<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Research in Molecular Medicine</title>
<title_fa>Research in Molecular Medicine</title_fa>
<short_title>Res Mol Med (RMM)</short_title>
<subject>Medical Sciences</subject>
<web_url>http://rmm.mazums.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2322-1348</journal_id_issn>
<journal_id_issn_online>2322-133X</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.29252/rmm</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1393</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2014</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>2</volume>
<number>3</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Association of FCγRIIA (CD32) polymorphism with susceptibility to brucellosis</title>
	<subject_fa>ايمونولوژي</subject_fa>
	<subject>Immunology</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Brucellosis is the major bacterial zoonoses of global importance caused by &lt;i&gt;Brucella spps.&lt;/i&gt; FC&amp;gamma;RIIA receptor plays a central role in phagocytosis of IgG2-opsonized bacteria. FC&amp;gamma;RIIA exhibits allelic polymorphisms with different capacities for binding IgG2 and phagocytosis. Cells expressing Fc &amp;gamma; RIIa-H131, bind more efficiently to complexes of IgG2 than those expressing the Fc &amp;gamma; RII A -R131 variant. The purpose of this study was to evaluate the association of FC&amp;gamma;RIIA polymorphisms with susceptibility to or severity of brucellosis.&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Materials and Methods: &lt;/strong&gt;In this study, we evaluated FC&amp;gamma;RIIA polymorphisms (R/R131, R/H131, H/H131) in 67 patients with brucellosis and 67 age, sex and geographical matched healthy volunteers. FC&amp;gamma;RIIA genotyping was performed by using a sequence-specific primer polymerase chain reaction (SSP-PCR).&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The comparison of the FC&amp;gamma;RIIA genotypes distribution in patients with brucellosis and controls showed a higher frequency in FC&amp;gamma;RIIA-R/R131 homozygosity in patients than controls (47.8% vs. 28.4%). Logistic regression analysis showed that there is a significant correlation between R/R131 genotype and brucellosis (OR=2.3, 95%CI=1.3-4.2, P=0.04). Although the frequency of the FC&amp;gamma;RIIA-R/R131 was higher in patients with chronic brucellosis compared with acute brucellosis, we did not find any statistically significant differences (53.8% vs. 46.3%, P=0.65).&lt;/p&gt;

&lt;p&gt;&lt;strong&gt;Conclusion: &lt;/strong&gt;The result of this study showed that the homozygous genotype of FC&amp;gamma;RIIA-R/R131 in patients with brucellosis may be associated with susceptibility to brucellosis as a genetic risk factor.&lt;/p&gt;

&lt;p&gt;&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Brucellosis,  FCγRIIA,  Polymorphism</keyword>
	<start_page>17</start_page>
	<end_page>22</end_page>
	<web_url>http://rmm.mazums.ac.ir/browse.php?a_code=A-10-25-3&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Zahra</first_name>
	<middle_name></middle_name>
	<last_name>Hosseini khah </last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846006089</code>
	<orcid>10031947532846006089</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>1Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Mazandaran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Zohreh</first_name>
	<middle_name></middle_name>
	<last_name>Bahadori</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846006090</code>
	<orcid>10031947532846006090</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>2Department of Microbiology, Faculty of Basic Sciences, Islamic Azad University, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Alireza</first_name>
	<middle_name></middle_name>
	<last_name>Rafiei</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>10031947532846006091</code>
	<orcid>10031947532846006091</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>1Molecular and Cell Biology Research Center, Mazandaran University of Medical Sciences, Mazandaran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mehrdad</first_name>
	<middle_name></middle_name>
	<last_name>Hajilooi</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rafiei1710@gmail.com</email>
	<code>10031947532846006092</code>
	<orcid>10031947532846006092</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>3Department of Immunology, Faculty of Medicine, Hamedan University of Medical Sciences, Hamedan, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
