<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Allergy, Asthma and Immunology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Scales of Magt1 Gene: Novel Mutations, Different Presentations</title>
    <FirstPage>92</FirstPage>
    <LastPage>97</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Sule</FirstName>
        <LastName>Haskologlu</LastName>
        <affiliation locale="en_US">Department of Pediatric, Immunology and Allergy and Hematopoietic Stem Cell Transplantation Unit, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Kubra</FirstName>
        <LastName>Baskin</LastName>
        <affiliation locale="en_US">Department of Pediatric, Immunology and Allergy and Hematopoietic Stem Cell Transplantation Unit, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Caner</FirstName>
        <LastName>Aytekin</LastName>
        <affiliation locale="en_US">Pediatric Immunology Clinic, Dr. Sami Ulus Obstetrics and Gynecology and Pediatric Health and Diseases, Training and Research Hospital, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Candan</FirstName>
        <LastName>Islamoglu</LastName>
        <affiliation locale="en_US">Department of Pediatric, Immunology and Allergy and Hematopoietic Stem Cell Transplantation Unit, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Serdar</FirstName>
        <LastName>Ceylaner</LastName>
        <affiliation locale="en_US">Intergen Genetic Diagnostics Center, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Figen</FirstName>
        <LastName>Dogu</LastName>
        <affiliation locale="en_US">Department of Pediatric, Immunology and Allergy and Hematopoietic Stem Cell Transplantation Unit, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Nurdan</FirstName>
        <LastName>Tacyildiz</LastName>
        <affiliation locale="en_US">Department of Pediatric, Hematology and Oncology, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Emel</FirstName>
        <LastName>Unal</LastName>
        <affiliation locale="en_US">Department of Pediatric, Hematology and Oncology, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Aydan</FirstName>
        <LastName>Ikinciogullari</LastName>
        <affiliation locale="en_US">Department of Pediatric, Immunology and Allergy and Hematopoietic Stem Cell Transplantation Unit, School of Medicine, Ankara University, Ankara, Turkey</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>02</Month>
        <Day>02</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>07</Month>
        <Day>24</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Loss-of-function mutations in magnesium transporter 1 (MAGT1) gene cause X-linked magnesium deficiency with Epstein&#x2013;Barr virus (EBV) infection and neoplasm (X-MEN), a disease with quite diverse clinical and immunological consequences. The phenotypic characteristics of the initially described patients included CD4+ T cell lymphopenia, immune deficiency, EBV viremia, and EBV-related lymphoproliferative disease. To date, a total of 25 patients have been reported. The spectrum of the MAGT1 defect ranges from other viral infections (HSV, VZV, CMV, MCV) and sinopulmonary bacterial infections, autoimmune diseases, non-EBV driven lymphoproliferative disease, Castleman disease, HHV8+ Kaposi's sarcoma, vasculitis (Kawasaki) to glycosylation defects in new patients. Here, we report 2 patients from two different families with novel MAGT1 mutations and different clinical features. The first patient presented with B cell lymphoma and low IgM level without recurrent infections. The second patient presented with recurrent upper respiratory tract infections, Kawasaki-like disease, hypogammaglobulinemia, and T cell lymphopenia. X-MEN disease is the first phenotype identified due to MAGT1 mutation. The identification of new mutations and atypical presentations will clarify whether there is a relationship between the genotype and the phenotype and the characteristics of the disease.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3111</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3111/1798</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Gut Microbiota Modulates the Efficiency of Programmed Cell Death Protein 1 Cancer Immunotherapies</title>
    <FirstPage>1</FirstPage>
    <LastPage>11</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Azam</FirstName>
        <LastName>Samei</LastName>
        <affiliation locale="en_US">Department of Clinical Laboratory Sciences, School of Allied Medical Sciences, Kashan University of Medical Sciences, Kashan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mostafa</FirstName>
        <LastName>Khedri</LastName>
        <affiliation locale="en_US">Department of Clinical Laboratory Sciences, School of Allied Medical Sciences, Kashan University of Medical Sciences, Kashan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>10</Month>
        <Day>13</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>08</Month>
        <Day>02</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Program cell death protein 1 (PD1) is considered as an inhibitory molecule that is expressed on the surface of activated T-cells and bound to PD-L1 and PD-L2 ligands. Several types of cancer cells express PD-L1 which can bind to PD1 on the surface of tumor-specific T-cells. PD1/PD-L1 ligation triggers a pathway to protect tumor cells from an effective response of tumor-specific T-cells. Different PD1/PD-L1 blocker antibodies are clinically used to promote the T-cell response against the cancer cells. Current studies suggest that the gut microbiome impacts the efficiency of PD1 blockade therapy in cancer patients. The association of several bacterial species with PD1 responder patients has been determined. The present study reviewed previous reports on the relation between the microbiome and immune checkpoint therapy (ICT). The results of studies were discussed considering adjuvant and molecular mimicry of microbial antigens by tumor-associated antigens and metabolic effects of microbial products on ICT.
&#xD;

&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3003</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3003/1787</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The Association between Proportion HLA-BW4 or HLA-BW6 May Causes Immunity Failure in COVID-19</title>
    <FirstPage>101</FirstPage>
    <LastPage>103</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Hamid</FirstName>
        <LastName>Chegni</LastName>
        <affiliation locale="en_US">Department of Laboratory Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ardeshir</FirstName>
        <LastName>Abbasi</LastName>
        <affiliation locale="en_US">Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hajar</FirstName>
        <LastName>Rajayi</LastName>
        <affiliation locale="en_US">Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zuhair</FirstName>
        <LastName>Mohammad Hassan</LastName>
        <affiliation locale="en_US">Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>05</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>30</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">No Abstract&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2844</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/2844/1800</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Identification of the Most Common Allergens of Acer velutinum Pollen</title>
    <FirstPage>81</FirstPage>
    <LastPage>85</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Najmeh</FirstName>
        <LastName>Sepahi</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Soheila</FirstName>
        <LastName>Alyasin</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran AND Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Kanannejad</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Esmaeilzadeh</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran AND Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Farzaneh</FirstName>
        <LastName>Mohammadalizadeh Shirazi</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Babaei</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shirin</FirstName>
        <LastName>Farjadian</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran AND Department of Immunology, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>27</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>10</Month>
        <Day>10</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Pollens have been identified as potent inducers of allergic diseases worldwide. Acer velutinum (Persian maple) tree is an important source of allergic pollens in Iran. This study aimed to identify the immunoglobulin E (IgE)-reactive components of A. velutinum pollen extract in patients with maple allergy. We aimed to evaluate its allergenic components; using IgE in the serum of patients with maple allergy.
Twenty-two patients with a clinical history of reaction and a positive skin-prick test to maple pollen extract were included in this study. Identification of IgE-binding proteins in A. velutinum pollen extract was performed by immunoblotting using sera from sensitive patients.
A protein band with a molecular weight of around 70 kDa was the most IgE-reactive allergen in A. velutinum pollen extract detected by this method.
Identification of a protein with a molecular weight of about 70kDa, as the most reactive allergen of A. velutinum pollen extract, can be considered as a potential allergen for designing diagnostic kits or as a target for immunotherapy of allergic patients with maple allergy.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3274</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3274/1796</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Altered Expression Levels of MicroRNA-155 and SOCS-1 in Peripheral Blood Mononuclear Cells of Newly Diagnosed Breast Cancer Patients</title>
    <FirstPage>12</FirstPage>
    <LastPage>19</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Sara</FirstName>
        <LastName>Iranparast</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran AND Student Research Committee, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Tahmasebi-Birgani</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran AND Cellular and Molecular Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Azim</FirstName>
        <LastName>Motamedfar</LastName>
        <affiliation locale="en_US">Department of Interventional Radiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran AND Department of Radiology, Golestan Hospital, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Afshin</FirstName>
        <LastName>Amari</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran AND Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehri</FirstName>
        <LastName>Ghafourian</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran AND Fertility, Infertility and Perinatology Research Center, Ahvaz Jundishapur University of Medical  Sciences, Ahvaz, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>04</Month>
        <Day>11</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>08</Month>
        <Day>04</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">MicroRNA-155 (miR-155) has a critical role in pro-inflammatory activation and tumor progression. In addition, miR-155 has various oncogenic effects in the tumor microenvironment by targeting the suppressor gene of cytokine signaling-1(SOCS-1) and interleukin-6 (IL-6). This study investigated the association of inflammatory changes with the variations of miR-155 expression in newly diagnosed breast cancer (NDBC) patients.
Seventy NDBC patients were categorized as lobular and ductal subgroups and forty healthy individuals participated in this study. The expression rate of miR-155 and its downstream target gene, SOCS-1, as well as the plasma levels of IL-6, were evaluated in peripheral blood mononuclear cells of NDBC patients; using real-time PCR and enzyme-linked immunosorbent assay, respectively.
Our results indicated an over-expression of miR-155 in the PBMCs of NDBC patients which was significantly associated with the tumor grade and the type of ductal carcinoma. In contrast, a significant downregulation of SOCS-1 was observed in NDBC patients compared to control group, however, there was no significant difference between two subtypes of BC. Furthermore, a higher concentration of plasma IL-6 was detected in NDBC patients compared to the healthy control group which had an inverse correlation with the SOCS-1 levels.
According to the potential effects of miR-155 on regulating the expression of SOCS-1 and IL-6, we suggest this small transcript as a promising diagnostic marker for various types of BC patients.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3185</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3185/1788</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Anaphylaxis in Cold Induced Urticaria: A Case Report  and Review of The Literature</title>
    <FirstPage>98</FirstPage>
    <LastPage>100</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Sandra</FirstName>
        <LastName>Gonz&#xE1;lez-D&#xED;az</LastName>
        <affiliation locale="en_US">Center of Allergy and Clinical Immunology, University Hospital Dr. Jos&#xE9; Eleuterio Gonz&#xE1;lez, Monterrey, Nuevo Le&#xF3;n, Mexico</affiliation>
      </Author>
      <Author>
        <FirstName>Elma</FirstName>
        <LastName>Fuentes-Lara</LastName>
        <affiliation locale="en_US">Center of Allergy and Clinical Immunology, University Hospital Dr. Jos&#xE9; Eleuterio Gonz&#xE1;lez, Monterrey, Nuevo Le&#xF3;n, Mexico</affiliation>
      </Author>
      <Author>
        <FirstName>Cindy</FirstName>
        <LastName>de Lira-Quezada</LastName>
        <affiliation locale="en_US">Center of Allergy and Clinical Immunology, University Hospital Dr. Jos&#xE9; Eleuterio Gonz&#xE1;lez, Monterrey, Nuevo Le&#xF3;n, Mexico</affiliation>
      </Author>
      <Author>
        <FirstName>Rosalaura</FirstName>
        <LastName>Villarreal-Gonz&#xE1;lez</LastName>
        <affiliation locale="en_US">Center of Allergy and Clinical Immunology, University Hospital Dr. Jos&#xE9; Eleuterio Gonz&#xE1;lez, Monterrey, Nuevo Le&#xF3;n, Mexico</affiliation>
      </Author>
      <Author>
        <FirstName>Rodrigo</FirstName>
        <LastName>de la Cruz-Cruz</LastName>
        <affiliation locale="en_US">Center of Allergy and Clinical Immunology, University Hospital Dr. Jos&#xE9; Eleuterio Gonz&#xE1;lez, Monterrey, Nuevo Le&#xF3;n, Mexico</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>03</Month>
        <Day>10</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>12</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Cold-induced urticaria is considered as a subtype of physical urticaria and also the second most common type of chronic inducible urticaria. Contact with cold surfaces or the environment may cause systemic reactions, especially during aquatic activities. A 22-year-old female patient with a history of sulfa drug allergy began her condition 2 years before the presence of generalized pruritic erythema with hives as well as 2 episodes that had been characterized by facial angioedema and syncope 3-5 minutes after being in contact with cold air or surfaces.&#xA0; On both events, she had just been outdoors on a cold, winter day. She was suspected to have cold-induced urticaria; thereby she had a positive reaction to the ice cube test. Due to the previous episodes of anaphylaxis, the patient was trained to administer intramuscular epinephrine. After 4 weeks of starting the treatment with antihistamines, no new events or injuries had occurred. Cold-induced urticaria may cause life-threatening reactions. The rate of anaphylaxis in these patients is low however, this case is presented to inform the importance of identifying this type of systemic reaction and preventing strategies.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3147</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3147/1799</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>21</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2022</Year>
        <Month>02</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Decreased Expression of Cytotoxic T Lymphocyte-associated Protein 4: A Risk Factor of Myocardial Infarction</title>
    <FirstPage>86</FirstPage>
    <LastPage>91</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Mansouri</LastName>
        <affiliation locale="en_US">Department of Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran AND Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mir Hosein</FirstName>
        <LastName>Seyed Mohammadzad</LastName>
        <affiliation locale="en_US">Department of Cardiology, Seyedoshohada Hospital, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>30</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Cardiovascular diseases are the most prevalent disease worldwide and pose a considerable threat to human health. Cytotoxic T lymphocyte-associated protein 4 (CTLA-4) plays a crucial role in the maintenance of immune diseases; however, its role in the progression of cardiovascular disorders is still unknow      <LastName>Fallahpour</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Hazrat Rasoul-E-Akram Hospital, Iran University of Medical Science, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sima</FirstName>
        <LastName>Shokri</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Hazrat Rasoul-E-Akram Hospital, Iran University of Medical Science, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Javad</FirstName>
        <LastName>Ahmadian</LastName>
        <affiliation locale="en_US">Department of Pediatric, Emam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Rasool</FirstName>
        <LastName>Molatefi</LastName>
        <affiliation locale="en_US">Department of Pediatrics, Bu Ali Hospital, Ardebil University of Medical Sciences, Ardebil, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Rekabi</LastName>
        <affiliation locale="en_US">Pediatric Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zeinab</FirstName>
        <LastName>Moinfar</LastName>
        <affiliation locale="en_US">Department of Community Medicine, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Paniz</FirstName>
        <LastName>Hashemitari</LastName>
        <affiliation locale="en_US">School of Medicine, Humanitas University, Milan, Italy</affiliation>
      </Author>
      <Author>
        <FirstName>Narges</FirstName>
        <LastName>Eslami</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Mofid Children&#x2019;s Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>08</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>02</Month>
        <Day>07</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Asthmatic patients may have aspirin-exacerbated respiratory disease and experience acute dyspnea and nasal symptoms within 3 hours after the ingestion of aspirin. This study aimed to evaluate the effect and outcome of daily low-dose aspirin in the treatment of moderate to severe asthma in patients with concomitant aspirin hypersensitivity and chronic rhinosinusitis with nasal polyposis (CRSwNP).
This clinical trial was conducted from February 2014 to February 2015 on 46 adult patients with moderate to severe asthma accompanied by CRSwNP. Patients with a positive aspirin challenge were blindly randomized in three groups receiving placebo/day (A); aspirin 100 mg/day (B); and aspirin 325mg/day (C), respectively. Clinical findings, FEV1 and ACT scores were recorded and compared before, during, and after treatment for 6 months.
Of 46 participants at baseline, 30 patients completed this 6-month trial study. The level of asthma control was significant; based on Asthma Control Test (ACT) when comparing the results in groups A and C and also groups B and C, but it was not significant when comparing ACT scores between groups A and B. FEV1 before and after treatment was significant when comparing groups A and B, groups A and C, and groups B and C.
To conclude, aspirin desensitization with a daily dose of 325 mg aspirin resulted in the improvement of long-term control of asthma. A daily aspirin dose of 100 mg was not associated with such an increase in ACT score.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2925</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/2925/1702</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Airborne Pollens and Their Association with Meteorological Parameters in the Atmosphere of Shiraz, Southwest Iran</title>
    <FirstPage>294</FirstPage>
    <LastPage>302</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Heidar Ali</FirstName>
        <LastName>Kafashan</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmad Reza</FirstName>
        <LastName>Khosravi</LastName>
        <affiliation locale="en_US">Department of Biology, Faculty of Science, Shiraz University, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Soheila</FirstName>
        <LastName>Alyasin</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Namazi Hospital, Shiraz, Iran AND Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Najmeh</FirstName>
        <LastName>Sepahi</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Kanannejad</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Farzaneh</FirstName>
        <LastName>Mohammad Ali Zadeh Shirazi</LastName>
        <affiliation locale="en_US">Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Sahar</FirstName>
        <LastName>Karami</LastName>
        <affiliation locale="en_US">Department of Biology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>03</Month>
        <Day>11</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Airborne pollen is considered one of the causative agents of hay fever, allergic rhinitis, conjunctivitis, and asthma. We aimed to investigate airborne pollens in the context of Shiraz located in the southwest of Iran and find their association with meteorological parameters.&#xA0;
The survey was conducted from October 2017 to September 2018, using seven days of volumetric Burkard spore trap, located in the center of the city.
A total of 5810 pollen grains/m3 belonging to 15 taxa were identified and recorded. Among them, 73.8% was the tree, while the grass, shrub, and weed constituted 13.56%, 3.5%, and 9.2% of total reported pollens, respectively. The major pollen types were Platanaceae (28.39%), Oleaceae (21.17%), Pinaceae (15.11%), Amaranthaceae (9.29%), and Brassicaceae (8.02%). A higher number of pollen counts and types were recorded in March, followed by September, while it was lower in May. Meteorological parameters were correlated with the monthly pollen counts. Wind speed was found to have a positive correlation with Platanaceae concentration. The significant correlation between pollen concentration and the temperature was positive for Poaceae, Amaranthaceae, and Plantaginaceae and negative for Rosaceae, Oleaceae, and Ulmaceae.&#xA0; Poaceae and Amaranthaceae were negatively correlated with humidity and positively with Rosaceae, Oleaceae, and Plantaginaceae. A negative correlation was found between rainfall and Poaceae and Amaranthaceae, while Plantaginaceae had a positive correlation with this parameter.
The results of this study may be helpful for allergologists in the diagnosis and treatment of airborne allergic disorders due to pollen grains.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3103</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3103/1706</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Investigation of rs531564 Polymorphism in the Primary MicroRNA-124 Gene in Patients with Systemic Lupus Erythematosus and Rheumatoid Arthritis: Association with Disease Susceptibility and Clinical Characteristics</title>
    <FirstPage>303</FirstPage>
    <LastPage>313</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>Hassani</LastName>
        <affiliation locale="en_US">School of Medicine, Aja University of Medical Science, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Dehani</LastName>
        <affiliation locale="en_US">School of Medicine, Aja University of Medical Science, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Zare Rafie</LastName>
        <affiliation locale="en_US">School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Emran</FirstName>
        <LastName>Esmaeilzadeh</LastName>
        <affiliation locale="en_US">Fetal Health Research Center, Hope Generation Foundation, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Saeideh</FirstName>
        <LastName>Davar</LastName>
        <affiliation locale="en_US">Department of Epidemiology and Biostatistics, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Bahram</FirstName>
        <LastName>Pakzad</LastName>
        <affiliation locale="en_US">Division of Rheumatology, Department of Internal Medicine, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Meysam</FirstName>
        <LastName>Mosallaei</LastName>
        <affiliation locale="en_US">School of Medicine, Aja University of Medical Science, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyyed Mohamad</FirstName>
        <LastName>Hoseini</LastName>
        <affiliation locale="en_US">Department of Pediatric, Semnan University of Medical Sciences, Semnan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hadi</FirstName>
        <LastName>Bayat</LastName>
        <affiliation locale="en_US">Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran AND Medical Nano-Technology and Tissue Engineering Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Soosanabadi</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, Semnan University of Medical Sciences, Semnan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>04</Month>
        <Day>12</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>05</Month>
        <Day>19</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">MicroRNA-124 (miR-124) is known as an important regulator of the immune system and inflammatory response. Studies have reported that this miRNA is dysregulated in autoimmune disorders such as systemic lupus erythematosus (SLE) and rheumatoid arthritis&#xA0;(RA). A functional analysis demonstrated that rs531564 (C&gt;G) affects the biogenesis of primary microRNA transcript-124 (pri-miR-124) and changes the expression of mature miR-124. In the present study, for the first time, we intended to evaluate the possible association between rs531564 polymorphism with SLE and RA risk.
&#xA0;In this case-control study, 110 patients with SLE, 115 patients with RA, and 120 healthy subjects were enrolled to evaluate rs531564 genotypes with real-time polymerase chain reaction (PCR) high resolution melting method.
Our findings demonstrated that frequency of GC genotype and G allele were considerably higher in the control group than RA patients, demonstrating that that GC genotype and G allele have a protective effect for healthy individuals (GC vs CC; OR: 0.29; 95%CI [0.12,0.67] and G vs C; OR: 0.42; 95%CI [0.23,0.78]). However, no significant correlation was confirmed between allele and genotype frequencies of rs531564 with SLE risk (p&gt;0.05). However, the G allele in rs531564 polymorphism was associated with serum level of C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), anti-dsDNA antibody, C3, C4, and creatinine, and frequency of renal involvements in SLE patients (p&lt;0.05). Moreover, in RA patients, the G was correlated with lower concentration ESR and CRP (p&lt;0.001).&#xA0;
Our findings propose a considerable association between rs531564 polymorphism in the pri-miR-124 gene with susceptibility and clinical characteristics of RA and SLE in the Iranian population.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3190</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3190/1719</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Inflammation in an Animal Model of Multiple Sclerosis Leads to MicroRNA-25-3p Dysregulation Associated with Inhibition of Pten and Klf4</title>
    <FirstPage>314</FirstPage>
    <LastPage>325</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Ameneh</FirstName>
        <LastName>Zare-Chahoki</LastName>
        <affiliation locale="en_US">Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences,  Kerman, Iran AND Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Meysam</FirstName>
        <LastName>Ahmadi-Zeidabadi</LastName>
        <affiliation locale="en_US">Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences,  Kerman, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Saeid</FirstName>
        <LastName>Azadarmaki</LastName>
        <affiliation locale="en_US">Clinical Laboratory, Khatam Alanbia Hospital, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Samira</FirstName>
        <LastName>Ghorbani</LastName>
        <affiliation locale="en_US">Hotchkiss Brain Institute and the Department of Clinical Neuroscience, University of Calgary, Calgary, Canada</affiliation>
      </Author>
      <Author>
        <FirstName>Farshid</FirstName>
        <LastName>Noorbakhsh</LastName>
        <affiliation locale="en_US">Shefa Neuroscience Research Center, Khatam Alanbia Hospital, Tehran, Iran  AND Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>02</Month>
        <Day>07</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>04</Month>
        <Day>27</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Perturbed expression of microRNAs (miRs) has been reported in different diseases including autoimmune and chronic inflammatory disorders. In this study, we investigated the expression of miR-25-3p and its targets in the central nervous system (CNS) tissue from mice with experimental autoimmune encephalomyelitis (EAE). We also analyzed the expression of miR-25 and its targets in activated macrophages and splenocytes.
EAE was induced in 12-week old female C57BL/6 mice; using myelin oligodendrocyte glycoprotein 35-55/complete Freund's adjuvant (MOG35-55/CFA) protocol. The expression of miR-25-3p and its targets, as well as the expression of inflammatory cytokines, were analyzed. We next established primary macrophage cultures as well as splenocyte cultures and evaluated the levels of miR-25-3p and its target genes in these cells following activation with lipopolysaccharide (LPS) and anti-CD3/anti-CD28 antibodies, respectively.
MiR-25-3p expression showed a strong positive correlation with the expression of tumor necrosis factor-alpha (TNF-&#x3B1;), interleukin (IL)-1&#x3B1;, and IL-6 pro-inflammatory cytokines. The expression of phosphatase and tensin homolog (Pten) and Kr&#xFC;ppel-like factor 4 (Klf4) was significantly reduced at the peak of the disease. Interestingly, Pten and Klf4 expression showed a significant negative correlation with miR-25-3p. Analysis of miR-25-3p expression in LPS-treated primary macrophages revealed significant upregulation in cells treated with 100ng/ml of LPS. This was associated with suppressed levels of miR-25-3p targets in these cells. However, anti-CD3/anti-CD28-stimulated splenocytes failed to show any alterations in miR-25-3p expression compared with vehicle-treated cells.
Our results indicate that miR-25-3p expression is likely induced by inflammatory mediators during autoimmune neuroinflammation. This upregulation is associated with decreased levels of Pten and Klf4, genes with known roles in cell cycle regulation and inflammation.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3120</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3120/1709</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Plasma Levels of MicroRNA-146a-5p, MicroRNA-24-3p, and MicroRNA-125a-5p as Potential Diagnostic Biomarkers for Rheumatoid Arthris</title>
    <FirstPage>326</FirstPage>
    <LastPage>337</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Safari</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Elia</FirstName>
        <LastName>Damavandi</LastName>
        <affiliation locale="en_US">Specialized Medical Genetic Center, Tehran Medical Sciences Branch of Academic Center for Education, Culture, and Research (ACECR), Tehran, Iran AND Department of Photo Healing and Regeneration, Yara Institute, Tehran Medical Sciences Branch of Academic Center for Education, Culture, and Research (ACECR), Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Abdol-Rahman</FirstName>
        <LastName>Rostamian</LastName>
        <affiliation locale="en_US">Department of Rheumatology, Imam Khomeini Hospital Complex, School of Medicine,  Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shafieh</FirstName>
        <LastName>Movassaghi</LastName>
        <affiliation locale="en_US">Department of Rheumatology, Imam Khomeini Hospital Complex, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zeinab</FirstName>
        <LastName>Imani-Saber</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mojtaba</FirstName>
        <LastName>Saffari</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>Kabuli</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Ghadami</LastName>
        <affiliation locale="en_US">Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran AND Endocrinology and Metabolism Research Institute, Tehran University of Medical Sciences, Tehran, Iran AND Cardiac Primary Prevention Research Center, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2020</Year>
        <Month>06</Month>
        <Day>10</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Rheumatoid arthritis (RA) is an autoimmune disease that is characterized by inflammation of the articular tissue. This study aims to evaluate the expression of microRNA (miR)-146a-5p, miR-24-3p, and miR-125a-5p in the plasma of RA patients and compare them with those of healthy controls to obtain a specific expression profile for earlier diagnosis and assistance in treating patients.
This study was performed on 50 RA patients and 50 healthy controls. Five microliters of blood were taken from each patient/control. Plasma RNA was extracted using the Trisol solution. cDNAs were synthesized; using moloney murine leukemia virus (MMLV) and deoxynucleoside triphosphate (dNTP). Real-time PCR was performed using SYBR green kit.
The mean expression of miR-146a-5p, miR-24-3p, and miR-125a-5p in the RA group were 8.1&#xB1;1.9, 6.5&#xB1;1.2, and 6.8&#xB1;2.2 and in the healthy group were 4.8&#xB1;1.6, 3.6&#xB1;2.2, and 3.4&#xB1;1.7, respectively. Significant differences were also observed in the mean expression of these three miRNAs in four subgroups of RA patients with different disease activity based on disease activity score 28 (DAS28) (p&lt;0.05). ROC curve analysis showed that miR-146a-5p (AUC=0.8, sensitivity= 96%, specificity=86%), miR-24-3p (AUC=0.7, Sensitivity=95%, Specificity=75%) and miR-125a-5p (AUC=0.71, sensitivity=93%, specificity=84%) could be used as suitable biomarkers for RA diagnosis.
Increased expressions of miR-146a-5p, miR-24-3p, and miR-125a-5p in RA patients indicate that the miRNAs are involved in disease incidence and progression, and the measurement of their expression can play an essential role in the diagnosis and treatment of the disease.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/2857</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/2857/1699</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Role of Fibroblast Activation Protein Alpha in Fibroblast-like Synoviocytes of Rheumatoid Arthritis</title>
    <FirstPage>338</FirstPage>
    <LastPage>349</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Mohammad Javad</FirstName>
        <LastName>Mousavi</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran AND Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran AND Department of Hematology, Faculty of Allied Medicine, Bushehr University of Medical Sciences, Bushehr, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Elham</FirstName>
        <LastName>Farhadi</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran AND Inflammation Research Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Vodjgani</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Jafar</FirstName>
        <LastName>Karami</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran AND Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran AND Department of Laboratory Sciences, Khomein University of Medical Sciences, Khomein, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Naghi</FirstName>
        <LastName>Tahmasebi</LastName>
        <affiliation locale="en_US">Division of Knee Surgery, Department of Orthopedics, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Arash</FirstName>
        <LastName>Sharafat Vaziri</LastName>
        <affiliation locale="en_US">Division of Knee Surgery, Department of Orthopedics, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Marzieh</FirstName>
        <LastName>Asgari</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nima</FirstName>
        <LastName>Rezaei</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran AND Research Center for Immunodeficiencies, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran AND Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Shayan</FirstName>
        <LastName>Mostafaei</LastName>
        <affiliation locale="en_US">Department of Biostatistics, Faculty of Health, Kermanshah University of Medical Sciences, Kermanshah, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmadreza</FirstName>
        <LastName>Jamshidi</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahdi</FirstName>
        <LastName>Mahmoudi</LastName>
        <affiliation locale="en_US">Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran AND Inflammation Research Center, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>02</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2021</Year>
        <Month>01</Month>
        <Day>20</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Fibroblast-like synoviocytes (FLSs) have been introduced in recent years as a key player in the pathogenesis of rheumatoid arthritis (RA), but the exact mechanisms of their transformation and intracellular pathways have not yet been determined. This study aimed to investigate the role of fibroblast activation protein-alpha (FAP-&#x3B1;) in the regulation of genes involved in the transformation and pathogenic activity of RA FLSs.
Synovial FLSs were isolated from RA patients and non-arthritic individuals (n=10 in both groups) and characterized; using immunocytochemistry and flow cytometry analysis. FLSs were divided into un-treated and Talabostat-treated groups to evaluate the FAP-&#x3B1; effect on the selected genes involved in cell cycle regulation (p21, p53, CCND1), apoptosis (Bcl-2, PUMA), and inflammatory and destructive behavior of FLSs (IL-6, TGF-&#x3B2;1, MMP-2, MMP-9, P2RX7). Gene expression analysis was performed by quantitative real-time polymerase chain reaction (qRT-PCR), and immunoblotting was carried out to evaluate FAP-&#x3B1; protein levels.
The basal level of FAP-&#x3B1; protein in RA patients was significantly higher than non-arthritic control individuals. However, no differences were observed between RA and non-arthritic FLSs,&#xA0;at the baseline mRNA levels of all the genes. Talabostat treatment significantly reduced FAP-&#x3B1; protein levels in both RA and non-arthritic FLSs, however, had no effect on mRNA expressions except an upregulated TGF-&#x3B2;1 expression in non-arthritic FLSs.
A significantly higher protein level of FAP-&#x3B1; in FLSs of RA patients compared with that of healthy individuals may point to the pathogenic role of this protein in RA FLSs. However, more investigations are necessary to address the mechanisms mediating the FAP-&#x3B1; pathogenic role in RA FLSs.&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/3084</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/3084/1695</pdf_url>
  </Article>
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Allergy, Asthma and Immunology</JournalTitle>
      <Issn>1735-1502</Issn>
      <Volume>20</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2021</Year>
        <Month>06</Month>
        <Day>06</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Genotyping of Human Platelet Antigen-1 to -5 and -15 by Polymerase Chain Reaction with Sequence-specific Primers (PCR-SSP) and Real-time PCR  in Az