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Targeting ILT4 to Improve Immunotherapy Efficacy in Solid Tumour: From Bench to Bedside
Aiqin Gao1, Shuyun Wang2, Yuping Sun2
1Department of Thoracic Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.
Immunoglobulin-like transcript 4 (ILT4) blockade emerges as a promising strategy to overcome resistance to cancer immunotherapy. Targeting ILT4 in the tumor microenvironment can enhance T-cell function and improve treatment efficacy.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy but show limited efficacy in solid tumors.
- The immunosuppressive tumor microenvironment (TME) hinders ICI effectiveness, necessitating novel therapeutic targets.
- Immunoglobulin-like transcript 4 (ILT4) is an inhibitory molecule implicated in tumor growth, metastasis, and immune evasion.
Purpose of the Study:
- To review recent advances in understanding ILT4 function within the TME.
- To summarize translational research on therapeutic ILT4 antibodies.
- To highlight clinical data on ILT4 blockade for enhancing immunotherapy.
Main Methods:
- Literature review of ILT4 research.
- Analysis of translational studies on ILT4 antibodies.
- Summary of emerging clinical trial data.
Main Results:
- ILT4 is expressed in tumor cells and immune cells within the TME, promoting tumor progression.
- Therapeutic antibodies targeting ILT4 are under development.
- Early clinical data suggest ILT4 blockade can improve immunotherapy response.
Conclusions:
- ILT4 represents a novel immunotherapeutic target for overcoming resistance to current cancer treatments.
- ILT4 blockade holds potential for combination therapies to enhance anti-tumor immunity.
- Further clinical investigation of ILT4-targeting agents is warranted.
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