Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer
To date, extensive efforts to harness immunotherapeutic strategies for the treatment of pancreatic ductal adenocarcinoma (PDAC) have yielded disappointing results in clinical trials. These strategies mainly focused on cancer vaccines and immune checkpoint inhibitors alone or in combination with chem...
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Veröffentlicht in: | Cancers 2021-08, Vol.13 (16), p.4235 |
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description | To date, extensive efforts to harness immunotherapeutic strategies for the treatment of pancreatic ductal adenocarcinoma (PDAC) have yielded disappointing results in clinical trials. These strategies mainly focused on cancer vaccines and immune checkpoint inhibitors alone or in combination with chemotherapeutic or targeted agents. However, the growing preclinical and clinical data sets from these efforts have established valuable insights into the immunological characteristics of PDAC biology. Most notable are the immunosuppressive role of the tumour microenvironment (TME) and PDAC’s characteristically poor immunogenicity resulting from tumour intrinsic features. Moreover, PDAC tumour heterogeneity has been increasingly well characterized and may additionally limit a “one-fits-all” immunotherapeutic strategy. In this review, we first outline mechanisms of immunosuppression and immune evasion in PDAC. Secondly, we summarize recently published data on preclinical and clinical efforts to establish immunotherapeutic strategies for the treatment of PDAC including diverse combinatorial treatment approaches aiming at overcoming this resistance towards immunotherapeutic strategies. Particularly, these combinatorial treatment approaches seek to concomitantly increase PDAC antigenicity, boost PDAC directed T-cell responses, and impair the immunosuppressive character of the TME in order to allow immunotherapeutic agents to unleash their full potential. Eventually, the thorough understanding of the currently available data on immunotherapeutic treatment strategies of PDAC will enable researchers and clinicians to develop improved treatment regimens and to design innovative clinical trials to overcome the pronounced immunosuppression of PDAC. |
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These strategies mainly focused on cancer vaccines and immune checkpoint inhibitors alone or in combination with chemotherapeutic or targeted agents. However, the growing preclinical and clinical data sets from these efforts have established valuable insights into the immunological characteristics of PDAC biology. Most notable are the immunosuppressive role of the tumour microenvironment (TME) and PDAC’s characteristically poor immunogenicity resulting from tumour intrinsic features. Moreover, PDAC tumour heterogeneity has been increasingly well characterized and may additionally limit a “one-fits-all” immunotherapeutic strategy. In this review, we first outline mechanisms of immunosuppression and immune evasion in PDAC. Secondly, we summarize recently published data on preclinical and clinical efforts to establish immunotherapeutic strategies for the treatment of PDAC including diverse combinatorial treatment approaches aiming at overcoming this resistance towards immunotherapeutic strategies. Particularly, these combinatorial treatment approaches seek to concomitantly increase PDAC antigenicity, boost PDAC directed T-cell responses, and impair the immunosuppressive character of the TME in order to allow immunotherapeutic agents to unleash their full potential. Eventually, the thorough understanding of the currently available data on immunotherapeutic treatment strategies of PDAC will enable researchers and clinicians to develop improved treatment regimens and to design innovative clinical trials to overcome the pronounced immunosuppression of PDAC.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13164235</identifier><identifier>PMID: 34439389</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adenocarcinoma ; Antigenicity ; Antigens ; Apoptosis ; Cancer therapies ; Cancer vaccines ; Chemokines ; Chemotherapy ; Clinical trials ; Growth factors ; Immune checkpoint inhibitors ; Immune system ; Immunogenicity ; Immunosuppression ; Immunotherapy ; Lymphocytes T ; Medical prognosis ; Microenvironments ; Pancreatic cancer ; Patients ; Review ; Tumor microenvironment ; Tumors ; Vaccines</subject><ispartof>Cancers, 2021-08, Vol.13 (16), p.4235</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-9dc4230575d36510b7266c3b1491768fdb9a1d3c865596507b14a6f172bbde273</citedby><cites>FETCH-LOGICAL-c510t-9dc4230575d36510b7266c3b1491768fdb9a1d3c865596507b14a6f172bbde273</cites><orcidid>0000-0002-9349-2520</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/PMC8391691/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391691/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids></links><search><creatorcontrib>Wandmacher, Anna Maxi</creatorcontrib><creatorcontrib>Letsch, Anne</creatorcontrib><creatorcontrib>Sebens, Susanne</creatorcontrib><title>Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer</title><title>Cancers</title><description>To date, extensive efforts to harness immunotherapeutic strategies for the treatment of pancreatic ductal adenocarcinoma (PDAC) have yielded disappointing results in clinical trials. These strategies mainly focused on cancer vaccines and immune checkpoint inhibitors alone or in combination with chemotherapeutic or targeted agents. However, the growing preclinical and clinical data sets from these efforts have established valuable insights into the immunological characteristics of PDAC biology. Most notable are the immunosuppressive role of the tumour microenvironment (TME) and PDAC’s characteristically poor immunogenicity resulting from tumour intrinsic features. Moreover, PDAC tumour heterogeneity has been increasingly well characterized and may additionally limit a “one-fits-all” immunotherapeutic strategy. In this review, we first outline mechanisms of immunosuppression and immune evasion in PDAC. Secondly, we summarize recently published data on preclinical and clinical efforts to establish immunotherapeutic strategies for the treatment of PDAC including diverse combinatorial treatment approaches aiming at overcoming this resistance towards immunotherapeutic strategies. Particularly, these combinatorial treatment approaches seek to concomitantly increase PDAC antigenicity, boost PDAC directed T-cell responses, and impair the immunosuppressive character of the TME in order to allow immunotherapeutic agents to unleash their full potential. Eventually, the thorough understanding of the currently available data on immunotherapeutic treatment strategies of PDAC will enable researchers and clinicians to develop improved treatment regimens and to design innovative clinical trials to overcome the pronounced immunosuppression of PDAC.</description><subject>Adenocarcinoma</subject><subject>Antigenicity</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Cancer therapies</subject><subject>Cancer vaccines</subject><subject>Chemokines</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Growth factors</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune system</subject><subject>Immunogenicity</subject><subject>Immunosuppression</subject><subject>Immunotherapy</subject><subject>Lymphocytes T</subject><subject>Medical prognosis</subject><subject>Microenvironments</subject><subject>Pancreatic cancer</subject><subject>Patients</subject><subject>Review</subject><subject>Tumor microenvironment</subject><subject>Tumors</subject><subject>Vaccines</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkdFLwzAQxoMobsw9-1rwxZe5JNcmzYsgxbnBwD3oc0jTdOto05m0g_33Zm6I7l7uuPvx3XccQvcEPwEIPNXKauM8AcJiCskVGlLM6YQxEV__qQdo7P0WhwAgnPFbNIA4BgGpGKJ5tlF1beza-EjZIpr1Xe9MtAq6O6O7ah_6bRktmqa3bbcxTu0OUWWjVdjtjOoqHWU_Nu7QTalqb8bnPEKfs9ePbD5Zvr8tspflRCcEdxNR6OAVJzwpgIVOziljGnISi-AtLYtcKFKATlmSCJZgHiaKlYTTPC8M5TBCzyfdXZ83ptDGdk7VcueqRrmDbFUl_09stZHrdi9TEIQJEgQezwKu_eqN72RTeW3qWlnT9l7ShDEcx4xCQB8u0G3bOxvOO1Ix5xSICNT0RGnXeu9M-WuGYHl8lLx4FHwDtGKFWg</recordid><startdate>20210823</startdate><enddate>20210823</enddate><creator>Wandmacher, Anna Maxi</creator><creator>Letsch, Anne</creator><creator>Sebens, Susanne</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</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><orcidid>https://orcid.org/0000-0002-9349-2520</orcidid></search><sort><creationdate>20210823</creationdate><title>Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer</title><author>Wandmacher, Anna Maxi ; Letsch, Anne ; Sebens, Susanne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-9dc4230575d36510b7266c3b1491768fdb9a1d3c865596507b14a6f172bbde273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma</topic><topic>Antigenicity</topic><topic>Antigens</topic><topic>Apoptosis</topic><topic>Cancer therapies</topic><topic>Cancer vaccines</topic><topic>Chemokines</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Growth factors</topic><topic>Immune checkpoint inhibitors</topic><topic>Immune system</topic><topic>Immunogenicity</topic><topic>Immunosuppression</topic><topic>Immunotherapy</topic><topic>Lymphocytes T</topic><topic>Medical prognosis</topic><topic>Microenvironments</topic><topic>Pancreatic cancer</topic><topic>Patients</topic><topic>Review</topic><topic>Tumor microenvironment</topic><topic>Tumors</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wandmacher, Anna Maxi</creatorcontrib><creatorcontrib>Letsch, Anne</creatorcontrib><creatorcontrib>Sebens, Susanne</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wandmacher, Anna Maxi</au><au>Letsch, Anne</au><au>Sebens, Susanne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer</atitle><jtitle>Cancers</jtitle><date>2021-08-23</date><risdate>2021</risdate><volume>13</volume><issue>16</issue><spage>4235</spage><pages>4235-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>To date, extensive efforts to harness immunotherapeutic strategies for the treatment of pancreatic ductal adenocarcinoma (PDAC) have yielded disappointing results in clinical trials. These strategies mainly focused on cancer vaccines and immune checkpoint inhibitors alone or in combination with chemotherapeutic or targeted agents. However, the growing preclinical and clinical data sets from these efforts have established valuable insights into the immunological characteristics of PDAC biology. Most notable are the immunosuppressive role of the tumour microenvironment (TME) and PDAC’s characteristically poor immunogenicity resulting from tumour intrinsic features. Moreover, PDAC tumour heterogeneity has been increasingly well characterized and may additionally limit a “one-fits-all” immunotherapeutic strategy. In this review, we first outline mechanisms of immunosuppression and immune evasion in PDAC. Secondly, we summarize recently published data on preclinical and clinical efforts to establish immunotherapeutic strategies for the treatment of PDAC including diverse combinatorial treatment approaches aiming at overcoming this resistance towards immunotherapeutic strategies. Particularly, these combinatorial treatment approaches seek to concomitantly increase PDAC antigenicity, boost PDAC directed T-cell responses, and impair the immunosuppressive character of the TME in order to allow immunotherapeutic agents to unleash their full potential. 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subjects | Adenocarcinoma Antigenicity Antigens Apoptosis Cancer therapies Cancer vaccines Chemokines Chemotherapy Clinical trials Growth factors Immune checkpoint inhibitors Immune system Immunogenicity Immunosuppression Immunotherapy Lymphocytes T Medical prognosis Microenvironments Pancreatic cancer Patients Review Tumor microenvironment Tumors Vaccines |
title | Challenges and Future Perspectives of Immunotherapy in Pancreatic Cancer |
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