Intralesional gene expression profile of JAK-STAT signaling pathway and associated cytokines in Leishmania tropica- infected patients

The JAK-STAT signaling pathway is a central cascade of signal transduction for the myriad of cytokines in which dysregulation has been implicated in progression of inflammatory and infectious diseases. However, the involvement of this pathway in human cutaneous leishmaniasis (CL) due to ( ) tropica...

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Veröffentlicht in:Frontiers in immunology 2024-09, Vol.15, p.1436029
Hauptverfasser: Hadifar, Shima, Masoudzadeh, Nasrin, Heydari, Hossein, Mashayekhi Goyonlo, Vahid, Kerachian, Mohammadali, Daneshpazhooh, Maryam, Sadeghnia, Ali, Tootoonchi, Nasim, Erfanian Salim, Reza, Rafati, Sima, Harandi, Ali M
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Sprache:eng
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Zusammenfassung:The JAK-STAT signaling pathway is a central cascade of signal transduction for the myriad of cytokines in which dysregulation has been implicated in progression of inflammatory and infectious diseases. However, the involvement of this pathway in human cutaneous leishmaniasis (CL) due to ( ) tropica warrants further investigation. This study sought to investigate differential gene expression of several cytokines and their associated genes in the lesions of -infected patients byquantitative Real-Time PCR. Further, the expression of five inhibitory immune checkpoint genes was evaluated. Results showed that the gene expression levelsof both Th1 ( , , ) and Th2 ( , ) types cytokines were increased in the lesion of studied patients. Further, elevated expression levels of , , and genes were detected in the lesions of CL patients. Notably, the expression of the majority of genes involved in JAK/STAT signaling pathway as well as checkpoint genes including , and their corresponding receptors was increased. Our finding revealed dysregulation of cytokines and related genes in the lesion of CL patients. These results highlight the need for further exploration of the functional importance of these genes in the pathogenesis of, and immunity to, CL.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2024.1436029