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Arash Babaei

Arash Babaei

Academic rank: Assistant Professor
ORCID:
Education: PhD.
ScopusId:
HIndex:
Faculty: science
Address: Head of International Relations Bureau and Foreign students’ affairs of Malayer University international@malayeru.ac.ir Tel & FAX for secretary: +98(81) 32355416 PhD in Microbiology & Biotechnology Department of Biology, Faculty of Sciences, Malayer University, Malayer, Iran Postcode: 65719-95863 IRAN Mobil Number.: +98(918) 8512622 a.babaei@malayeru.ac.ir
Phone: 00989188512622

Research

Title
Restricted leptin antagonism as a therapeutic approach to treatment of autoimmune diseases
Type
JournalPaper
Keywords
Adipocyte hormone, Antagonism, Autoimmune disease, Immune response, Leptin
Year
2011
Journal Hormones-International Journal of Endocrinology and Metabolism
DOI
Researchers Arash Babaei

Abstract

Leptin, the adipocyte derived hormone, has a pivotal role in regulating energy homeostasis and appetite. Beyond this essential role in bodyweight control, leptin also regulates the immune responses. Leptin has pro-inflammatory effects on T cell populations, shifting the T helper balance towards a TH1 phenotype, through induction of pro-inflammatory cytokines and stimulation of macrophage and natural killer cell function. Acute starvation reduces serum leptin levels, resulting in an impaired cellular immune response. The TH1 pro-inflammatory immune response, a homeostatic response mediated by the low leptin levels, is also impaired during starvation. Leptin-deficient or leptin receptor mutant mice are protected against the development of several inflammatory or various T cell-dependent autoimmune diseases. Therefore, leptin appears to have a central role in the immune response and low leptin levels may protect against autoimmune disease. Here we review the role of leptin in the immune responses, with emphasis on autoimmune diseases. We will also discuss the application of leptin antagonist therapy for prevention and treatment of immunity related disorders.