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Vaccination of hormone-refractory prostate cancer patients with peptide cocktail-loaded dendritic cells: Results of a phase I clinical trial
Background Immunotherapies might represent promising alternatives for the treatment of patients with hormone‐refractory prostate cancer (HRPC). In a Phase I clinical trial, we evaluated a vaccination with dendritic cells (DCs) loaded with a cocktail consisting of HLA‐A*0201‐restricted peptides deriv...
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Published in: | The Prostate 2006-06, Vol.66 (8), p.811-821 |
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container_issue | 8 |
container_start_page | 811 |
container_title | The Prostate |
container_volume | 66 |
creator | Fuessel, Susanne Meye, Axel Schmitz, Marc Zastrow, Stefan Linné, Clemens Richter, Katja Löbel, Barbel Hakenberg, Oliver W. Hoelig, Kristina Rieber, E. Peter Wirth, Manfred P. |
description | Background
Immunotherapies might represent promising alternatives for the treatment of patients with hormone‐refractory prostate cancer (HRPC). In a Phase I clinical trial, we evaluated a vaccination with dendritic cells (DCs) loaded with a cocktail consisting of HLA‐A*0201‐restricted peptides derived from five different prostate cancer‐associated antigens [prostate‐specific antigen (PSA), prostate‐specific membrane antigen (PSMA), survivin, prostein, transient receptor potential p8 (trp‐p8)].
METHODS
Eight HRPC patients received a total of four vaccinations every other week. Clinical and immunological responses were monitored by the determination of the serum PSA levels and by enzyme linked immunospot (ELISPOT) analyses, respectively.
RESULTS
Apart from local skin reactions no side effects were noted. One patient displayed a partial response (PR; PSA decrease >50%) and three other patients showed stable PSA values or decelerated PSA increases. In ELISPOT analyses, three of four PSA responders also showed antigen‐specific CD8+ T‐cell activation against prostein, survivin, and PSMA.
CONCLUSIONS
The described protocol represents a safe and feasible concept for the induction of clinical and immunological responses. The application of a peptide cocktail‐derived from different antigens as a novel treatment modality is supposed to allow for the genetic and biologic heterogeneity of PCa. Prostate © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/pros.20404 |
format | article |
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Immunotherapies might represent promising alternatives for the treatment of patients with hormone‐refractory prostate cancer (HRPC). In a Phase I clinical trial, we evaluated a vaccination with dendritic cells (DCs) loaded with a cocktail consisting of HLA‐A*0201‐restricted peptides derived from five different prostate cancer‐associated antigens [prostate‐specific antigen (PSA), prostate‐specific membrane antigen (PSMA), survivin, prostein, transient receptor potential p8 (trp‐p8)].
METHODS
Eight HRPC patients received a total of four vaccinations every other week. Clinical and immunological responses were monitored by the determination of the serum PSA levels and by enzyme linked immunospot (ELISPOT) analyses, respectively.
RESULTS
Apart from local skin reactions no side effects were noted. One patient displayed a partial response (PR; PSA decrease >50%) and three other patients showed stable PSA values or decelerated PSA increases. In ELISPOT analyses, three of four PSA responders also showed antigen‐specific CD8+ T‐cell activation against prostein, survivin, and PSMA.
CONCLUSIONS
The described protocol represents a safe and feasible concept for the induction of clinical and immunological responses. The application of a peptide cocktail‐derived from different antigens as a novel treatment modality is supposed to allow for the genetic and biologic heterogeneity of PCa. Prostate © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0270-4137</identifier><identifier>EISSN: 1097-0045</identifier><identifier>DOI: 10.1002/pros.20404</identifier><identifier>PMID: 16482569</identifier><identifier>CODEN: PRSTDS</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Antigens, Surface - analysis ; Antigens, Surface - immunology ; Biological and medical sciences ; Cancer Vaccines - administration & dosage ; Cancer Vaccines - therapeutic use ; CD8-Positive T-Lymphocytes - immunology ; dendritic cells ; Dendritic Cells - immunology ; Drug Resistance, Neoplasm ; ELISPOT assay ; Glutamate Carboxypeptidase II - analysis ; Glutamate Carboxypeptidase II - immunology ; Gynecology. Andrology. Obstetrics ; HLA-A Antigens - chemistry ; HLA-A Antigens - immunology ; HLA-A Antigens - therapeutic use ; HLA-A2 Antigen ; hormone-refractory prostate cancer ; Humans ; Immunoenzyme Techniques ; Immunomagnetic Separation ; immunotherapy ; Immunotherapy, Active ; Inhibitor of Apoptosis Proteins ; Male ; Male genital diseases ; Medical sciences ; Membrane Proteins - analysis ; Membrane Proteins - immunology ; Microtubule-Associated Proteins - analysis ; Microtubule-Associated Proteins - immunology ; Middle Aged ; Neoplasm Proteins - analysis ; Neoplasm Proteins - immunology ; Nephrology. Urinary tract diseases ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - immunology ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - therapy ; T-cell response ; TRPM Cation Channels - analysis ; TRPM Cation Channels - immunology ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>The Prostate, 2006-06, Vol.66 (8), p.811-821</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3954-63100496ea6d193aa8858d4b5f765eeb0d7779ac89654f558caefbb453b4bd9a3</citedby><cites>FETCH-LOGICAL-c3954-63100496ea6d193aa8858d4b5f765eeb0d7779ac89654f558caefbb453b4bd9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17781876$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16482569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fuessel, Susanne</creatorcontrib><creatorcontrib>Meye, Axel</creatorcontrib><creatorcontrib>Schmitz, Marc</creatorcontrib><creatorcontrib>Zastrow, Stefan</creatorcontrib><creatorcontrib>Linné, Clemens</creatorcontrib><creatorcontrib>Richter, Katja</creatorcontrib><creatorcontrib>Löbel, Barbel</creatorcontrib><creatorcontrib>Hakenberg, Oliver W.</creatorcontrib><creatorcontrib>Hoelig, Kristina</creatorcontrib><creatorcontrib>Rieber, E. Peter</creatorcontrib><creatorcontrib>Wirth, Manfred P.</creatorcontrib><title>Vaccination of hormone-refractory prostate cancer patients with peptide cocktail-loaded dendritic cells: Results of a phase I clinical trial</title><title>The Prostate</title><addtitle>Prostate</addtitle><description>Background
Immunotherapies might represent promising alternatives for the treatment of patients with hormone‐refractory prostate cancer (HRPC). In a Phase I clinical trial, we evaluated a vaccination with dendritic cells (DCs) loaded with a cocktail consisting of HLA‐A*0201‐restricted peptides derived from five different prostate cancer‐associated antigens [prostate‐specific antigen (PSA), prostate‐specific membrane antigen (PSMA), survivin, prostein, transient receptor potential p8 (trp‐p8)].
METHODS
Eight HRPC patients received a total of four vaccinations every other week. Clinical and immunological responses were monitored by the determination of the serum PSA levels and by enzyme linked immunospot (ELISPOT) analyses, respectively.
RESULTS
Apart from local skin reactions no side effects were noted. One patient displayed a partial response (PR; PSA decrease >50%) and three other patients showed stable PSA values or decelerated PSA increases. In ELISPOT analyses, three of four PSA responders also showed antigen‐specific CD8+ T‐cell activation against prostein, survivin, and PSMA.
CONCLUSIONS
The described protocol represents a safe and feasible concept for the induction of clinical and immunological responses. The application of a peptide cocktail‐derived from different antigens as a novel treatment modality is supposed to allow for the genetic and biologic heterogeneity of PCa. Prostate © 2006 Wiley‐Liss, Inc.</description><subject>Aged</subject><subject>Antigens, Surface - analysis</subject><subject>Antigens, Surface - immunology</subject><subject>Biological and medical sciences</subject><subject>Cancer Vaccines - administration & dosage</subject><subject>Cancer Vaccines - therapeutic use</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>dendritic cells</subject><subject>Dendritic Cells - immunology</subject><subject>Drug Resistance, Neoplasm</subject><subject>ELISPOT assay</subject><subject>Glutamate Carboxypeptidase II - analysis</subject><subject>Glutamate Carboxypeptidase II - immunology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>HLA-A Antigens - chemistry</subject><subject>HLA-A Antigens - immunology</subject><subject>HLA-A Antigens - therapeutic use</subject><subject>HLA-A2 Antigen</subject><subject>hormone-refractory prostate cancer</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Immunomagnetic Separation</subject><subject>immunotherapy</subject><subject>Immunotherapy, Active</subject><subject>Inhibitor of Apoptosis Proteins</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Medical sciences</subject><subject>Membrane Proteins - analysis</subject><subject>Membrane Proteins - immunology</subject><subject>Microtubule-Associated Proteins - analysis</subject><subject>Microtubule-Associated Proteins - immunology</subject><subject>Middle Aged</subject><subject>Neoplasm Proteins - analysis</subject><subject>Neoplasm Proteins - immunology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - immunology</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - therapy</subject><subject>T-cell response</subject><subject>TRPM Cation Channels - analysis</subject><subject>TRPM Cation Channels - immunology</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><issn>0270-4137</issn><issn>1097-0045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kM1uEzEURi0EoqGw4QGQN7CoNMXO-GeGHapoKVQtBGiX1h37jmLqzAy2o5J34KFxSKA7Vl7c893r7xDynLNjztj89RTHdDxngokHZMZZqyvGhHxIZmyuWSV4rQ_Ik5S-M1ZwNn9MDrgSzVyqdkZ-XYO1foDsx4GOPV2OcTUOWEXsI9g8xg3drs-QkVoYLEY6FRiHnOidz0s64ZS9K8PR3mbwoQojOHTU4eCiz95SiyGkN3SBaR1KqhwBOi0hIT2nNvjBWwg0Rw_hKXnUQ0j4bP8ekm-n776evK8urs7OT95eVLZupahUXXqIViEox9saoGlk40Qne60kYsec1roF27RKil7KxgL2XSdk3YnOtVAfkle7vaXajzWmbFY-bb8JA47rZJRuuRCqKeDRDrTFQSpOzBT9CuLGcGa27s1WjvnjvsAv9lvX3QrdPbqXXYCXewBS6VwED9ane07rhjdaFY7vuDsfcPOfk-bT4urL3-PVLuNTxp__MhBvS5taS3NzeWauF-rDzedLZj7WvwG1MK5I</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>Fuessel, Susanne</creator><creator>Meye, Axel</creator><creator>Schmitz, Marc</creator><creator>Zastrow, Stefan</creator><creator>Linné, Clemens</creator><creator>Richter, Katja</creator><creator>Löbel, Barbel</creator><creator>Hakenberg, Oliver W.</creator><creator>Hoelig, Kristina</creator><creator>Rieber, E. Peter</creator><creator>Wirth, Manfred P.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20060601</creationdate><title>Vaccination of hormone-refractory prostate cancer patients with peptide cocktail-loaded dendritic cells: Results of a phase I clinical trial</title><author>Fuessel, Susanne ; Meye, Axel ; Schmitz, Marc ; Zastrow, Stefan ; Linné, Clemens ; Richter, Katja ; Löbel, Barbel ; Hakenberg, Oliver W. ; Hoelig, Kristina ; Rieber, E. Peter ; Wirth, Manfred P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3954-63100496ea6d193aa8858d4b5f765eeb0d7779ac89654f558caefbb453b4bd9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aged</topic><topic>Antigens, Surface - analysis</topic><topic>Antigens, Surface - immunology</topic><topic>Biological and medical sciences</topic><topic>Cancer Vaccines - administration & dosage</topic><topic>Cancer Vaccines - therapeutic use</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>dendritic cells</topic><topic>Dendritic Cells - immunology</topic><topic>Drug Resistance, Neoplasm</topic><topic>ELISPOT assay</topic><topic>Glutamate Carboxypeptidase II - analysis</topic><topic>Glutamate Carboxypeptidase II - immunology</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>HLA-A Antigens - chemistry</topic><topic>HLA-A Antigens - immunology</topic><topic>HLA-A Antigens - therapeutic use</topic><topic>HLA-A2 Antigen</topic><topic>hormone-refractory prostate cancer</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Immunomagnetic Separation</topic><topic>immunotherapy</topic><topic>Immunotherapy, Active</topic><topic>Inhibitor of Apoptosis Proteins</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Medical sciences</topic><topic>Membrane Proteins - analysis</topic><topic>Membrane Proteins - immunology</topic><topic>Microtubule-Associated Proteins - analysis</topic><topic>Microtubule-Associated Proteins - immunology</topic><topic>Middle Aged</topic><topic>Neoplasm Proteins - analysis</topic><topic>Neoplasm Proteins - immunology</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - immunology</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - therapy</topic><topic>T-cell response</topic><topic>TRPM Cation Channels - analysis</topic><topic>TRPM Cation Channels - immunology</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fuessel, Susanne</creatorcontrib><creatorcontrib>Meye, Axel</creatorcontrib><creatorcontrib>Schmitz, Marc</creatorcontrib><creatorcontrib>Zastrow, Stefan</creatorcontrib><creatorcontrib>Linné, Clemens</creatorcontrib><creatorcontrib>Richter, Katja</creatorcontrib><creatorcontrib>Löbel, Barbel</creatorcontrib><creatorcontrib>Hakenberg, Oliver W.</creatorcontrib><creatorcontrib>Hoelig, Kristina</creatorcontrib><creatorcontrib>Rieber, E. Peter</creatorcontrib><creatorcontrib>Wirth, Manfred P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Prostate</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fuessel, Susanne</au><au>Meye, Axel</au><au>Schmitz, Marc</au><au>Zastrow, Stefan</au><au>Linné, Clemens</au><au>Richter, Katja</au><au>Löbel, Barbel</au><au>Hakenberg, Oliver W.</au><au>Hoelig, Kristina</au><au>Rieber, E. Peter</au><au>Wirth, Manfred P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaccination of hormone-refractory prostate cancer patients with peptide cocktail-loaded dendritic cells: Results of a phase I clinical trial</atitle><jtitle>The Prostate</jtitle><addtitle>Prostate</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>66</volume><issue>8</issue><spage>811</spage><epage>821</epage><pages>811-821</pages><issn>0270-4137</issn><eissn>1097-0045</eissn><coden>PRSTDS</coden><abstract>Background
Immunotherapies might represent promising alternatives for the treatment of patients with hormone‐refractory prostate cancer (HRPC). In a Phase I clinical trial, we evaluated a vaccination with dendritic cells (DCs) loaded with a cocktail consisting of HLA‐A*0201‐restricted peptides derived from five different prostate cancer‐associated antigens [prostate‐specific antigen (PSA), prostate‐specific membrane antigen (PSMA), survivin, prostein, transient receptor potential p8 (trp‐p8)].
METHODS
Eight HRPC patients received a total of four vaccinations every other week. Clinical and immunological responses were monitored by the determination of the serum PSA levels and by enzyme linked immunospot (ELISPOT) analyses, respectively.
RESULTS
Apart from local skin reactions no side effects were noted. One patient displayed a partial response (PR; PSA decrease >50%) and three other patients showed stable PSA values or decelerated PSA increases. In ELISPOT analyses, three of four PSA responders also showed antigen‐specific CD8+ T‐cell activation against prostein, survivin, and PSMA.
CONCLUSIONS
The described protocol represents a safe and feasible concept for the induction of clinical and immunological responses. The application of a peptide cocktail‐derived from different antigens as a novel treatment modality is supposed to allow for the genetic and biologic heterogeneity of PCa. Prostate © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16482569</pmid><doi>10.1002/pros.20404</doi><tpages>11</tpages></addata></record> |
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subjects | Aged Antigens, Surface - analysis Antigens, Surface - immunology Biological and medical sciences Cancer Vaccines - administration & dosage Cancer Vaccines - therapeutic use CD8-Positive T-Lymphocytes - immunology dendritic cells Dendritic Cells - immunology Drug Resistance, Neoplasm ELISPOT assay Glutamate Carboxypeptidase II - analysis Glutamate Carboxypeptidase II - immunology Gynecology. Andrology. Obstetrics HLA-A Antigens - chemistry HLA-A Antigens - immunology HLA-A Antigens - therapeutic use HLA-A2 Antigen hormone-refractory prostate cancer Humans Immunoenzyme Techniques Immunomagnetic Separation immunotherapy Immunotherapy, Active Inhibitor of Apoptosis Proteins Male Male genital diseases Medical sciences Membrane Proteins - analysis Membrane Proteins - immunology Microtubule-Associated Proteins - analysis Microtubule-Associated Proteins - immunology Middle Aged Neoplasm Proteins - analysis Neoplasm Proteins - immunology Nephrology. Urinary tract diseases Prostate-Specific Antigen - blood Prostatic Neoplasms - immunology Prostatic Neoplasms - pathology Prostatic Neoplasms - therapy T-cell response TRPM Cation Channels - analysis TRPM Cation Channels - immunology Tumors Tumors of the urinary system Urinary tract. Prostate gland |
title | Vaccination of hormone-refractory prostate cancer patients with peptide cocktail-loaded dendritic cells: Results of a phase I clinical trial |
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