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Neutrophil Isolation and Analysis to Determine their Role in Lymphoma Cell Sensitivity to Therapeutic Agents
Published on: March 25, 2016
Microenvironment Cell Contribution to Lymphoma Immunity
1Departments of Pathology & Laboratory Medicine, Yale University School of Medicine, New Haven, CT, United States.
Insights
This review details the cellular components of the lymphoma microenvironment and their roles in immunity during immunotherapy. Understanding these interactions is key to developing new lymphoma treatments and overcoming resistance.
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- The lymphoma microenvironment is a complex milieu of cellular and non-cellular components.
- These components, including immune cells, stromal cells, and exosomes, significantly influence tumor progression and immune response.
Purpose of the Study:
- To review the functions, localization, and interactions of cellular players within the lymphoma microenvironment.
- To summarize their contribution to lymphoma immunity, particularly in the context of immunotherapy.
Main Methods:
- Systematic literature search of PubMed.
- Careful evaluation of primary literature for replicability.
Main Results:
- Detailed description of key cellular components: mesenchymal stem/stromal cells (MSCs), lymphoma-associated macrophages (LAMs), dendritic cells, cytotoxic T cells, PD-1+ CD4+ tumor infiltrating lymphocytes (TILs), exhausted T-cells (TIM-3+, LAG-3+), regulatory T cells, and natural killer cells.
- Overview of lymphoma exosomes and their dual role in anti-tumor effects and immune dysfunction.
Conclusions:
- Understanding the lymphoma microenvironment's cellular dynamics is critical for developing novel therapeutics.
- This knowledge is essential for blocking immune escape, promoting tumor surveillance, and addressing immunotherapy resistance and adverse events.
Abstract:
Lymphoma microenvironment is a complex system composed of stromal cells, blood vessels, immune cells as well as extracellular matrix, cytokines, exosomes, and chemokines. In this review, we describe the function, localization, and interactions between various cellular components. We also summarize their contribution to lymphoma immunity in the era of immunotherapy. Publications were identified from searching Pubmed. Primary literature was carefully evaluated for replicability before incorporating into the review. We describe the roles of mesenchymal stem/stromal cells (MSCs), lymphoma-associated macrophages (LAMs), dendritic cells, cytotoxic T cells, PD-1 expressing CD4+ tumor infiltrating lymphocytes (TILs), T-cells expressing markers of exhaustion such as TIM-3 and LAG-3, regulatory T cells, and natural killer cells. While it is not in itself a cell, we also include a brief overview of the lymphoma exosome and how it contributes to anti-tumor effect as well as immune dysfunction. Understanding the cellular players that comprise the lymphoma microenvironment is critical to developing novel therapeutics that can help block the signals for immune escape and promote tumor surveillance. It may also be the key to understanding mechanisms of resistance to immune checkpoint blockade and immune-related adverse events due to certain types of immunotherapy.
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