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Human β-defensin 1 update: Potential clinical applications of the restless warrior
Ángel H Álvarez1, Moisés Martínez Velázquez1, Ernesto Prado Montes de Oca1
1Personalized Medicine National Laboratory (LAMPER), Medical and Pharmaceutical Biotechnology Unit, Research Center of Technology and Design Assistance of Jalisco State (CIATEJ), National Council of Science and Technology (CONACYT), Av. Normalistas 800, Col. Colinas de la Normal, Guadalajara, Mexico.
Abstract:
Human β-defensin 1 (hBD-1) is a multifaceted antimicrobial peptide being a tumour suppressor and, depending on call of duty, capable of inducing self-nets and neutrophil extracellular traps (NETs) to capture and/or kill bacteria, participates in inflammatory responses in chronic diseases including hBD-3 upregulation and also capable of up/downregulation in the presence of certain species of Lactobacillus sp. Thus, is regulated by host microbiota. Alleles, genotypes and/or altered gene expression of its coding gene, DEFB1, have been associated with several human diseases/conditions ranging from metabolic/chronic (e.g. cancer), infectious (e.g. tuberculosis, HIV/AIDS), inflammatory (gastrointestinal diseases), male infertility and more recently, neurologic (e.g. depression and Alzheimer) and autoimmune diseases (e.g. vitiligo and systemic lupus erythematosus). The present update focuses on novel DEFB1/hBD-1 properties and biomarker features, its biological function and the pharmaceutical potential uses of antimicrobial peptide elicitors (APEs) or the engineered peptide in the treatment of hBD-1-related human diseases.
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