Publications by authors named "Amin Moradi Hasan-Abad"

Inflammation is a defensive mechanism that safeguards the human body against detrimental stimuli. Within this intricate process, ADAM17, a zinc-dependent metalloprotease, emerges as an indispensable element, fostering the activation of diverse inflammatory and growth factors within the organism. Nonetheless, ADAM17 malfunctions can augment the rate of growth, inflammatory factors, and subsequent damage.

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Breast cancer is a common form of cancer among women characterized by the growth of malignant cells in the breast tissue. The most common treatments for this condition include chemotherapy, surgical intervention, radiation therapy, hormone therapy, and biological therapy. The primary issues associated with chemotherapy and radiation therapy are their adverse events and significant financial burden among patients in underdeveloped countries.

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The result of infection of bone with microorganisms is osteomyelitis and septic arthritis. Methicillin-resistant (MRSA) is responsible for most of its cases (more than 50%). Since MRSA is resistant to many treatments, it is accompanied by high costs and numerous complications, necessitating more effective new treatments.

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Immunosuppressive agents are routinely used to control autoimmunity. However, some adverse events are correlated to their clinical applications. The aim of this study was to study the clinical findings and ocular and cutaneous side effects of chloroquine (CQ) and hydroxychloroquine (HCQ), as current immunomodulators, in patients with rheumatoid arthritis (RA) and systemic lupus erythematosus (SLE).

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This mini-review analyzed two approaches to screening bacterial contamination and utilizing pathogen reduction technology (PRT) for Platelet concentrates (PCs). While the culture-based method is still considered the gold standard for detecting bacterial contamination in PCs, efforts in the past two decades to minimize transfusion-transmitted bacterial infections (TTBIs) have been insufficient to eliminate this infectious threat. PRTs have emerged as a crucial tool to enhance safety and mitigate these risks.

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  • Pancreatic ductal adenocarcinoma (PDAC) is a type of cancer that is very hard to treat and often not found until it's too late, leading to a low survival rate.
  • There are no good treatments for this cancer, and most patients can't respond well to chemotherapy, which makes it difficult to manage.
  • Researchers are studying special kinds of molecules called non-coding RNAs (ncRNAs) to see how they can help in finding this cancer earlier and developing better treatments for people with PDAC.
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Recent studies have proposed various COVID-19 vaccines to control the disease and protect susceptible individuals. However, immunogenicity and safety of COVID-19 vaccines in various populations are not well identified yet. Therefore, this study aimed to elucidate the efficacy and safety of the BBIBP-CorV (Sinopharm) and ChAdOx1 nCoV-19 (Oxford-AstraZeneca) vaccines in healthy subjects and patients with autoimmune diseases.

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  • * This presentation will specifically examine the characteristics and catalytic activities of peroxidase-like nanozymes, discussing their role in cancer diagnosis and treatment through various therapy methods.
  • * The goal is to provide insights that could lead to the development of new anticancer therapies using nanozymes, ultimately contributing to effective tumor treatment strategies.
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  • Nanotechnology emerged in the 1980s, enabling scientists to manipulate matter at the nanoscale, which has led to significant advancements in targeting biomolecular interactions for medical applications.
  • The combination of bio- and nanotechnologies is transforming disease detection, treatment, and management, with emerging uses in antibiotic resistance, cancer therapies, and neurodegenerative disorders.
  • Recent developments include smart nanostructured materials for regenerative medicine and immunotherapy, highlighting the potential for groundbreaking advancements in delivering therapies and vaccines.
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Polymorphism in human platelet antigen (HPA)-1 and HPA-3 (GPIIb/IIIa), HPA-2 (GPIb/IX), HPA-4 (GPIIIa), HPA-5 (GPIa/IIa), & HPA-15 (CD109) was investigated in 86 COVID-19-infected patients with thrombocytopenia (Group A) and 136 COVID-19-infected patients without thrombocytopenia (Group B). HPA genotyping was done by the sequence-specific primers PCR method. Lower HPA-3a and higher HPA-3b ( = 0.

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Nanoparticles have demonstrated noteworthy advancements in the management of various complex medical conditions, particularly cancer. In any case, these particles still harbor the potential to improve medicate conveyance to challenging, hard-to-reach loci. The interactions that occur between nanoparticles and red blood cells during their journey throughout the human body, despite exposure to blood, are still not fully understood.

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Objectives: Immunotherapy has changed the landscape of oncology over the last decade and has become a standard of care for various cancers. Researchers previously demonstrated that B16-F10 melanoma in C57Bl6 mice is resistant to immune checkpoint inhibitors. The goal of this study was to investigate how anti-PD1 antibodies functioned in combination with a new antimicrobial peptide (AMP) called moronecidin-like peptide (MLP).

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Pancreatic cancer is one of the highly invasive and the seventh most common cause of death among cancers worldwide. To identify essential genes and the involved mechanisms in pancreatic cancer, we used bioinformatics analysis to identify potential biomarkers for pancreatic cancer management. Gene expression profiles of pancreatic cancer patients and normal tissues were screened and downloaded from The Cancer Genome Atlas (TCGA) bioinformatics database.

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  • Vaccination is crucial for controlling the COVID-19 pandemic and protecting vulnerable groups, especially those with autoimmune inflammatory rheumatic diseases (AIIRD) who are prioritized for receiving the BBIBP-CorV vaccine.
  • The study involved 200 participants (100 healthy controls and 100 AIIRD patients) and assessed antibody levels and adverse events before and after vaccination, revealing that AIIRD patients had significantly lower antibody responses than healthy controls.
  • Despite a lower antibody response, both groups reported similar side effects from the vaccine, and previous COVID-19 infection was linked to higher neutralizing antibody levels in vaccinated subjects.
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Type I hypersensitivity (allergic reaction) is an unsuitable or overreactive immune response to an allergen due to cross-link immunoglobulin E (IgE) antibodies bound to its high-affinity IgE receptors (FcεRIs) on effector cells. It is needless to say that at least two epitopes on allergens are required to the successful and effective cross-linking. There are some reports pointing to small proteins with only one IgE epitope could cross-link FcεRI-bound IgE through homo-oligomerization which provides two same IgE epitopes.

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  • Gynecologic cancer is a leading cause of death among women, driven by changes in specific genes that influence tumor development and treatment resistance.
  • Recent research emphasizes the importance of detecting molecular changes in oncogenes and tumor suppressor genes for early diagnosis and personalized treatment.
  • The study highlights cancer stem cells (CSCs) as key players in cancer progression and recurrence, aiming to improve understanding of their molecular mechanisms to develop more effective therapies.
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  • Interferonbeta-1b (IFNβ-1b) is a therapeutic protein for treating multiple sclerosis, but long-term use can lead to the development of anti-drug antibodies (ADAs) that reduce its effectiveness.
  • This study aimed to use bioinformatics and genetic engineering to predict and modify T-cell epitopes in IFNβ-1b to reduce immunogenicity.
  • The research successfully created mutant proteins with maintained biological activity comparable to Betaseron, showing a significant reduction in antibody response by about 50% for certain engineered variants.
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  • Cancer immunotherapy uses the immune system to attack cancer cells, with IL-2 being a key factor that enhances immune functions but is limited by its short serum half-life, leading to high-dose administration and side effects.
  • Researchers developed a fusion protein called ABD-rIL-2 that binds to serum albumin, which improves the serum half-life of IL-2, making it more effective and reducing the need for repeated high doses.
  • In tests with mice, the ABD-rIL-2 fusion protein maintained its bioactivity while demonstrating a significantly longer serum half-life compared to standard rIL-2, suggesting a promising alternative for cancer treatment.
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Interferon β (IFNβ) is the most prescribed drug that has been used frequently for the treatment of multiple sclerosis (MS) patients. The aim of this study is to improve the production of IFNβ by induction of site directed mutagenesis. Accordingly, recombinant constructs were designed in order to enhance the expression of IFNβ mRNA and protein.

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