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Orthotopic Implantation and Peripheral Immune Cell Monitoring in the II-45 Syngeneic Rat Mesothelioma Model
Published on: October 2, 2015
Osteogenic sarcoma. Immunologic parameters before and during immunotherapy with tumor-specific transfer factor.
The Journal of Clinical Investigation
|March 1, 1975
Summary
Osteogenic sarcoma patients receiving tumor-specific transfer factor showed increased cell-mediated cytotoxicity. Measurements of cell-mediated cytotoxicity help monitor therapy effectiveness and select transfer factor donors.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Osteogenic sarcoma is a challenging bone cancer.
- Cell-mediated cytotoxicity plays a role in anti-tumor immunity.
- Transfer factor therapy is being explored for various conditions.
Purpose of the Study:
- To evaluate the effect of tumor-specific transfer factor on cell-mediated cytotoxicity in osteogenic sarcoma patients.
- To assess the utility of serial cytotoxicity measurements in monitoring treatment efficacy.
Main Methods:
- Serial in vitro measurements of tumor-specific cell-mediated cytotoxicity and T-cell subsets (active and total rosette-forming cells).
- Administration of osteogenic sarcoma-specific or non-specific dialyzable transfer factor to patients.
- Correlation of cytotoxicity levels with tumor burden and treatment response.
Main Results:
- Patients with large tumors had low baseline cytotoxicity, which increased after tumor-specific transfer factor administration.
- Tumor-specific transfer factor increased cell-mediated cytotoxicity in all treated patients.
- Non-specific transfer factor was associated with declining cytotoxicity.
- Clinical and histological changes (pain, edema, lymphocytic infiltrates) suggested anti-tumor response in some patients.
Conclusions:
- Tumor-specific transfer factor may enhance cell-mediated cytotoxicity against osteogenic sarcoma.
- Serial cell-mediated cytotoxicity measurements are valuable for monitoring transfer factor therapy efficacy.
- Cytotoxicity measurements can guide the selection of optimal donors for tumor-specific transfer factor.

