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Showing 2 results for Pathogenesis

Zainab Bandalizadeh, Seyed Mojtaba Seyedmousavi, Willem J.g. Melchers, Mahmoud Fami Zaghrami, Ali Asghar Mostaed Rostami, Tahereh Shokohi,
Volume 28, Issue 163 (8-2018)
Abstract


Cryptococcosis is a serious fungal infection in both huaman and animals caused by members of the Cryptococcus neoformans/ Cryptococcus gattii species complex. The main route of entry is respiratory tract. Meningitis is the most common clinical manifestation of cryptococcosis in immunocompromised patients and considered as one of AIDS defining illnesses. The known natural sources of the fungus are avian (pigeon, chicken, and other birds) excreta, dead plants and trees like Eucalyptus, Pine, and Fig species. Cryptococcus neoformans/ Cryptococcus gattii species complex have well defined virulence factors that help them to survive and multiply in macrophages and monocytes, escape into blood and disseminate throughut the body. Laboratory diagnosis of cryptococcosis is based on direct microscopy examination, fungal isolation, serology and molecular analysis of serum and cerebrospinal fluid. Amphhotercin B combined with other antifungals including 5-flourocytosisne and fluconazole monotherapy are used for treatment of cryptococcosis. Treatment in HIV infected patients consist of three phases including induction, consolidation and maintenance therapy. The preferred therapeutic regimen is combination therapy of antifungal and highly active antiretroviral therapy. In this article,  we summarized recent studies on pathogenesis, diagnosis, and treatment of cryptococcosis in HIV infected patients.
 
Hourolein Arab, Mohammad Reza Mofid, Mahboube Rahmati, Elahe Gharehkhani, Armin Mokhtariye, Mohammad Shokrzadeh,
Volume 34, Issue 240 (12-2024)
Abstract

Autophagy is a fundamental process in eukaryotic cells, essential for maintaining cellular homeostasis and promoting survival. This process involves the formation of a structure known as the autophagosome, which sequesters damaged cellular components such as misfolded proteins and dysfunctional organelles. These components are subsequently transported to lysosomes for degradation. Autophagy allows cells to withstand various stress conditions, including nutrient deprivation, hypoxia, and microbial infections. There are three primary types of autophagy: macroautophagy, microautophagy, and chaperone-mediated autophagy, each characterized by distinct mechanisms and features.
The autophagy process is tightly regulated by autophagy-related genes (ATG) and consists of several stages: induction, autophagosome formation, fusion with lysosomes, and cargo degradation. Dysfunctional autophagy has been implicated in the development of various diseases, including cancer, neurodegenerative disorders, metabolic diseases, and bacterial or viral infections. Recent studies have highlighted the dual role of autophagy in cancer: while it can act as a tumor suppressor in early stages, it may also support tumor cell survival in advanced stages.
In the nervous system, autophagy helps prevent the accumulation of harmful proteins and supports neuronal function. Additionally, autophagy plays a significant role in combating invasive pathogens, serving as a defensive mechanism against bacteria and viruses. Research indicates that autophagy is a promising target for developing new therapeutic strategies for a wide range of diseases. In-depth investigations into the molecular pathways regulating autophagy, particularly the mTOR and AMPK pathways, offer potential avenues for innovative treatments.
This review provides a comprehensive analysis of the mechanisms and functions of autophagy, exploring its association with various human diseases. It presents a novel perspective on the potential clinical applications of autophagy, highlighting its role in the development of therapeutic strategies and deepening our understanding of this essential cellular process.


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