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Published on: February 8, 2019
HMGB-1 as a target for inflammation controlling
Jose A Nogueira-Machado1, Caroline M de Oliveira Volpe
1Núcleo de Pós Graduação e Pesquisa (NPGP), Hospital Santa Casa de Misericórdia de Belo Horizonte - Belo Horizonte-MG-Brazil. aunog.bh@terra.com.br
Recent patents offer novel strategies to control inflammation by targeting High Mobility Group Box-1 (HMGB-1). These methods aim to down-regulate HMGB-1
Area of Science:
- Immunology and Molecular Biology
- Biotechnology and Pharmaceutical Research
- Patent Law and Intellectual Property
Background:
- High Mobility Group Box-1 (HMGB-1), also known as amphoterin, is a key mediator in the pathogenesis of various inflammatory diseases.
- HMGB-1 signaling involves receptors like RAGE, TLR2, and TLR4, leading to NF-kappaB activation and pro-inflammatory responses.
- Dysregulation of HMGB-1 contributes to conditions such as sepsis, arthritis, cancer, autoimmune diseases, and diabetes.
Purpose of the Study:
- To evaluate recent patents focused on products and methods for down-regulating the pro-inflammatory actions of HMGB-1.
- To categorize and analyze different patented strategies for controlling HMGB-1 activity and its downstream inflammatory effects.
- To discuss the mechanisms, roles, and potential efficacy of these patented approaches in managing inflammation.
Main Methods:
- Systematic review and classification of patents related to HMGB-1 modulation.
- Categorization based on the mechanism of action: anti-HMGB-1 antibodies, inhibition of HMGB-1 release, competitive antagonism, RAGE-HMGB-1 signaling blockade, TLR-HMGB-1 signaling blockade, and other modulators.
- Discussion of the scientific principles and therapeutic potential of each patent group.
Main Results:
- Patents are grouped into six categories based on their distinct strategies to control HMGB-1.
- These strategies include direct neutralization, inhibition of release, receptor antagonism, and modulation of signaling pathways.
- The evaluated patents represent diverse approaches to target HMGB-1 for therapeutic benefit in inflammatory conditions.
Conclusions:
- Numerous patented technologies aim to mitigate HMGB-1-driven inflammation through various mechanisms.
- These patented approaches offer potential therapeutic avenues for a range of inflammatory and related diseases.
- Further discussion on the efficacy and clinical translation of these patented strategies is warranted.
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