<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Reports of Biochemistry and Molecular Biology</title>
<title_fa></title_fa>
<short_title>rbmb.net</short_title>
<subject>Basic Sciences</subject>
<web_url>http://rbmb.net</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2322-3480</journal_id_issn>
<journal_id_issn_online>2322-3480</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/rbmb</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>1401</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2022</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>11</volume>
<number>2</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>Development of Human Recombinant Antibodies Against ROR1 Tumor Antigen</title>
	<subject_fa>ایمنی شناسی</subject_fa>
	<subject>Immunology</subject>
	<content_type_fa>مقالات اصلی</content_type_fa>
	<content_type>Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Background: &lt;/em&gt;&lt;/strong&gt;Receptor tyrosine kinase-like orphan receptor 1 (ROR1) is an oncofetal antigen expressed on&amp;nbsp;many types of cancer cells, but not normal adult cells. ROR1 antigen contributes to cancer development and&amp;nbsp;progression by several signaling pathways. ROR1 expression has been associated with tumor growth,&amp;nbsp;survival, and metastasis. In this study specific human recombinant antibodies were selected against ROR1&amp;nbsp;antigen for their use in cancer immunotherapy.&lt;br&gt;
&lt;br&gt;
&lt;em&gt;&lt;strong&gt;Methods:&lt;/strong&gt;&lt;/em&gt; Phage display technology was used to produce phage antibody from a human scFv library. Phage&amp;nbsp;concentration was determined to confirm the phage rescue process. Panning procedure was performed to&amp;nbsp;isolate specific scFv clones against ROR1 epitope. Phage ELISA was done to evaluate the reactivity of the&amp;nbsp;selected scFvs.&lt;br&gt;
&lt;br&gt;
&lt;em&gt;&lt;strong&gt;Results:&lt;/strong&gt;&lt;/em&gt; Two specific human scFvs with frequencies of 20% and 25% were selected against ROR1 peptide.&amp;nbsp;The antibodies showed specific reaction to the corresponding epitopes in phage ELISA.&amp;nbsp;&lt;br&gt;
&lt;br&gt;
&lt;em&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;&lt;/em&gt;Cancer targeted therapy using human specific antibodies is a new strategy, which is used in&amp;nbsp;cancer therapy. The selected specific scFvs that target ROR1 epitope are human antibodies that originated&amp;nbsp;from a human library and have the potential to be used in clinic in cancer immunotherapy of ROR1 positive&amp;nbsp;tumors without induction of human anti mouse antibody (HAMA) response.&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>ROR1, Phage display, scFV library, Cancer.</keyword>
	<start_page>282</start_page>
	<end_page>288</end_page>
	<web_url>http://rbmb.net/browse.php?a_code=A-10-57-6&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Peyman </first_name>
	<middle_name></middle_name>
	<last_name>Bemani</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>100319475328460012217</code>
	<orcid>100319475328460012217</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Recombinant antibody laboratory, Department of Immunology, Shiraz University of Medical Sciences, Shiraz Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Setareh</first_name>
	<middle_name></middle_name>
	<last_name>Moazen</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>100319475328460012218</code>
	<orcid>100319475328460012218</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver BC, Canada.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Elham</first_name>
	<middle_name></middle_name>
	<last_name>Nadimi</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>100319475328460012219</code>
	<orcid>100319475328460012219</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Recombinant antibody laboratory, Department of Immunology, Shiraz University of Medical Sciences, Shiraz Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Foroogh </first_name>
	<middle_name></middle_name>
	<last_name>Nejatollahi</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>fnejatollaf@sums.ac.ir.</email>
	<code>100319475328460012220</code>
	<orcid>100319475328460012220</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Recombinant antibody laboratory, Department of Immunology, Shiraz University of Medical Sciences, Shiraz Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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