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Updated: Aug 20, 2025

Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
TIM-3: a tumor-associated antigen beyond checkpoint inhibition?
Stefan Barth1,2, Krupa Naran1
1Medical Biotechnology and Immunotherapy Research Unit, Institute of Infectious Disease and Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Sabatolimab, an anti-TIM-3 antibody, offers a novel approach to cancer immunotherapy by targeting TIM-3 receptors on immune and myeloid cells. This investigational therapy shows promise for treating myeloproliferative disorders like acute myeloid leukemia.
Area of Science:
- Immunology
- Oncology
- Pharmacology
Background:
- Immune checkpoint inhibitors represent a significant advancement in cancer immunotherapy.
- TIM-3 (T-cell immunoglobulin and mucin-domain containing-3) is a receptor expressed on immune effector and myeloid cells, implicated in immune regulation.
- Myeloproliferative disorders, including acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), represent a critical area for novel therapeutic strategies.
Purpose of the Study:
- To introduce sabatolimab, a humanized anti-TIM-3 monoclonal antibody.
- To elucidate the distinct mechanisms of action of sabatolimab beyond canonical immune checkpoint inhibition.
- To highlight the potential of sabatolimab in treating myeloproliferative disorders.
Main Methods:
- Development of a high-affinity, humanized monoclonal antibody targeting TIM-3.
- Investigation of sabatolimab's effects on TIM-3 receptor and its ligands (PtdSer/galectin-9).
- Assessment of sabatolimab's impact on leukemic cell self-renewal and antibody-dependent phagocytosis.
Main Results:
- Sabatolimab targets TIM-3, a receptor on immune and myeloid cells.
- Mechanisms include blockade of TIM-3/ligand interactions, modulation of leukemic cell self-renewal, and antibody-dependent phagocytosis.
- These actions enhance the antitumor immune response through multiple pathways.
Conclusions:
- Sabatolimab represents a novel immunotherapeutic agent for myeloproliferative disorders.
- Its multi-pronged mechanism of action offers a distinct approach compared to existing immunotherapies.
- Sabatolimab holds promise as a future treatment option for hematologic malignancies.
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