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Transfer of Manipulated Tumor-associated Neutrophils into Tumor-Bearing Mice to Study their Angiogenic Potential In Vivo
Published on: July 20, 2019
TNFR2 antagonist and agonist: a potential therapeutics in cancer immunotherapy
Sameer Quazi1,2,3
1GenLab Biosolutions Private Limited, Bangalore, 560043, Karnataka, India. Colonel.quazi@gmail.com.
Abstract:
Tumour necrosis factor receptor 2 or TNFR2 is considered an appealing target protein due to its limited frequency to TREGs, which are highly immunosuppressive and present on human malignancies. Numerous studies have revealed that TNFR2 is primarily found on MDSCs (myeloid-derived suppressor cells) and CD + Foxp3 + regulatory T cells (TREGs). Therefore, it has great importance in the proliferation and functional activity of TREGs and MDSCs. TNFR2 suppression must be downregulated or upregulated as required to treat malignancies and diseases like autoimmune disorders. Therefore, at the molecular level, advances in the comprehension of TNFR2's complex structure and its binding to TNF have opened the door to structure-guided drug development. Two critical obstacles to cancer treatment are the dearth of TREG-specific inhibitors and the lack of widely applicable ways to target tumours via frequently expressed surface oncogenes directly. Many researchers have discovered potential antagonists and agonists of TNFR2, which were successful in inhibiting TREGs proliferation, reducing soluble TNFR2 secretion from normal cells, and expanding T effector cells. The data represented in the following review article elucidates the clinically administrated TNFR2 antagonist and agonist in treating cancers.
Insights
Tumour necrosis factor receptor 2 (TNFR2) is a key target for cancer therapy, found on immunosuppressive cells. TNFR2 antagonists and agonists show promise in treating cancers and autoimmune disorders.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Tumour necrosis factor receptor 2 (TNFR2) is expressed on immunosuppressive cells like regulatory T cells (TREGs) and myeloid-derived suppressor cells (MDSCs).
- TNFR2 plays a crucial role in the proliferation and function of TREGs and MDSCs, making it a significant target in cancer and autoimmune diseases.
- Targeting TNFR2 offers a strategy to modulate immune responses in malignancies and autoimmune disorders.
Purpose of the Study:
- To review the role of TNFR2 in cancer and autoimmune diseases.
- To explore TNFR2 as a therapeutic target for malignancies.
- To elucidate clinically administered TNFR2 antagonists and agonists in cancer treatment.
Main Methods:
- Literature review of studies on TNFR2 expression and function.
- Analysis of TNFR2's role in TREGs and MDSCs.
- Examination of TNFR2 antagonists and agonists in preclinical and clinical settings.
Main Results:
- TNFR2 is highly expressed on immunosuppressive TREGs and MDSCs, crucial for their activity.
- TNFR2 modulation is vital for treating cancers and autoimmune disorders.
- Development of TNFR2 antagonists and agonists has shown success in inhibiting TREG proliferation and enhancing T effector cells.
Conclusions:
- TNFR2 is a promising therapeutic target for cancer treatment.
- Structure-guided drug development for TNFR2 holds potential for novel cancer therapies.
- TNFR2 antagonists and agonists are being investigated for clinical application in treating cancers.
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