anti-cancer cell-based therapies. Due to major differences between the murine and human NK cell receptor system, a non-human primate model would be helpful to evaluate the efficiency of NK-cell based therapies prior to clinical applications. In humans, B7-H6 has been shown to facilitate the elimination of lymphoma cells through the interaction with its receptor NKp30. The common marmoset (Callithrix jacchus) is a new world monkey readily used in biomedical research due to its easy management and proximity to humans. In this study, we demonstrated the expression of B7-H6 antigen in marmoset B-lymphoblastoid cell lines. In addition, a method was established to isolate B- or NK-cells from peripheral blood of marmosets with purities of up to 97%We detected the expression of B7-H6 in lymphoma cells and for the first time in leukemic blasts of human acute myeloid leukemia (AML). Marmoset NK cells were shown to lyse marmoset B lymphoblastoid cell line (B-LCL) cells by up to 28.4% and human B-LCL cells by up to 20%. This effect was abrogated when the NK cells were pre-treated with an anti-NKp30 specific antibody. Also, marmoset NK cells were able to lyse primary leukemic AML cells and lymphoma cells by up to 8.3 and 20.3%respectively. Stimulation of marmoset NK cells with recombinant B7-H6 induced phosphorylation of ERK1/2 and proliferation rates. Furthermore, the secretion of IL-1β, IL-8, IFN-γ and TNF-α was significantly increased upon B7-H6 stimulation. In conclusion, we demonstrated that non-human primate NK cells have similar mechanisms for the lysis of tumor cells as human NK cells. Thus, this animal model constitutes a very promising tool for the development and evaluation of novel NK-cell based therapies.
Insights
Common marmoset Natural Killer (NK) cells show anti-tumor activity similar to human NK cells, targeting lymphoma and leukemia. This finding supports the use of marmosets as a model for developing new cancer cell therapies.
Area of Science:
- Immunology
- Oncology
- Primate Models
Background:
- Natural Killer (NK) cells are crucial for anti-tumor immunity.
- Human and murine NK cell receptor systems differ, necessitating alternative models.
- B7-H6 interaction with NKp30 is key for eliminating lymphoma cells in humans.
Purpose of the Study:
- To investigate the potential of common marmosets as a model for NK cell-based cancer therapies.
- To characterize B7-H6 expression and NK cell activity in marmosets.
- To evaluate marmoset NK cell-mediated lysis of tumor cells.
Main Methods:
- Demonstrated B7-H6 expression in marmoset B-lymphoblastoid cell lines.
- Established a method for isolating marmoset B and NK cells.
- Assessed marmoset NK cell cytotoxicity against various tumor cell lines, including human AML and lymphoma.
- Analyzed NK cell activation markers and cytokine secretion upon B7-H6 stimulation.
Main Results:
- B7-H6 expression confirmed in marmoset B-lymphoblastoid cells, human lymphoma, and AML cells.
- Marmoset NK cells effectively lysed marmoset and human B-LCL cells, as well as primary AML and lymphoma cells.
- Lysis was mediated via the NKp30 receptor and abrogated by anti-NKp30 antibody.
- B7-H6 stimulation induced NK cell proliferation, ERK1/2 phosphorylation, and secretion of key cytokines (IL-1β, IL-8, IFN-γ, TNF-α).
Conclusions:
- Marmoset NK cells exhibit anti-tumor mechanisms analogous to human NK cells.
- The common marmoset is a suitable preclinical model for evaluating NK cell-based cancer therapies.
- This model holds promise for advancing the development of novel immunotherapies.
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