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Isolation Protocol of Mouse Monocyte-derived Dendritic Cells and Their Subsequent In Vitro Activation with Tumor Immune Complexes
Published on: May 31, 2018
Immunologic monitoring of cellular responses by dendritic/tumor cell fusion vaccines
Shigeo Koido1, Sadamu Homma, Akitaka Takahara
1Division of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan. shigeo_koido@jikei.ac.jp
Abstract:
Although dendritic cell (DC)- based cancer vaccines induce effective antitumor activities in murine models, only limited therapeutic results have been obtained in clinical trials. As cancer vaccines induce antitumor activities by eliciting or modifying immune responses in patients with cancer, the Response Evaluation Criteria in Solid Tumors (RECIST) and WHO criteria, designed to detect early effects of cytotoxic chemotherapy in solid tumors, may not provide a complete assessment of cancer vaccines. The problem may, in part, be resolved by carrying out immunologic cellular monitoring, which is one prerequisite for rational development of cancer vaccines. In this review, we will discuss immunologic monitoring of cellular responses for the evaluation of cancer vaccines including fusions of DC and whole tumor cell.
Insights
Dendritic cell (DC)-based cancer vaccines show promise in preclinical studies but limited clinical success. Evaluating these vaccines requires immunologic monitoring beyond standard tumor response criteria.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Dendritic cell (DC)-based cancer vaccines demonstrate potent antitumor activity in preclinical models.
- Clinical translation of DC-based cancer vaccines has yielded limited therapeutic success.
- Current RECIST and WHO criteria may not fully capture the immune-mediated effects of cancer vaccines.
Purpose of the Study:
- To review immunologic monitoring strategies for evaluating cancer vaccines.
- To highlight the limitations of standard tumor response criteria for assessing vaccine efficacy.
- To discuss the role of cellular immune monitoring in the rational development of DC-based cancer vaccines.
Main Methods:
- Review of existing literature on cancer vaccine evaluation.
- Discussion of immunologic monitoring techniques for cellular responses.
- Analysis of the applicability of RECIST and WHO criteria to cancer vaccines.
Main Results:
- Standard tumor response criteria may not adequately assess cancer vaccine efficacy.
- Immunologic monitoring of cellular responses is crucial for vaccine development.
- DC-DC fusions and whole tumor cell vaccines require specific evaluation methods.
Conclusions:
- Rethinking evaluation metrics is necessary for advancing cancer vaccine therapy.
- Integrating immunologic monitoring with clinical assessment will improve vaccine development.
- Cellular immune monitoring is essential for understanding and optimizing cancer vaccine outcomes.
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