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mRNA vaccine development for cholangiocarcinoma: a precise pipeline
Cholangiocarcinoma (CHOL) is one of the most aggressive tumors worldwide and cannot be effectively treated by conventional and novel treatments, including immune checkpoint blockade therapy. The mRNA vaccine-based immunotherapeutic strategy has attracted much attention for various diseases, however,...
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Published in: | Military medical research 2022-07, Vol.9 (1), p.40-40, Article 40 |
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creator | Tang, Tian-Yu Huang, Xing Zhang, Gang Lu, Ming-Hao Liang, Ting-Bo |
description | Cholangiocarcinoma (CHOL) is one of the most aggressive tumors worldwide and cannot be effectively treated by conventional and novel treatments, including immune checkpoint blockade therapy. The mRNA vaccine-based immunotherapeutic strategy has attracted much attention for various diseases, however, its application in CHOL is limited due to the thoughtlessness in the integration of vaccine design and patient selection. A recent study established an integrated path for identifying potent CHOL antigens for mRNA vaccine development and a precise stratification for identifying CHOL patients who can benefit from the mRNA vaccines. In spite of a promising prospect, further investigations should identify immunogenic antigens and onco-immunological characteristics of CHOL to guide the clinical application of CHOL mRNA vaccines in the future. |
doi_str_mv | 10.1186/s40779-022-00399-8 |
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The mRNA vaccine-based immunotherapeutic strategy has attracted much attention for various diseases, however, its application in CHOL is limited due to the thoughtlessness in the integration of vaccine design and patient selection. A recent study established an integrated path for identifying potent CHOL antigens for mRNA vaccine development and a precise stratification for identifying CHOL patients who can benefit from the mRNA vaccines. In spite of a promising prospect, further investigations should identify immunogenic antigens and onco-immunological characteristics of CHOL to guide the clinical application of CHOL mRNA vaccines in the future.</description><identifier>ISSN: 2054-9369</identifier><identifier>ISSN: 2095-7467</identifier><identifier>EISSN: 2054-9369</identifier><identifier>DOI: 10.1186/s40779-022-00399-8</identifier><identifier>PMID: 35821067</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Antigens ; Bile Duct Neoplasms ; Bile Ducts, Intrahepatic ; Bioinformatics ; Cancer therapies ; Cholangiocarcinoma ; Cholangiocarcinoma (CHOL) ; Gene expression ; Genomes ; Genomics ; Growth factors ; Humans ; Immune microenvironment ; Immune subtype ; Immune system ; Immunotherapy ; Kinases ; Medical prognosis ; mRNA vaccine ; mRNA Vaccines ; Mutation ; Peptides ; Response rates ; RNA, Messenger ; Tumor antigen ; Tumors ; Vaccines, Synthetic</subject><ispartof>Military medical research, 2022-07, Vol.9 (1), p.40-40, Article 40</ispartof><rights>2022. The Author(s).</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-4e475dc0dccc3ee5830fcc5bf33701e9d29a0090996149baeab495adde6196a3</citedby><cites>FETCH-LOGICAL-c493t-4e475dc0dccc3ee5830fcc5bf33701e9d29a0090996149baeab495adde6196a3</cites><orcidid>0000-0002-8886-2777</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277828/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2691305361?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35821067$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tang, Tian-Yu</creatorcontrib><creatorcontrib>Huang, Xing</creatorcontrib><creatorcontrib>Zhang, Gang</creatorcontrib><creatorcontrib>Lu, Ming-Hao</creatorcontrib><creatorcontrib>Liang, Ting-Bo</creatorcontrib><title>mRNA vaccine development for cholangiocarcinoma: a precise pipeline</title><title>Military medical research</title><addtitle>Mil Med Res</addtitle><description>Cholangiocarcinoma (CHOL) is one of the most aggressive tumors worldwide and cannot be effectively treated by conventional and novel treatments, including immune checkpoint blockade therapy. The mRNA vaccine-based immunotherapeutic strategy has attracted much attention for various diseases, however, its application in CHOL is limited due to the thoughtlessness in the integration of vaccine design and patient selection. A recent study established an integrated path for identifying potent CHOL antigens for mRNA vaccine development and a precise stratification for identifying CHOL patients who can benefit from the mRNA vaccines. In spite of a promising prospect, further investigations should identify immunogenic antigens and onco-immunological characteristics of CHOL to guide the clinical application of CHOL mRNA vaccines in the future.</description><subject>Antigens</subject><subject>Bile Duct Neoplasms</subject><subject>Bile Ducts, Intrahepatic</subject><subject>Bioinformatics</subject><subject>Cancer therapies</subject><subject>Cholangiocarcinoma</subject><subject>Cholangiocarcinoma (CHOL)</subject><subject>Gene expression</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Growth factors</subject><subject>Humans</subject><subject>Immune microenvironment</subject><subject>Immune subtype</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>Kinases</subject><subject>Medical prognosis</subject><subject>mRNA vaccine</subject><subject>mRNA Vaccines</subject><subject>Mutation</subject><subject>Peptides</subject><subject>Response rates</subject><subject>RNA, Messenger</subject><subject>Tumor antigen</subject><subject>Tumors</subject><subject>Vaccines, Synthetic</subject><issn>2054-9369</issn><issn>2095-7467</issn><issn>2054-9369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkU1r3DAQhk1paUKaP9BDMfTSi9vRhyVND4Ww9CMQWii5C6003mixLVfaXci_r5JNQ9KThPTMw8y8TfOWwUfGjPpUJGiNHXDeAQjEzrxoTjn0skOh8OWT-0lzXsoWAJiQnCF_3ZyI3nAGSp82q-n3z4v24LyPM7WBDjSmZaJ51w4pt_4mjW7exORdrkCa3OfWtUsmHwu1S1xorGVvmleDGwudP5xnzfW3r9erH93Vr--Xq4urzksUu06S1H3wELz3gqg3Agbv-_UghAZGGDg6AARExSSuHbm1xN6FQIqhcuKsuTxqQ3Jbu-Q4uXxrk4v2_iHljXV5F_1IdgjcgDbYh8HJwUsnBqWNEqC8ZKBDdX05upb9eqLg68DZjc-kz3_meGM36WCRa224qYIPD4Kc_uyp7OwUi6exrovSvliuDIICwXhF3_-HbtM-z3VTlUImoBeKVYofKZ9TKZmGx2YY2LvE7TFxWxO394nbuy7ePR3jseRfvuIvIh-mhQ</recordid><startdate>20220712</startdate><enddate>20220712</enddate><creator>Tang, Tian-Yu</creator><creator>Huang, Xing</creator><creator>Zhang, Gang</creator><creator>Lu, Ming-Hao</creator><creator>Liang, Ting-Bo</creator><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88F</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M1Q</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8886-2777</orcidid></search><sort><creationdate>20220712</creationdate><title>mRNA vaccine development for cholangiocarcinoma: a precise pipeline</title><author>Tang, Tian-Yu ; Huang, Xing ; Zhang, Gang ; Lu, Ming-Hao ; Liang, Ting-Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-4e475dc0dccc3ee5830fcc5bf33701e9d29a0090996149baeab495adde6196a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antigens</topic><topic>Bile Duct Neoplasms</topic><topic>Bile Ducts, Intrahepatic</topic><topic>Bioinformatics</topic><topic>Cancer therapies</topic><topic>Cholangiocarcinoma</topic><topic>Cholangiocarcinoma (CHOL)</topic><topic>Gene expression</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Growth factors</topic><topic>Humans</topic><topic>Immune microenvironment</topic><topic>Immune subtype</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>Kinases</topic><topic>Medical prognosis</topic><topic>mRNA vaccine</topic><topic>mRNA Vaccines</topic><topic>Mutation</topic><topic>Peptides</topic><topic>Response rates</topic><topic>RNA, Messenger</topic><topic>Tumor antigen</topic><topic>Tumors</topic><topic>Vaccines, Synthetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tang, Tian-Yu</creatorcontrib><creatorcontrib>Huang, Xing</creatorcontrib><creatorcontrib>Zhang, Gang</creatorcontrib><creatorcontrib>Lu, Ming-Hao</creatorcontrib><creatorcontrib>Liang, Ting-Bo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Military Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Military Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Military medical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tang, Tian-Yu</au><au>Huang, Xing</au><au>Zhang, Gang</au><au>Lu, Ming-Hao</au><au>Liang, Ting-Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>mRNA vaccine development for cholangiocarcinoma: a precise pipeline</atitle><jtitle>Military medical research</jtitle><addtitle>Mil Med Res</addtitle><date>2022-07-12</date><risdate>2022</risdate><volume>9</volume><issue>1</issue><spage>40</spage><epage>40</epage><pages>40-40</pages><artnum>40</artnum><issn>2054-9369</issn><issn>2095-7467</issn><eissn>2054-9369</eissn><abstract>Cholangiocarcinoma (CHOL) is one of the most aggressive tumors worldwide and cannot be effectively treated by conventional and novel treatments, including immune checkpoint blockade therapy. The mRNA vaccine-based immunotherapeutic strategy has attracted much attention for various diseases, however, its application in CHOL is limited due to the thoughtlessness in the integration of vaccine design and patient selection. A recent study established an integrated path for identifying potent CHOL antigens for mRNA vaccine development and a precise stratification for identifying CHOL patients who can benefit from the mRNA vaccines. In spite of a promising prospect, further investigations should identify immunogenic antigens and onco-immunological characteristics of CHOL to guide the clinical application of CHOL mRNA vaccines in the future.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>35821067</pmid><doi>10.1186/s40779-022-00399-8</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-8886-2777</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens Bile Duct Neoplasms Bile Ducts, Intrahepatic Bioinformatics Cancer therapies Cholangiocarcinoma Cholangiocarcinoma (CHOL) Gene expression Genomes Genomics Growth factors Humans Immune microenvironment Immune subtype Immune system Immunotherapy Kinases Medical prognosis mRNA vaccine mRNA Vaccines Mutation Peptides Response rates RNA, Messenger Tumor antigen Tumors Vaccines, Synthetic |
title | mRNA vaccine development for cholangiocarcinoma: a precise pipeline |
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