<?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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Bee Pollen Flavonoids as a Therapeutic Agent in Allergic  and Immunological Disorders</title>
    <FirstPage>171</FirstPage>
    <LastPage>182</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Masoomeh</FirstName>
        <LastName>Jannesar</LastName>
        <affiliation locale="en_US">Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran AND&#xA0;Department of Biology, Faculty of Sciences, Tehran University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Sharif Shoushtari</LastName>
        <affiliation locale="en_US">Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran AND&#xA0;Department of Biology, Faculty of Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmad</FirstName>
        <LastName>Majd</LastName>
        <affiliation locale="en_US">Department of Biology, Faculty of Sciences, North Tehran Branch, Islamic Azad University, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Pourpak</LastName>
        <affiliation locale="en_US">Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>10</Month>
        <Day>08</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>01</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Bee pollen grains, as the male reproductive part of seed-bearing plants contain considerable concentrations of various phytochemicals and nutrients. Since antiquity, people throughout the world used pollens to cure colds, flu, ulcers, premature aging, anemia and colitis. It is now well-documented that some bee pollen secondary metabolites (e.g. flavonoid) may have positive health effects. In recent years, the flavonoids have attracted much interest because of their wide range of biological properties and their beneficial effects on human health.&#xA0;The current review, points out potential therapeutic effects of bee pollen flavonoids as one of the main bee pollen bioactive compounds in allergic and immunological diseases. Due to the fact that some types of flavonoid components in bee pollen have anti-allergic, anti-oxidant and anti-inflammatory properties, bee pollen flavonoids can be excellent candidates for future studies including phytotherapy, molecular pharmacology and substitutes for chemicals used in treating allergic and immunological disorders.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1092</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1092/740</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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The Efficacy of Oral Immunotherapy in Patients with Cow's Milk Allergy</title>
    <FirstPage>183</FirstPage>
    <LastPage>192</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mohsen</FirstName>
        <LastName>Ebrahimi</LastName>
        <affiliation locale="en_US">Neonatal and Children's Health Research Center, Golestan University of Medical Sciences, Gorgan, Iran AND&#xA0;Department of Allergy and Clinical Immunology, Children&#x2019;s Medical Center,&#xA0;Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad</FirstName>
        <LastName>Gharagozlou</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Children&#x2019;s Medical Center,&#xA0;Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Mohebbi</LastName>
        <affiliation locale="en_US">Growth and Development Research Center, Children's&#xA0;Medical Center,&#xA0;Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Hafezi</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Gholamreza</FirstName>
        <LastName>Azizi</LastName>
        <affiliation locale="en_US">Non-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran; AND Department of Laboratory Medicine, Imam Hassan Mojtaba Hospital, Alborz University of Medical&#xA0;Sciences, Karaj, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoud</FirstName>
        <LastName>Movahedi</LastName>
        <affiliation locale="en_US">Department of Allergy and Clinical Immunology, Children&#x2019;s Medical Center,&#xA0;Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>04</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>09</Month>
        <Day>05</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Cow's milk allergy is the most common type of food allergy that decrease the quality of life of patients and their families. The aim of this study was to evaluate the efficacy of oral immunotherapy in patients with cow's milk allergy. 14 patients above 3 years of age with a history of cow's milk allergy confirmed by positive double blind placebo controlled food challenge (DBPCFC) test, presence of serum IgE against cow's milk and positive SPT (skin prick test) were enrolled in this study. During the immunotherapy all patients received increasing amounts of cow's milk during three phases. The type and severity of allergic reactions were recorded after each dose. The serum IgE and SPT were measured at the beginning and at the end of study.&#xA0;Since February 2014 to March 2015, 14 patients with the median age of 4.75 (3.7-7) years were studied. 13 patients (92.9%) completed the build up and maintenance phase successfully and became desensitized to cow's milk. During the build up and maintenance phase, 24 (2.0%) and 11 (0.9%) episodes of allergic reactions occurred, respectively.&#xA0;The median serum IgE level against cow's milk proteins and casein decreased from 39.3 to 10.4 and 7.72 to 2.83 (ku/L), respectively. The median of the difference of the wheal diameter in SPT with the control, decreased from 10 to 6 mm during the immunotherapy protocol.&#xA0;Oral immunotherapy is effective to decrease the frequency and the severity of allergic reactions but due to high rate of allergic reactions and possible anaphylaxis, it must be done under strict supervision of both clinicians and caregivers.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/898</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/898/741</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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Intradermal Skin Testing in Allergic Rhinitis and Asthma with Negative Skin Prick Tests</title>
    <FirstPage>193</FirstPage>
    <LastPage>197</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Fuat</FirstName>
        <LastName>Erel</LastName>
        <affiliation locale="en_US">Department of Pulmonary Medicine, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Nurhan</FirstName>
        <LastName>Sarioglu</LastName>
        <affiliation locale="en_US">Department of Pulmonary Medicine, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Mehmet</FirstName>
        <LastName>Kose</LastName>
        <affiliation locale="en_US">Department of Pulmonary Medicine, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Mustafa</FirstName>
        <LastName>Kaymakci</LastName>
        <affiliation locale="en_US">Department of Ear, Nose and Throat, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Mucahide</FirstName>
        <LastName>Gokcen</LastName>
        <affiliation locale="en_US">Department of Pulmonary Medicine, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Ahmet</FirstName>
        <LastName>Kepekci</LastName>
        <affiliation locale="en_US">Department of Ear, Nose and Throat, Meltem Hospital, Istanbul, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Mehmet</FirstName>
        <LastName>Arslan</LastName>
        <affiliation locale="en_US">Department of Health Public, Faculty of Medicine, Balikesir University, Balikesir, Turkey</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>04</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2016</Year>
        <Month>09</Month>
        <Day>13</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Taking medical history, physical examination, and performing some in vivo and in vitro tests are necessary for the diagnosis of allergy. Skin prick test (SPT) is considered as the standard method and first-line approach for the detection of allergic sensitization. Although mainly SPT is used for the detection of allergic sensitization, intradermal skin test (IDST) may be necessary, especially in patients with a negative SPT result. IDST is quite safe; however, is nowadays seldom used for detection of inhalant allergy and its value remains controversial. We aimed to investigate whether IDST is useful and necessary in diagnosis of respiratory allergies or not. This study involved 4223 patients with allergic rhinitis (AR) and/or bronchial asthma (BA). SPT results were positive in 2419 patients (57%) and negative in 1804 (43%). IDST was applied to 344 patients with marked allergic symptoms and with negative SPT results. Out of 344 patients, 152 (44%) showed allergic sensitization to IDST. The most commonly encountered allergic response was against the house dust mite (HDM) (32.6%). Allergic response against fungal spores was also relatively high (22%), while the pollen allergy rate (4.3%) was quite low. In BA patients with negative prick test, IDST made a significant contribution to the diagnosis of HDM allergy (p=0.003). To avoid missed diagnosis of AR and BA, particularly regarding &#xA0;the HDM allergy, application of IDST may be beneficial; therefore, IDST should be considered as the next step after SPT for diagnosis of allergy prior to in vitro or provocation tests.&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/889</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/889/734</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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The Effect of Salt Space on Clinical Findings and Peak Expiratory Flow in Children with Mild to Moderate Asthma: A Randomized Crossover Trial</title>
    <FirstPage>198</FirstPage>
    <LastPage>204</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Saeideh</FirstName>
        <LastName>Mazloomzadeh</LastName>
        <affiliation locale="en_US">Social Determinants of Health Research Center, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Niousha</FirstName>
        <LastName>Bakhshi</LastName>
        <affiliation locale="en_US">Mousavi Hospital, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Akefeh</FirstName>
        <LastName>Ahmadiafshar</LastName>
        <affiliation locale="en_US">Social Determinants of Health Research Center, Zanjan University of Medical Sciences, Zanjan, Iran AND&#xA0;Mousavi Hospital, Zanjan University of Medical Sciences, Zanjan, Iran AND&#xA0;Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehdi</FirstName>
        <LastName>Gholami</LastName>
        <affiliation locale="en_US">Zanjan Cultural Heritage Department, Zanjan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>01</Month>
        <Day>31</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The asthma treatment and control might be associated with significant burden on family and community&#x201A; thus exploring other therapeutic plans could be desirable. The aim of this study was to investigate the effect of salt space on clinical findings and peak expiratory flow rate among children with asthma. In this randomized crossover trial, 34 patients aged 6-14 years old with mild to moderate asthma were selected and randomly divided into two groups. The first group went through a period of salt therapy by staying in the salt room for one hour, three times a week for 3 consecutive weeks and then was under observation for three weeks. This process was reversed for the second group (three weeks under observation followed by salt therapy). The wash-out period was one week. During the study, the morning and evening peak expiratory flow (PEF), the frequency of coughing, wheezing, dyspnea and use of rescue medications were measured. Salt therapy had a significant effect on raising the morning and evening PEF in the second week in both groups (p=0.028 and p=0.032, respectively). However, there was no significant effect on PEF variabilities&#x201A; cough&#x201A; wheezing, dyspnea, and the frequency of rescue medication (p&gt;0.05). No side effect was observed during salt therapy. This study showed the significant effect of salt therapy on PEF rate of the patients in the second week. However, further studies with different frequency and time of salt therapy on respiratory disorders are recommended.&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1079</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1079/739</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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Effects of Intraperitoneal Injection of Allogeneic Bone Marrow-derived Mesenchymal Stem Cells on Bronchiolitis Obliterans in Mice Model</title>
    <FirstPage>205</FirstPage>
    <LastPage>218</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Sakine</FirstName>
        <LastName>I&#x15F;&#x131;k</LastName>
        <affiliation locale="en_US">Department of Pediatric Allergy and Immunology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Nevin</FirstName>
        <LastName>Uzuner</LastName>
        <affiliation locale="en_US">Department of Pediatric Allergy and Immunology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Meral</FirstName>
        <LastName>Karaman</LastName>
        <affiliation locale="en_US">Department of Microbiology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>&#xD6;zkan</FirstName>
        <LastName>Karaman</LastName>
        <affiliation locale="en_US">Department of Pediatric Allergy and Immunology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>M&#xFC;ge</FirstName>
        <LastName>K&#x131;ray</LastName>
        <affiliation locale="en_US">Department of Histology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>&#x130;lknur</FirstName>
        <LastName>Kozano&#x11F;lu</LastName>
        <affiliation locale="en_US">Department of Hematology, Ba&#x15F;kent University, Adana, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>H&#xFC;sn&#xFC;</FirstName>
        <LastName>Alper Ba&#x11F;r&#x131;yan&#x131;k</LastName>
        <affiliation locale="en_US">Department of Histology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Zeynep</FirstName>
        <LastName>Ar&#x131;kan-Ayy&#x131;ld&#x131;z</LastName>
        <affiliation locale="en_US">Department of Pediatric Allergy and Immunology, Dokuz Eylul University, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Melis</FirstName>
        <LastName>Kartal Yand&#x131;m</LastName>
        <affiliation locale="en_US">Department of Molecular Biology and Genetics, &#x130;zmir Institute of Technology, &#x130;zmir, Turkey</affiliation>
      </Author>
      <Author>
        <FirstName>Yusuf</FirstName>
        <LastName>Baran</LastName>
        <affiliation locale="en_US">Department of Molecular Biology and Genetics, &#x130;zmir Institute of Technology, &#x130;zmir, Turkey</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>07</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Bone marrow-derived mesenchymal stem cells (BMSCs) can ameliorate a variety of lung diseases such as asthma, lung fibrosis, and acute lung injury by its anti-inflammatory and immunmodulatory effects. In this study, we developed a mouse model of bronchiolitis obliterans (BO) and evaluated the effects of the intraperitoneal administration of BMSCs on lung histopathology and cytokine levels. 25 BALB/c mice were divided into four groups; control group (Group I), BO developed and 1x106&#xA0;BMSCs-injected group (Group II), non-BO, 1x106&#xA0;BMSCs-injected group (Group III), and BO developed and saline-injected group (Group IV). Histological and immunohistochemical findings of the lung tissue and the migration of BMSCs to the lung were evaluated using light and confocal microscopy techniques. Confocal microscopy evaluations showed that there was no noteworthy amount of BMSCs in the lung tissue of group III while significant amount of BMSCs was detected in group&#xA0;II. Wall thicknesses of terminal bronchiole and periterminal bronchiolar collagen deposition were significantly lower in group II compared to the group IV (p&lt;0.05). Furthermore, according to the immunohistochemical staining results, CD3, CD4, CD8, CD20, CD68 and neutrophil elastase positive immune cells of group II were stained more positive than group IV cells (p&lt;0.05). IFN-&#x3B3; IL-2 and TNF-&#x3B1; levels in bronchoalveolar lavage fluid (BALF) were significantly lower in group II compared to group IV (p&lt;0.05). The findings of this study indicate that intraperitoneally administered BMSCs have potent effects on histopatological changes of the lung tissue and cytokine levels in the murine model of BO.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1012</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1012/736</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>16</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="epublish">
        <Year>2017</Year>
        <Month>06</Month>
        <Day>17</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">The Effect of Oral Levamisole Co-administration on the Level of Immune Response to Hepatitis B Vaccine in Healthy Individuals:  A Randomized Clinical Trial</title>
    <FirstPage>219</FirstPage>
    <LastPage>227</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mousalreza</FirstName>
        <LastName>Hosseini</LastName>
        <affiliation locale="en_US">Department of Gasteroenterology and Hepatology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Payman</FirstName>
        <LastName>Shalchiantabrizi</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Maliheh</FirstName>
        <LastName>Dadgarmoghaddam</LastName>
        <affiliation locale="en_US">Department of Community Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Saeideh</FirstName>
        <LastName>Ahmady-Simab</LastName>
        <affiliation locale="en_US">The Vice Chancellor of Research, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Azizollah</FirstName>
        <LastName>Behjati</LastName>
        <affiliation locale="en_US">Immonology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Masoumeh</FirstName>
        <LastName>Salari</LastName>
        <affiliation locale="en_US">Department of Internal Medicine, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2016</Year>
        <Month>04</Month>
        <Day>09</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>02</Month>
        <Day>22liation locale="en_US">Otolaryngology Head and Neck Surgery Department, Beijing Children&#x2019;s Hospital,&#xA0;Capital Medical University, Beijing, China</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>02</Month>
        <Day>24</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>23</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">In the current study, we sought to track the clinical course of children under control-based asthma management and focused on respiratory pathogens monitoring. We prospectively explored influencing factors for asthma control. 121 children with uncontrolled asthma between 3-14 years of age were recruited. Common respiratory pathogens were detected with pharyngeal swabs and serum aeroallergen-specific IgE was measured. Numeric asthma control scores, airway resistance and fractional concentrations of exhaled nitric oxide (FENO) were evaluated. A proper control-based asthma management plan was established by the study physician. Regular reviews were performed, with the above measurements retested at set time intervals. The proportion of patients achieving asthma control at 1 month and 3 months were 59% and 76% ; respectively (p=0.013). These patients exhibited significant improvement in numeric scores and lung function parameters. The prevalence of common respiratory pathogens did not significantly differ between reviews. The number of sensitized aeroallergens significantly increased with age (r=0.235,&#xA0;p=0.010). Children with a high visual analogue scale (VAS) score for asthma at baseline were less likely to achieve asthma control after 1 month, while those sensitized to more aeroallergens were more likely to achieve asthma control after 1 month&#xA0;(p=0.016 and 0.012). In summary, children with asthma showed significant improvements in control rates and lung function during control-based asthma management, independent of respiratory pathogens testing reults. Patients with high VAS scores and fewer sensitizations to aeroallergens had difficulty achieving short-term asthma control.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1328</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1328/801</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>17</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Effects of Connexin 43 Inhibition in an Ovalbumin-induced Mouse Model of Asthma</title>
    <FirstPage>29</FirstPage>
    <LastPage>38</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Jian-Qiang</FirstName>
        <LastName>Huang</LastName>
        <affiliation locale="en_US">Department of Otolaryngology-Head and Neck Surgery, The Second Affiliated Hospital&#xA0;of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Xiao-Yang</FirstName>
        <LastName>Chen</LastName>
        <affiliation locale="en_US">Department of Respiratory Medicine, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Fang</FirstName>
        <LastName>Huang</LastName>
        <affiliation locale="en_US">Department of Otolaryngology-Head and Neck Surgery, The Second Affiliated Hospital&#xA0;of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Ji-Min</FirstName>
        <LastName>Fan</LastName>
        <affiliation locale="en_US">Department of Respiratory Medicine, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Xiao-Wei</FirstName>
        <LastName>Shi</LastName>
        <affiliation locale="en_US">Department of Otolaryngology-Head and Neck Surgery, The Second Affiliated Hospital&#xA0;of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Yan-Kai</FirstName>
        <LastName>Ju</LastName>
        <affiliation locale="en_US">Department of Otolaryngology-Head and Neck Surgery, The Second Affiliated Hospital&#xA0;of Fujian Medical University, Quanzhou, China</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>04</Month>
        <Day>03</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>04</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Connexion 43 (Cx43), a gap junction protein, is expressed abundantly in the airway and has been implicated in the pathogenesis of asthma. However, the effects of blocking Cx43 in asthma remain unclear. We investigated the therapeutic effects of two specific Cx43 inhibitors (Gap26 and Gap27) on the development of allergic airway disease in mice. Allergic asthma was induced in BALB/c mice by sensitization and challenge with ovalbumin (OVA). Different doses of Cx43 inhibitors were administered by aerosol inhalation 1 h after OVA challenge on days 21 and 23. Airway hyperresponsiveness (AHR), lung pathology, mucus production, and inflammatory cells and cytokines in bronchoalveolar lavage fluid (BALF) were examined. We found that Gap26 significantly inhibited OVA-induced AHR, inflammatory cell infiltration surrounding the bronchia, mucus production, inflammatory cells and cytokines in BALF, and OVA-specific IgE in the serum in a dose-dependent manner. Gap27 showed effects similar to those of Gap26 in inhibiting inflammatory cytokine production in BALF. We conclude Cx43 inhibitor inhalation alleviates asthma&#xA0;featuresin&#xA0;mice and may be a promising therapy for clinical asthma.

&#xA0;</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1387</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1387/804</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>17</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Regulatory Effect of Xiaoqinglong Decoction on Thymic Stromal Lymphopoietin (TSLP) Inflammation Promoter in Mice with Cold Asthma</title>
    <FirstPage>39</FirstPage>
    <LastPage>46</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Guihua</FirstName>
        <LastName>Song</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Yan</FirstName>
        <LastName>Zhang</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Kun</FirstName>
        <LastName>Zhao</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Mengmeng</FirstName>
        <LastName>Sun</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Pengju</FirstName>
        <LastName>Cheng</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
      <Author>
        <FirstName>Jing</FirstName>
        <LastName>Wang</LastName>
        <affiliation locale="en_US">Department of Pediatrics, The First Affiliated Hospital of Henan University of Traditional Chinese&#xA0;Medicine, Zhengzhou, China</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>04</Month>
        <Day>13</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Allergic asthma is a complex and chronic inflammatory airway disease. The thymic stromal lymphopoietin (TSLP) signaling pathway plays an important role in asthma. Xiaoqinglong Decoction (XQL) is the first choice to treat cold asthma in clinical settings. In this study, the role of the TSLP pathway in the onset of asthma and the protective mechanism of XQL were investigated. A total of 50 female mice were randomly divided into the following groups: the blank group (A), the model group (B), the XQL group (C), the dexamethasone group (D), and the XQL + dexamethasone group (E). Asthma was induced with ovalbumin, and corresponding drug intervention was carried out for 7 days, after which serum and lung tissue end points were analyzed.&#xA0;Serum interleukin 1&#x3B2; (IL-1&#x3B2;), tumor necrosis factor-&#x3B1; (TNF-&#x3B1;), nuclear factor &#x3BA;B (NF-&#x3BA;B), and TSLP levels were higher in group B than in group A (p&lt;0.05). However these levels were lower in group C and D than in group B (p&lt;0.05), and there was no significant difference between groups C and D (p&gt;0.05). Interestingly, these end points were significantly lower in group E than in groups C and D (p&lt;0.05). Regarding pathologic changes, the inflammatory infiltrate in the lungs of groups C, D, and E was lower than that of group B, especially in group E. We conclude that the TSLP pathway plays an important role in the course of asthma, and can be used as an important target for asthma treatment; XQL may play a role in reducing inflammation and relieving asthma by regulating the TSLP signaling pathway.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1410</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1410/812</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>17</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Myeloid-derived Suppressor Cells Elimination by 5-Fluorouracil Increased Dendritic Cell-based Vaccine Function and Improved Immunity in Tumor Mice</title>
    <FirstPage>47</FirstPage>
    <LastPage>55</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Najmeh</FirstName>
        <LastName>khosravianfar</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Jamshid</FirstName>
        <LastName>Hadjati</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Afshin</FirstName>
        <LastName>Namdar</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Roobina</FirstName>
        <LastName>Boghozian</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Morteza</FirstName>
        <LastName>Hafezi</LastName>
        <affiliation locale="en_US">Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahboubeh</FirstName>
        <LastName>Ashourpour</LastName>
        <affiliation locale="en_US">Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nasim</FirstName>
        <LastName>Kheshtchin</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahsa</FirstName>
        <LastName>Banitalebi</LastName>
        <affiliation locale="en_US">Department of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>Mirzaei</LastName>
        <affiliation locale="en_US">Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Seyed Alireza</FirstName>
        <LastName>Razavi</LastName>
        <affiliation locale="en_US">Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>09</Month>
        <Day>18</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Myeloid-derived suppressor cells (MDSCs) are capable of suppressing the immune response. 5-Fluorouracil (5-FU) compared to other chemotherapy drugs have shown considerable decreases in the number of MDSCs without visible effects on T, B and natural killer cells, as well as dendritic cells (DCs). DC-based vaccines considered to be appropriate candidates for cancer immunotherapy. However, due to the presence of various factors like MDSCs in tumor microenvironment, DC vaccine cannot effectively perform its function. The purpose of this study was to evaluate the effect of low doses of 5-FU on the efficacy of DC-based vaccines in preventing and treating of melanoma tumor model. This research was performed on 28 melanoma tumor bearing C57BL/6 female mice. The mice were randomly divided to 4 groups, group 1 is control population while group 2 and 3 were treated with DC vaccine and 5-FU respectively and group 4 was treated with both DC Vaccine and 5-FU. The mice survival, tumor growth rate, number of MDSC and CD8+/ CD107a+ T cells in mice spleen were evaluated in each group with maximum result in group 4. Our results revealed that combination of DC vaccine and 5-FU reduced number of MDSCs (3%) and also tumor growth rate(10%)(p&lt;0.05) and increased mice survival (70%) and increased CD8+ /CD107a+ T cells (25%). This study have shown that combinational therapy with DC vaccine improved immunity in tumor mice compared to the therapy consisting of DC vaccine or 5-FU only.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1331</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1331/813</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>17</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Indoleamine 2, 3-dioxygenase Up-regulates Hypoxia-inducible Factor-1&#x3B1; Expression by Degrading L-tryptophan but Not Its Activity in Human Alloreactive T-cells</title>
    <FirstPage>56</FirstPage>
    <LastPage>67</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Theodoros</FirstName>
        <LastName>Eleftheriadis</LastName>
        <affiliation locale="en_US">Department of Nephrology, Medical School, University of Thessaly, Larissa, Greece</affiliation>
      </Author>
      <Author>
        <FirstName>Georgios</FirstName>
        <LastName>Pissas</LastName>
        <affiliation locale="en_US">Department of Nephrology, Medical School, University of Thessaly, Larissa, Greece</affiliation>
      </Author>
      <Author>
        <FirstName>Vassilios</FirstName>
        <LastName>Liakopoulos</LastName>
        <affiliation locale="en_US">Department of Nephrology, Medical School, University of Thessaly, Larissa, Greece</affiliation>
      </Author>
      <Author>
        <FirstName>Ioannis</FirstName>
        <LastName>Stefanidis</LastName>
        <affiliation locale="en_US">Department of Nephrology, Medical School, University of Thessaly, Larissa, Greece</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>05</Month>
        <Day>06</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>07</Month>
        <Day>24</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Indoleamine 2, 3-dioxygenase (IDO) suppresses T-cell function at least in part by altering cell metabolism. Hypoxia-inducible factor-1 (HIF-1) increases upon T-cell activation and alters cell metabolism favoring their differentiation to effector cells. The effect of IDO on HIF-1&#x3B1; expression and activity was evaluated. For this purpose, mixed lymphocyte reaction (MLR) was performed using the IDO inhibitor 1-DL-methyl-tryptophan and the p53 inhibitor pifithrin-&#x3B1;. L-tryptophan degradation and cell proliferation were assessed by enzyme-linked immunosorbent assay, whereas the expression of proteins of interest by western blotting. IDO inhibited cell proliferation, and in MLR-derived T-cells increased HIF-1&#x3B1; and p53, whereas it decreased c-Myc. Inhibition of p53 abrogated IDO-induced HIF-1&#x3B1; upregulation. IDO increased the p53 transcriptional targets p21 and TP53-induced glycolysis and apoptosis regulator. The transcriptional targets of both HIF-1&#x3B1; and c-Myc, hexokinase II and lactate dehydrogenase-A were decreased by IDO. Phosphorylated pyruvate dehydrogenase remained unaffected indicating that pyruvate dehydrogenase kinase, a transcriptional target of HIF-1&#x3B1;, is not affected by IDO. In human alloreactive T-cells, IDO up-regulates HIF-1&#x3B1;, by inducing p53 overexpression. However, HIF-1&#x3B1; remains transcriptionally inactive.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1454</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1454/814</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>17</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>02</Month>
        <Day>26</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Th1-Th17 Ratio as a New Insight in Rheumatoid Arthritis Disease</title>
    <FirstPage>68</FirstPage>
    <LastPage>77</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Hadi</FirstName>
        <LastName>Bazzazi</LastName>
        <affiliation locale="en_US">Department of Molecular Medicine, School of Advanced Technologies in Medicine, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mehrdad</FirstName>
        <LastName>Aghaei</LastName>
        <affiliation locale="en_US">Golestan Rheumatology Research Center (GRRC), Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ali</FirstName>
        <LastName>Memarian</LastName>
        <affiliation locale="en_US">Stem Cell Research Center, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Hossein</FirstName>
        <LastName>Asgarian-Omran</LastName>
        <affiliation locale="en_US">Immunogenetics Research Center, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Nasser</FirstName>
        <LastName>Behnampour</LastName>
        <affiliation locale="en_US">Public Health Department, Faculty of Health, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Yaghoub</FirstName>
        <LastName>Yazdani</LastName>
        <affiliation locale="en_US">Infectious Diseases Research Center, Golestan University of Medical Sciences, Gorgan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>05</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>10</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">The Th17, Th1 and dual Th17/Th1 cells are important players in rheumatoid arthritis (RA) disease. To assess their roles, the frequency and impact of these cells were investigated in patients with different disease activity. In 14 new cases and 41 established RA patients in comparison with 22 healthy controls, the percentages of Th17, Th1 and dual Th17/Th1 cells were determined by flow-cytometry and their correlations were investigated with disease activity score (DAS28). Moreover, serum levels of IL-6 and IL-17 as inducer and functional cytokines for Th17 were investigated. Finally, serum levels of anti citrullinated protein antibody (ACPA) and rheumatoid factor (RF) were assessed. Percentage of Th17 cells in RA patients were increased in comparison with healthy controls (p&lt;0.01). In correlation with this finding, IL-17 and IL-6 cytokines in RA patients also increased (p&lt;0.01). The Th1 cells in RA patients were less than healthy group (p&lt;0.05) and showed negative correlation with disease activity (r=-0.328, p&lt;0.01). Dual Th17/Th1 cell only in new cases of RA were more than healthy control groups (p&lt;0.01). The Th1/Th17 ratio in RA patients is statistically different with healthy control group (p&lt;0.01) and it has negative correlation with disease activity (r=-264, p&lt;0.05). The levels of ACPA and RF were increased with disease progression. Decreasing of Th1/Th17 ratio in RA patient suggested a new paradigm in the field of autoimmune disease and indicated that imbalance or plasticity between these subsets can be important in progress, diagnosis and therapy of RA disease.</abstract>
    <web_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/view/1475</web_url>
    <pdf_url>https://ijaai.tums.ac.ir/index.php/ijaai/article/download/1475/805</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>
