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عضویت

جستجوی مقالات مرتبط با کلیدواژه « Immunomodulatory Effects » در نشریات گروه « پزشکی »

  • Tahereh Jamali, Susan Kaboudanian Ardestani *
    Background

    Cancer therapy necessitates innovative approaches with enhanced efficacy and reduced side effects. Essential oils have gained attention because of their diverse biological properties and relatively low toxicity. Zataria multiflora essential oil (ZEO) and Oliveria decumbens essential oil (OEO) exhibit promising anti-cancer effects, particularly in modifying oxidative stress and inflammation. Both oils boast complex compositions rich in bioactive compounds, including oxygenated monoterpenes and phenolic compounds like carvacrol and thymol. Hence, this study investigates essential oils’ anti-cancer, anti-oxidant and immunomodulatory effects, focusing on ZEO and OEO.

    Materials and Methods

    This review briefly considers the intricate mechanisms of several essential oils, encompassing anti-oxidant, anti-inflammatory and anti-cancer properties. Then the review delves into the multifaceted mechanisms underlying the anti-cancer properties of ZEO and OEO. 

    Results

    Studies showcase the ability of ZEO and OEO to induce apoptosis in cancer cells through various pathways, such as mitochondrial dysfunction, reactive oxygen species (ROS) generation and DNA damage while sparing normal cells. Our studies further validated the immunomodulatory effects of OEO and ZEO in tumor-bearing mice, resulting in reduced tumor volume. Additionally, this review confirmed the synergistic effect of ZEO when combined with doxorubicin to inhibit cancer cells. 

    Conclusion

    Some essential oils, such as ZEO and OEO, present promising natural compounds in cancer therapy, offering diverse mechanisms of action targeting various aspects of tumor biology.

    Keywords: Essential Oil, Zataria Multiflora, Oliveria Decumbens, Immunomodulatory Effects, Anti-Cancer Effects}
  • Jamal Motallebzadeh Khanmiri, Mohammad Khani Eshratabdi, Amirreza Nasirzadeh, Mahdie Nematzade, Amir Talebpour, Seyed Hadi Mousavi

    The SARS-CoV-2 virus is a member of the coronavirus family that caused the COVID-19 respiratory disease epidemic in China before the global pandemic of the disease in late 2019. The virus's genome is of 79% similarity to that of the SARS-CoV virus, using the ACE2 receptor to enter its target cells. The most common symptoms of this disease include fever, cough, pulmonary involvement, and sometimes gastrointestinal symptoms. A decline in both the number and function of lymphocytes and a severe increase in leukocyte inflammatory activity are among the most obvious immunological complications of this disease. If the immune system response to the virus is inadequate, the disease can become acute. Immune cells activity leads to a sharp increase in the number of blood cytokines, causing "cytokine storm," which in turn can cause systematic damages to the heart, lungs, and kidneys, and ultimately may lead to death. Mesenchymal stem cell therapy offers a promising approach to reducing the destructive impacts of infection in patients with COVID-19. Mesenchymal stem cells can secrete immune-modulating factors that suppress cytokine storms. Furthermore, the role of mesenchymal stem cells in preventing cell death and inhibiting tissue fibrosis has been well demonstrated. This review shows available clinical trials that have tapped into the therapeutic potential of the umbilical cord mesenchymal stem cells in patients with COVID-19.

    Keywords: Umbilical Cord, Mesenchymal Stem Cell, COVID-19, SARS-CoV-2, Immunomodulatory Effects, Clinical Trial}
  • Evgenii Plotnikov *, Elena Korotkova, Olesya Voronova, Elena Dorozhko, Nikolay Bohan, Sergey Plotnikov
    Introduction
    Lithium salts are known as effective psychotropic medicine for treatment bipolar disorder and may be used to treat alcoholism, schizoaffective disorders, and cluster headaches. The antioxidant activity and immunomodulatory effects of prospective lithium compounds have been investigated in this work.
    Materials And Methods
    The antioxidant properties were studied by the voltammetry method. Influence of the lithium compounds on the immune cells of human blood were determined by measuring phagocytic activity of leucocytes and by the rate of blastic transformation of lymphocytes.
    Results
    Relatively better antioxidant and immunotropic properties have been revealed for lithium ascorbate, compare to widely used drug-lithium carbonate. Lithium aspartate revealed antioxidant activity, as well.
    Conclusion
    Studied lithium salts can be considered as prospective psychotropic antioxidant with immunomodulatory effects. The combination of these properties significantly extends the potential medical applications of lithium salts.
    Keywords: antioxidant activity, immunomodulatory effects, voltammetry, lithium ascorbate, lithium aspartate}
  • محمدحسین کریمی، عزیز ژاپونی، منوچهر رسولی*، سلیمه ابراهیم نژاد
    زمینه و هدف
    با توجه به نقش کلیدی سلول دندریتیک در ایجاد پاسخ سیستم ایمنی بر علیه آنتی ژن های میکروبی و بیماری ها، در این مطالعه اثر پروتئین نوترکیب اگزوتوکسین A باکتری پسودوموناس آئروژینوزا در بلو غ و فعال سازی سلول های دندریتیک مورد بررسی قرار گرفت.
    مواد و روش ها
    با استفاده از DNA باکتری پسودوموناس آئروژینوزا پروتئین نوترکیب اگزوتوکسین A ساخته شد و اثر سیتوتوکسیک آن بر سلول دندریتیک به وسیله تست MTT مورد مطالعه قرار گرفت. همچنین اثر این آنتی ژن بر بیان مولکول های CD40، CD86 و MHCΠ بر روی سلول های دندریتیک با استفاده از تکنیک فلوسایتومتری مورد بررسی قرار گرفت. علاوه بر این ها اثر این آنتی ژن بر تکثیر سلول T به وسیله واکنش مختلط لنفوسیتی (MLR) و ترشح سایتوکاین های IL-4 و IFN-γ بررسی شد. همچنین اثر این آنتی ژن بر تولید IL-12 توسط سلول های دندریتیک به کمک تکنیک ELISA بررسی شد. نتایج حاصل به وسیله تست آماری one way ANOVA مورد بررسی قرار گرفت.
    نتایج
    اگزوتوکسین A بقاء سلول دندریتیک را کاهش نداد و همچنین میزان بیان مولکول های کمک تحریکی CD40، CD86 و MHCΠنسبت به کنترل منفی تغییر معنی داری پیدا نکرد. این آنتی ژن میزان تکثیر سلول T را کاهش داد و این کاهش تکثیر در غلظت 0/1 معنی دار بود. میزان ترشح IL-12 توسط سلول دندریتیک تحت تاثیر این آنتی ژن افزایش یافت ولی میزان ترشح IL-4 و IFN-γ در تستMLR کاهش معنی داری را نشان نداد.
    نتیجه گیری
    این آنتی ژن باعث تغییر در ترشح سایتوکاین ها توسط سلول های ایمنی شده و تکثیر سلول های T را کاهش می دهد.
    کلید واژگان: اگزوتوکسین A, سلول دندریتیک, اثرات ایمونومدولاتوری}
    Mohammad Hossein Karimi, Aziz Japoni, Manouchehr Rasouli *, Salimeh Ebrahimnezhad
    Background and Objective
    Dendritic cell (DC) is as a key cell in activation of immune response against microbes and disease. Therefore, the effect of recombinant exotoxin A of Pseudomonas aeruginosa on the maturity and the activation of DCs was evaluated in this study.
    Materials and Methods
    Recombinant exotoxin A was produced from Pseudomonas aeruginosa DNA. MTT assay was used to evaluate the cytotoxicity of this protein on DCs. The expression of co-stimulatory molecules CD40, CD86, and MHCΠ was evaluated by flow cytometry. Moreover, the effect of this antigen (Ag) on T-cell proliferation was evaluated using Mixed Lymphocyte Reaction (MLR) assay and the secretion of IL-4 and IFN- γ. Secretion of IL-12 by DCs was measured with Enzyme-Linked Immunosorbent Assay (ELISA) method. The data were collected and analyzed with one way ANOVA test.
    Results
    Recombinant exotoxin A had no effect on DCs viability. In addition, expression of CD40, CD86, and MHCΠ did not change significantly compared to the negative control cells. Moreover, T-cells proliferation was decreased significantly at the concentration of 0.1µg/ml of this Ag. The secretion of IL-12 was increased by DCs, in contrast the secretion of IL-4 and IFN-γ in MLR supernatant did not decrease significantly.
    Conclusion
    Exotoxin A decreases the proliferation of T-cells and also leads to a change in the pattern of cytokine secretion of immune cells.
    Keywords: Exotoxin A, Dendritic cell, Immunomodulatory effects}
نکته
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