Dendritic Cells: The Long and Evolving Road towards Successful Targetability in Cancer
Enrica Marmonti1, Jacqueline Oliva-Ramirez1, Cara Haymaker1
1Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Abstract:
Dendritic cells (DCs) are a unique myeloid cell lineage that play a central role in the priming of the adaptive immune response. As such, they are an attractive target for immune oncology based therapeutic approaches. However, targeting these cells has proven challenging with many studies proving inconclusive or of no benefit in a clinical trial setting. In this review, we highlight the known and unknown about this rare but powerful immune cell. As technologies have expanded our understanding of the complexity of DC development, subsets and response features, we are now left to apply this knowledge to the design of new therapeutic strategies in cancer. We propose that utilization of these technologies through a multiomics approach will allow for an improved directed targeting of DCs in a clinical trial setting. In addition, the DC research community should consider a consensus on subset nomenclature to distinguish new subsets from functional or phenotypic changes in response to their environment.
Insights
Dendritic cells (DCs) are crucial for adaptive immunity and cancer therapies. New multiomics technologies can improve DC targeting, but standardized nomenclature is needed for better clinical trial outcomes.
Area of Science:
- Immunology
- Cancer Biology
- Cellular Therapy
Background:
- Dendritic cells (DCs) are key myeloid cells initiating adaptive immune responses.
- DCs are promising targets for cancer immunotherapy, but clinical translation remains challenging.
- Existing research presents complexities in DC development, subsets, and functional responses.
Purpose of the Study:
- To review current knowledge and challenges in targeting dendritic cells for cancer therapy.
- To propose advanced technological approaches for improved DC-directed cancer treatments.
- To advocate for standardized nomenclature for dendritic cell subsets.
Main Methods:
- Literature review of dendritic cell biology and therapeutic targeting.
- Analysis of emerging technologies, including multiomics approaches.
- Discussion of challenges in clinical trial design and interpretation.
Main Results:
- Despite their importance, effective clinical targeting of DCs in cancer has yielded limited success.
- Technological advancements offer new possibilities for understanding and manipulating DCs.
- A lack of standardized nomenclature complicates the identification and characterization of DC subsets.
Conclusions:
- Multiomics approaches are essential for advancing the directed targeting of dendritic cells in clinical settings.
- Standardized nomenclature is crucial for distinguishing distinct DC subsets and their functions.
- Future cancer immunotherapies may benefit from refined strategies based on a deeper understanding of DCs.
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