IMMU-03. UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS

Abstract BACKGROUND Glioblastoma (GBM) is the most aggressive form of primary brain cancer with no current cure. Immunotherapies, such as checkpoint blockade and adoptive T cell therapy, have effectively treated other cancers, but in GBM, these therapies have shown limited efficacy. This may be part...

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Veröffentlicht in:Neuro-oncology (Charlottesville, Va.) Va.), 2023-11, Vol.25 (Supplement_5), p.v141-v141
Hauptverfasser: Lee, Alexander, Sun, Lu, Chow, Frances, Treger, Janet, Cook, Danielle, Porter, Ely, Chen, Xi, Herrera, Gilbert, Everson, Richard, Liau, Linda, Cloughesy, Timothy, Hugo, Willy, Nathanson, David, Prins, Robert
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container_end_page v141
container_issue Supplement_5
container_start_page v141
container_title Neuro-oncology (Charlottesville, Va.)
container_volume 25
creator Lee, Alexander
Sun, Lu
Chow, Frances
Treger, Janet
Cook, Danielle
Porter, Ely
Chen, Xi
Herrera, Gilbert
Everson, Richard
Liau, Linda
Cloughesy, Timothy
Hugo, Willy
Nathanson, David
Prins, Robert
description Abstract BACKGROUND Glioblastoma (GBM) is the most aggressive form of primary brain cancer with no current cure. Immunotherapies, such as checkpoint blockade and adoptive T cell therapy, have effectively treated other cancers, but in GBM, these therapies have shown limited efficacy. This may be partially due to a lack of infiltrating tumor-reactive T cell populations capable of eliminating the tumor. METHODS & RESULTS We used single-cell RNA and TCRsequencing to examine the transcriptome and TCR repertoire of tumor-infiltrating T cells from a cohort of 32 recurrent GBM patients, 18 of whom had received neoadjuvant anti-PD-1 therapy. After dimensional reduction, we found that the cluster defined by T cell activation and exhaustion gene expression had the greatest number of expanded T cell clones and a transcriptomic profile similar to a previously published signature of tumor-reactive T cells. Focusing on a patient treated with neoadjuvant anti-PD-1 and a EGFRvIII Bispecific T cell engager therapy, we selected TCRs from T cells within the activated and exhausted cluster. Utilizing the PathFinder DNA Assembly technology developed by Rootpath, we generated a TCR library containing the selected TCRs and transduced the library into a fluorescent-reporter Jurkat line that measures T cell activation. We co-cultured the transduced Jurkats with the patient-derived gliomasphere, FACs sorted for activated Jurkats and performed TCR sequencing on the sorted cells. Six TCRs within the sorted population were over-represented relative to sorted T cells from control co-cultures, indicating their tumor reactivity. CONCLUSIONS In this study we provide a proof-of-concept framework for how incorporating silico single-cell analysis of a T cell’s transcriptome and TCR can be used to identity tumor-reactive T cells for potential downstream adoptive T cell therapies for patients with recurrent GBM.
doi_str_mv 10.1093/neuonc/noad179.0535
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UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>PubMed Central</source><creator>Lee, Alexander ; Sun, Lu ; Chow, Frances ; Treger, Janet ; Cook, Danielle ; Porter, Ely ; Chen, Xi ; Herrera, Gilbert ; Everson, Richard ; Liau, Linda ; Cloughesy, Timothy ; Hugo, Willy ; Nathanson, David ; Prins, Robert</creator><creatorcontrib>Lee, Alexander ; Sun, Lu ; Chow, Frances ; Treger, Janet ; Cook, Danielle ; Porter, Ely ; Chen, Xi ; Herrera, Gilbert ; Everson, Richard ; Liau, Linda ; Cloughesy, Timothy ; Hugo, Willy ; Nathanson, David ; Prins, Robert</creatorcontrib><description>Abstract BACKGROUND Glioblastoma (GBM) is the most aggressive form of primary brain cancer with no current cure. Immunotherapies, such as checkpoint blockade and adoptive T cell therapy, have effectively treated other cancers, but in GBM, these therapies have shown limited efficacy. This may be partially due to a lack of infiltrating tumor-reactive T cell populations capable of eliminating the tumor. METHODS &amp; RESULTS We used single-cell RNA and TCRsequencing to examine the transcriptome and TCR repertoire of tumor-infiltrating T cells from a cohort of 32 recurrent GBM patients, 18 of whom had received neoadjuvant anti-PD-1 therapy. After dimensional reduction, we found that the cluster defined by T cell activation and exhaustion gene expression had the greatest number of expanded T cell clones and a transcriptomic profile similar to a previously published signature of tumor-reactive T cells. Focusing on a patient treated with neoadjuvant anti-PD-1 and a EGFRvIII Bispecific T cell engager therapy, we selected TCRs from T cells within the activated and exhausted cluster. Utilizing the PathFinder DNA Assembly technology developed by Rootpath, we generated a TCR library containing the selected TCRs and transduced the library into a fluorescent-reporter Jurkat line that measures T cell activation. We co-cultured the transduced Jurkats with the patient-derived gliomasphere, FACs sorted for activated Jurkats and performed TCR sequencing on the sorted cells. Six TCRs within the sorted population were over-represented relative to sorted T cells from control co-cultures, indicating their tumor reactivity. CONCLUSIONS In this study we provide a proof-of-concept framework for how incorporating silico single-cell analysis of a T cell’s transcriptome and TCR can be used to identity tumor-reactive T cells for potential downstream adoptive T cell therapies for patients with recurrent GBM.</description><identifier>ISSN: 1522-8517</identifier><identifier>EISSN: 1523-5866</identifier><identifier>DOI: 10.1093/neuonc/noad179.0535</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Immunobiology</subject><ispartof>Neuro-oncology (Charlottesville, Va.), 2023-11, Vol.25 (Supplement_5), p.v141-v141</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639448/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639448/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids></links><search><creatorcontrib>Lee, Alexander</creatorcontrib><creatorcontrib>Sun, Lu</creatorcontrib><creatorcontrib>Chow, Frances</creatorcontrib><creatorcontrib>Treger, Janet</creatorcontrib><creatorcontrib>Cook, Danielle</creatorcontrib><creatorcontrib>Porter, Ely</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Herrera, Gilbert</creatorcontrib><creatorcontrib>Everson, Richard</creatorcontrib><creatorcontrib>Liau, Linda</creatorcontrib><creatorcontrib>Cloughesy, Timothy</creatorcontrib><creatorcontrib>Hugo, Willy</creatorcontrib><creatorcontrib>Nathanson, David</creatorcontrib><creatorcontrib>Prins, Robert</creatorcontrib><title>IMMU-03. UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS</title><title>Neuro-oncology (Charlottesville, Va.)</title><description>Abstract BACKGROUND Glioblastoma (GBM) is the most aggressive form of primary brain cancer with no current cure. Immunotherapies, such as checkpoint blockade and adoptive T cell therapy, have effectively treated other cancers, but in GBM, these therapies have shown limited efficacy. This may be partially due to a lack of infiltrating tumor-reactive T cell populations capable of eliminating the tumor. METHODS &amp; RESULTS We used single-cell RNA and TCRsequencing to examine the transcriptome and TCR repertoire of tumor-infiltrating T cells from a cohort of 32 recurrent GBM patients, 18 of whom had received neoadjuvant anti-PD-1 therapy. After dimensional reduction, we found that the cluster defined by T cell activation and exhaustion gene expression had the greatest number of expanded T cell clones and a transcriptomic profile similar to a previously published signature of tumor-reactive T cells. Focusing on a patient treated with neoadjuvant anti-PD-1 and a EGFRvIII Bispecific T cell engager therapy, we selected TCRs from T cells within the activated and exhausted cluster. Utilizing the PathFinder DNA Assembly technology developed by Rootpath, we generated a TCR library containing the selected TCRs and transduced the library into a fluorescent-reporter Jurkat line that measures T cell activation. We co-cultured the transduced Jurkats with the patient-derived gliomasphere, FACs sorted for activated Jurkats and performed TCR sequencing on the sorted cells. Six TCRs within the sorted population were over-represented relative to sorted T cells from control co-cultures, indicating their tumor reactivity. CONCLUSIONS In this study we provide a proof-of-concept framework for how incorporating silico single-cell analysis of a T cell’s transcriptome and TCR can be used to identity tumor-reactive T cells for potential downstream adoptive T cell therapies for patients with recurrent GBM.</description><subject>Immunobiology</subject><issn>1522-8517</issn><issn>1523-5866</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqNkU9unDAYxVHVSE2TnKAbX4CJDdhjVhV1zMSSB4-MidRuLAdMO1UCI-hU6rV6wniGKFJ3XX1_3-8tXhR9QnCFYJ7eDv44Du3tMLoOrfMVxCl-F10inKQxpoS8P_dJTDFaf4g-zvNPCBOECbqM_orttolhugKNEVJ8E9UGiArUoWcqlGojecy4lMDooqqZFjujtoKBoroDhmmw06oMz0FWKg3MPQfijldGlIIVRqjq_ChqJZdJlcA0W6VjzQtmxAM_Q5hUlTJfd7w-mWvOGq0DBGykUF9kUQfLAuwCISzr6-iid0-zv3mtV1FTcsPuY6k2wVTGLaIZjv1j73JCcgxJ7ynKOthB7HzuKaSwI3mW9LnrCU1y3-Ek67L1uqXOd562xJMkTa-izwv3cHx89l3rh1-Te7KHaf_spj92dHv772XY_7Dfx98WQZLmWUYDIV0I7TTO8-T7NzGC9hScXYKzr8HZU3BBtVpU4_HwX4IX5PqTcw</recordid><startdate>20231110</startdate><enddate>20231110</enddate><creator>Lee, Alexander</creator><creator>Sun, Lu</creator><creator>Chow, Frances</creator><creator>Treger, Janet</creator><creator>Cook, Danielle</creator><creator>Porter, Ely</creator><creator>Chen, Xi</creator><creator>Herrera, Gilbert</creator><creator>Everson, Richard</creator><creator>Liau, Linda</creator><creator>Cloughesy, Timothy</creator><creator>Hugo, Willy</creator><creator>Nathanson, David</creator><creator>Prins, Robert</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20231110</creationdate><title>IMMU-03. UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS</title><author>Lee, Alexander ; Sun, Lu ; Chow, Frances ; Treger, Janet ; Cook, Danielle ; Porter, Ely ; Chen, Xi ; Herrera, Gilbert ; Everson, Richard ; Liau, Linda ; Cloughesy, Timothy ; Hugo, Willy ; Nathanson, David ; Prins, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1845-ebfa9669506fe814d0d05ae9e8080d6942f9af6829ed524d477c8aede8c6e6233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Immunobiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Alexander</creatorcontrib><creatorcontrib>Sun, Lu</creatorcontrib><creatorcontrib>Chow, Frances</creatorcontrib><creatorcontrib>Treger, Janet</creatorcontrib><creatorcontrib>Cook, Danielle</creatorcontrib><creatorcontrib>Porter, Ely</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Herrera, Gilbert</creatorcontrib><creatorcontrib>Everson, Richard</creatorcontrib><creatorcontrib>Liau, Linda</creatorcontrib><creatorcontrib>Cloughesy, Timothy</creatorcontrib><creatorcontrib>Hugo, Willy</creatorcontrib><creatorcontrib>Nathanson, David</creatorcontrib><creatorcontrib>Prins, Robert</creatorcontrib><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Alexander</au><au>Sun, Lu</au><au>Chow, Frances</au><au>Treger, Janet</au><au>Cook, Danielle</au><au>Porter, Ely</au><au>Chen, Xi</au><au>Herrera, Gilbert</au><au>Everson, Richard</au><au>Liau, Linda</au><au>Cloughesy, Timothy</au><au>Hugo, Willy</au><au>Nathanson, David</au><au>Prins, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IMMU-03. UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS</atitle><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle><date>2023-11-10</date><risdate>2023</risdate><volume>25</volume><issue>Supplement_5</issue><spage>v141</spage><epage>v141</epage><pages>v141-v141</pages><issn>1522-8517</issn><eissn>1523-5866</eissn><abstract>Abstract BACKGROUND Glioblastoma (GBM) is the most aggressive form of primary brain cancer with no current cure. Immunotherapies, such as checkpoint blockade and adoptive T cell therapy, have effectively treated other cancers, but in GBM, these therapies have shown limited efficacy. This may be partially due to a lack of infiltrating tumor-reactive T cell populations capable of eliminating the tumor. METHODS &amp; RESULTS We used single-cell RNA and TCRsequencing to examine the transcriptome and TCR repertoire of tumor-infiltrating T cells from a cohort of 32 recurrent GBM patients, 18 of whom had received neoadjuvant anti-PD-1 therapy. After dimensional reduction, we found that the cluster defined by T cell activation and exhaustion gene expression had the greatest number of expanded T cell clones and a transcriptomic profile similar to a previously published signature of tumor-reactive T cells. Focusing on a patient treated with neoadjuvant anti-PD-1 and a EGFRvIII Bispecific T cell engager therapy, we selected TCRs from T cells within the activated and exhausted cluster. Utilizing the PathFinder DNA Assembly technology developed by Rootpath, we generated a TCR library containing the selected TCRs and transduced the library into a fluorescent-reporter Jurkat line that measures T cell activation. We co-cultured the transduced Jurkats with the patient-derived gliomasphere, FACs sorted for activated Jurkats and performed TCR sequencing on the sorted cells. Six TCRs within the sorted population were over-represented relative to sorted T cells from control co-cultures, indicating their tumor reactivity. CONCLUSIONS In this study we provide a proof-of-concept framework for how incorporating silico single-cell analysis of a T cell’s transcriptome and TCR can be used to identity tumor-reactive T cells for potential downstream adoptive T cell therapies for patients with recurrent GBM.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/neuonc/noad179.0535</doi><oa>free_for_read</oa></addata></record>
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); PubMed Central
subjects Immunobiology
title IMMU-03. UTILIZING IN SILICO SINGLE-CELL TRANSCRIPTOMIC AND TCR PROFILING FOR THE IDENTIFICATION AND ISOLATION OF TUMOR-REACTIVE TCR CLONOTYPES IN RECURRENT GLIOBLASTOMA PATIENTS
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