Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients

The recurrence rates of Hepatocellular carcinoma (HCC) are high, necessitating novel and effective adjuvant therapies. Therefore, we conducted a phase II study of glypican-3 (GPC3) peptide vaccine as an adjuvant therapy for HCC patients. Forty-one patients with initial HCC who had undergone surgery...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Oncoimmunology 2016-05, Vol.5 (5), p.e1129483-e1129483
Hauptverfasser: Sawada, Yu, Yoshikawa, Toshiaki, Ofuji, Kazuya, Yoshimura, Mayuko, Tsuchiya, Nobuhiro, Takahashi, Mari, Nobuoka, Daisuke, Gotohda, Naoto, Takahashi, Shinichiro, Kato, Yuichiro, Konishi, Masaru, Kinoshita, Taira, Ikeda, Masafumi, Nakachi, Kohei, Yamazaki, Naoya, Mizuno, Shoichi, Takayama, Tadatoshi, Yamao, Kenji, Uesaka, Katsuhiko, Furuse, Junji, Endo, Itaru, Nakatsura, Tetsuya
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page e1129483
container_issue 5
container_start_page e1129483
container_title Oncoimmunology
container_volume 5
creator Sawada, Yu
Yoshikawa, Toshiaki
Ofuji, Kazuya
Yoshimura, Mayuko
Tsuchiya, Nobuhiro
Takahashi, Mari
Nobuoka, Daisuke
Gotohda, Naoto
Takahashi, Shinichiro
Kato, Yuichiro
Konishi, Masaru
Kinoshita, Taira
Ikeda, Masafumi
Nakachi, Kohei
Yamazaki, Naoya
Mizuno, Shoichi
Takayama, Tadatoshi
Yamao, Kenji
Uesaka, Katsuhiko
Furuse, Junji
Endo, Itaru
Nakatsura, Tetsuya
description The recurrence rates of Hepatocellular carcinoma (HCC) are high, necessitating novel and effective adjuvant therapies. Therefore, we conducted a phase II study of glypican-3 (GPC3) peptide vaccine as an adjuvant therapy for HCC patients. Forty-one patients with initial HCC who had undergone surgery or radiofrequency ablation (RFA) were analyzed in this phase II, open-label, single-arm trial. Ten vaccinations were performed for 1 y after curative treatment. We also investigated case-control subjects, where selected patients treated surgically during the same period were analyzed. The expression of GPC3 in the available primary tumors was determined by immunohistochemical analysis. Six patients received RFA therapy while 35 received surgery. The recurrence rate tended to be lower in the 35 patients treated with surgery plus vaccination compared to 33 patients who underwent surgery alone (28.6% vs. 54.3% and 39.4% vs. 54.5% at 1 and 2 y, respectively; p = 0.346, 0.983). Twenty-five patients treated with surgery and vaccination had GPC3-positive tumors; the recurrence rate in this group was significantly lower compared to that in 21 GPC3-positive patients who received surgery only (24% vs. 48% and 52.4% vs. 61.9% at 1 and 2 y, respectively; p = 0.047, 0.387). The GPC3 peptide vaccine improved the 1-y recurrence rate in patients with GPC3-positive tumors. This study demonstrated that GPC3 expression by the primary tumor may be used as a biomarker in a putative larger randomized clinical trial to determine the efficacy of the GPC3-derived peptide vaccine.
doi_str_mv 10.1080/2162402X.2015.1129483
format Article
fullrecord <record><control><sourceid>proquest_infor</sourceid><recordid>TN_cdi_proquest_miscellaneous_1807897039</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1807897039</sourcerecordid><originalsourceid>FETCH-LOGICAL-c520t-1b230d326208bb3c49657ab8ac2875460c3e3452ec19ec9c1ac03fa80c7b2dc63</originalsourceid><addsrcrecordid>eNp9UUuP0zAQthCIXS37E0A-cknxI07iCwJVsFRaiT2AxM2a2BPqVRIHOynqv8dRuxVc8MXWzPeY8UfIa842nDXsneCVKJn4sRGMqw3nQpeNfEau13qxNp5f3pxfkduUHlk-FVOV1C_JlajLqtaluibhYQ8J6W5H07y4Iw0dnfdI7x62snAY_QEdnXCavUN6AGv9iBQShZGCe1wOMM4rPsJ0pF2IdI8TzMFi3y89RGohZkYYgOayx3FOr8iLDvqEt-f7hnz__Onb9ktx__Vut_14X1gl2FzwVkjmpKgEa9pW2lJXqoa2ASuaWpUVsxJlqQRartFqy8Ey2UHDbN0KZyt5Q96fdKelHdDZ7B2hN1P0A8SjCeDNv53R783PcDCl5qxWIgu8PQvE8GvBNJvBp3UxGDEsyfCG1Y2umdQZqk5QG0NKEbuLDWdmzcs85WXWvMw5r8x78_eMF9ZTOhnw4QTwY_7cAX6H2Dszw7EPsYswWp-M_L_HHwwWpnU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1807897039</pqid></control><display><type>article</type><title>Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients</title><source>PubMed Central</source><creator>Sawada, Yu ; Yoshikawa, Toshiaki ; Ofuji, Kazuya ; Yoshimura, Mayuko ; Tsuchiya, Nobuhiro ; Takahashi, Mari ; Nobuoka, Daisuke ; Gotohda, Naoto ; Takahashi, Shinichiro ; Kato, Yuichiro ; Konishi, Masaru ; Kinoshita, Taira ; Ikeda, Masafumi ; Nakachi, Kohei ; Yamazaki, Naoya ; Mizuno, Shoichi ; Takayama, Tadatoshi ; Yamao, Kenji ; Uesaka, Katsuhiko ; Furuse, Junji ; Endo, Itaru ; Nakatsura, Tetsuya</creator><creatorcontrib>Sawada, Yu ; Yoshikawa, Toshiaki ; Ofuji, Kazuya ; Yoshimura, Mayuko ; Tsuchiya, Nobuhiro ; Takahashi, Mari ; Nobuoka, Daisuke ; Gotohda, Naoto ; Takahashi, Shinichiro ; Kato, Yuichiro ; Konishi, Masaru ; Kinoshita, Taira ; Ikeda, Masafumi ; Nakachi, Kohei ; Yamazaki, Naoya ; Mizuno, Shoichi ; Takayama, Tadatoshi ; Yamao, Kenji ; Uesaka, Katsuhiko ; Furuse, Junji ; Endo, Itaru ; Nakatsura, Tetsuya</creatorcontrib><description>The recurrence rates of Hepatocellular carcinoma (HCC) are high, necessitating novel and effective adjuvant therapies. Therefore, we conducted a phase II study of glypican-3 (GPC3) peptide vaccine as an adjuvant therapy for HCC patients. Forty-one patients with initial HCC who had undergone surgery or radiofrequency ablation (RFA) were analyzed in this phase II, open-label, single-arm trial. Ten vaccinations were performed for 1 y after curative treatment. We also investigated case-control subjects, where selected patients treated surgically during the same period were analyzed. The expression of GPC3 in the available primary tumors was determined by immunohistochemical analysis. Six patients received RFA therapy while 35 received surgery. The recurrence rate tended to be lower in the 35 patients treated with surgery plus vaccination compared to 33 patients who underwent surgery alone (28.6% vs. 54.3% and 39.4% vs. 54.5% at 1 and 2 y, respectively; p = 0.346, 0.983). Twenty-five patients treated with surgery and vaccination had GPC3-positive tumors; the recurrence rate in this group was significantly lower compared to that in 21 GPC3-positive patients who received surgery only (24% vs. 48% and 52.4% vs. 61.9% at 1 and 2 y, respectively; p = 0.047, 0.387). The GPC3 peptide vaccine improved the 1-y recurrence rate in patients with GPC3-positive tumors. This study demonstrated that GPC3 expression by the primary tumor may be used as a biomarker in a putative larger randomized clinical trial to determine the efficacy of the GPC3-derived peptide vaccine.</description><identifier>ISSN: 2162-4011</identifier><identifier>ISSN: 2162-402X</identifier><identifier>EISSN: 2162-402X</identifier><identifier>DOI: 10.1080/2162402X.2015.1129483</identifier><identifier>PMID: 27467945</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Adjuvant therapy ; CTL ; glypican-3 ; HCC ; Original Research ; peptide vaccine</subject><ispartof>Oncoimmunology, 2016-05, Vol.5 (5), p.e1129483-e1129483</ispartof><rights>2016 The Author(s). Published with license by Taylor &amp; Francis Group, LLC © Yu Sawada, Toshiaki Yoshikawa, Kazuya Ofuji, Mayuko Yoshimura, Nobuhiro Tsuchiya, Mari Takahashi, Daisuke Nobuoka, Naoto Gotohda, Shinichiro Takahashi, Yuichiro Kato, Masaru Konishi, Taira Kinoshita, Masafumi Ikeda, Kohei Nakachi, Naoya Yamazaki, Shoichi Mizuno, Tadatoshi Takayama, Kenji Yamao, Katsuhiko Uesaka, Junji Furuse, Itaru Endo, and Tetsuya Nakatsura. 2016</rights><rights>2016 The Author(s). Published with license by Taylor &amp; Francis Group, LLC 2016 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-1b230d326208bb3c49657ab8ac2875460c3e3452ec19ec9c1ac03fa80c7b2dc63</citedby><cites>FETCH-LOGICAL-c520t-1b230d326208bb3c49657ab8ac2875460c3e3452ec19ec9c1ac03fa80c7b2dc63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910752/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910752/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27467945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sawada, Yu</creatorcontrib><creatorcontrib>Yoshikawa, Toshiaki</creatorcontrib><creatorcontrib>Ofuji, Kazuya</creatorcontrib><creatorcontrib>Yoshimura, Mayuko</creatorcontrib><creatorcontrib>Tsuchiya, Nobuhiro</creatorcontrib><creatorcontrib>Takahashi, Mari</creatorcontrib><creatorcontrib>Nobuoka, Daisuke</creatorcontrib><creatorcontrib>Gotohda, Naoto</creatorcontrib><creatorcontrib>Takahashi, Shinichiro</creatorcontrib><creatorcontrib>Kato, Yuichiro</creatorcontrib><creatorcontrib>Konishi, Masaru</creatorcontrib><creatorcontrib>Kinoshita, Taira</creatorcontrib><creatorcontrib>Ikeda, Masafumi</creatorcontrib><creatorcontrib>Nakachi, Kohei</creatorcontrib><creatorcontrib>Yamazaki, Naoya</creatorcontrib><creatorcontrib>Mizuno, Shoichi</creatorcontrib><creatorcontrib>Takayama, Tadatoshi</creatorcontrib><creatorcontrib>Yamao, Kenji</creatorcontrib><creatorcontrib>Uesaka, Katsuhiko</creatorcontrib><creatorcontrib>Furuse, Junji</creatorcontrib><creatorcontrib>Endo, Itaru</creatorcontrib><creatorcontrib>Nakatsura, Tetsuya</creatorcontrib><title>Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients</title><title>Oncoimmunology</title><addtitle>Oncoimmunology</addtitle><description>The recurrence rates of Hepatocellular carcinoma (HCC) are high, necessitating novel and effective adjuvant therapies. Therefore, we conducted a phase II study of glypican-3 (GPC3) peptide vaccine as an adjuvant therapy for HCC patients. Forty-one patients with initial HCC who had undergone surgery or radiofrequency ablation (RFA) were analyzed in this phase II, open-label, single-arm trial. Ten vaccinations were performed for 1 y after curative treatment. We also investigated case-control subjects, where selected patients treated surgically during the same period were analyzed. The expression of GPC3 in the available primary tumors was determined by immunohistochemical analysis. Six patients received RFA therapy while 35 received surgery. The recurrence rate tended to be lower in the 35 patients treated with surgery plus vaccination compared to 33 patients who underwent surgery alone (28.6% vs. 54.3% and 39.4% vs. 54.5% at 1 and 2 y, respectively; p = 0.346, 0.983). Twenty-five patients treated with surgery and vaccination had GPC3-positive tumors; the recurrence rate in this group was significantly lower compared to that in 21 GPC3-positive patients who received surgery only (24% vs. 48% and 52.4% vs. 61.9% at 1 and 2 y, respectively; p = 0.047, 0.387). The GPC3 peptide vaccine improved the 1-y recurrence rate in patients with GPC3-positive tumors. This study demonstrated that GPC3 expression by the primary tumor may be used as a biomarker in a putative larger randomized clinical trial to determine the efficacy of the GPC3-derived peptide vaccine.</description><subject>Adjuvant therapy</subject><subject>CTL</subject><subject>glypican-3</subject><subject>HCC</subject><subject>Original Research</subject><subject>peptide vaccine</subject><issn>2162-4011</issn><issn>2162-402X</issn><issn>2162-402X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><recordid>eNp9UUuP0zAQthCIXS37E0A-cknxI07iCwJVsFRaiT2AxM2a2BPqVRIHOynqv8dRuxVc8MXWzPeY8UfIa842nDXsneCVKJn4sRGMqw3nQpeNfEau13qxNp5f3pxfkduUHlk-FVOV1C_JlajLqtaluibhYQ8J6W5H07y4Iw0dnfdI7x62snAY_QEdnXCavUN6AGv9iBQShZGCe1wOMM4rPsJ0pF2IdI8TzMFi3y89RGohZkYYgOayx3FOr8iLDvqEt-f7hnz__Onb9ktx__Vut_14X1gl2FzwVkjmpKgEa9pW2lJXqoa2ASuaWpUVsxJlqQRartFqy8Ey2UHDbN0KZyt5Q96fdKelHdDZ7B2hN1P0A8SjCeDNv53R783PcDCl5qxWIgu8PQvE8GvBNJvBp3UxGDEsyfCG1Y2umdQZqk5QG0NKEbuLDWdmzcs85WXWvMw5r8x78_eMF9ZTOhnw4QTwY_7cAX6H2Dszw7EPsYswWp-M_L_HHwwWpnU</recordid><startdate>20160503</startdate><enddate>20160503</enddate><creator>Sawada, Yu</creator><creator>Yoshikawa, Toshiaki</creator><creator>Ofuji, Kazuya</creator><creator>Yoshimura, Mayuko</creator><creator>Tsuchiya, Nobuhiro</creator><creator>Takahashi, Mari</creator><creator>Nobuoka, Daisuke</creator><creator>Gotohda, Naoto</creator><creator>Takahashi, Shinichiro</creator><creator>Kato, Yuichiro</creator><creator>Konishi, Masaru</creator><creator>Kinoshita, Taira</creator><creator>Ikeda, Masafumi</creator><creator>Nakachi, Kohei</creator><creator>Yamazaki, Naoya</creator><creator>Mizuno, Shoichi</creator><creator>Takayama, Tadatoshi</creator><creator>Yamao, Kenji</creator><creator>Uesaka, Katsuhiko</creator><creator>Furuse, Junji</creator><creator>Endo, Itaru</creator><creator>Nakatsura, Tetsuya</creator><general>Taylor &amp; Francis</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160503</creationdate><title>Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients</title><author>Sawada, Yu ; Yoshikawa, Toshiaki ; Ofuji, Kazuya ; Yoshimura, Mayuko ; Tsuchiya, Nobuhiro ; Takahashi, Mari ; Nobuoka, Daisuke ; Gotohda, Naoto ; Takahashi, Shinichiro ; Kato, Yuichiro ; Konishi, Masaru ; Kinoshita, Taira ; Ikeda, Masafumi ; Nakachi, Kohei ; Yamazaki, Naoya ; Mizuno, Shoichi ; Takayama, Tadatoshi ; Yamao, Kenji ; Uesaka, Katsuhiko ; Furuse, Junji ; Endo, Itaru ; Nakatsura, Tetsuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-1b230d326208bb3c49657ab8ac2875460c3e3452ec19ec9c1ac03fa80c7b2dc63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adjuvant therapy</topic><topic>CTL</topic><topic>glypican-3</topic><topic>HCC</topic><topic>Original Research</topic><topic>peptide vaccine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sawada, Yu</creatorcontrib><creatorcontrib>Yoshikawa, Toshiaki</creatorcontrib><creatorcontrib>Ofuji, Kazuya</creatorcontrib><creatorcontrib>Yoshimura, Mayuko</creatorcontrib><creatorcontrib>Tsuchiya, Nobuhiro</creatorcontrib><creatorcontrib>Takahashi, Mari</creatorcontrib><creatorcontrib>Nobuoka, Daisuke</creatorcontrib><creatorcontrib>Gotohda, Naoto</creatorcontrib><creatorcontrib>Takahashi, Shinichiro</creatorcontrib><creatorcontrib>Kato, Yuichiro</creatorcontrib><creatorcontrib>Konishi, Masaru</creatorcontrib><creatorcontrib>Kinoshita, Taira</creatorcontrib><creatorcontrib>Ikeda, Masafumi</creatorcontrib><creatorcontrib>Nakachi, Kohei</creatorcontrib><creatorcontrib>Yamazaki, Naoya</creatorcontrib><creatorcontrib>Mizuno, Shoichi</creatorcontrib><creatorcontrib>Takayama, Tadatoshi</creatorcontrib><creatorcontrib>Yamao, Kenji</creatorcontrib><creatorcontrib>Uesaka, Katsuhiko</creatorcontrib><creatorcontrib>Furuse, Junji</creatorcontrib><creatorcontrib>Endo, Itaru</creatorcontrib><creatorcontrib>Nakatsura, Tetsuya</creatorcontrib><collection>Taylor &amp; Francis Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oncoimmunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sawada, Yu</au><au>Yoshikawa, Toshiaki</au><au>Ofuji, Kazuya</au><au>Yoshimura, Mayuko</au><au>Tsuchiya, Nobuhiro</au><au>Takahashi, Mari</au><au>Nobuoka, Daisuke</au><au>Gotohda, Naoto</au><au>Takahashi, Shinichiro</au><au>Kato, Yuichiro</au><au>Konishi, Masaru</au><au>Kinoshita, Taira</au><au>Ikeda, Masafumi</au><au>Nakachi, Kohei</au><au>Yamazaki, Naoya</au><au>Mizuno, Shoichi</au><au>Takayama, Tadatoshi</au><au>Yamao, Kenji</au><au>Uesaka, Katsuhiko</au><au>Furuse, Junji</au><au>Endo, Itaru</au><au>Nakatsura, Tetsuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients</atitle><jtitle>Oncoimmunology</jtitle><addtitle>Oncoimmunology</addtitle><date>2016-05-03</date><risdate>2016</risdate><volume>5</volume><issue>5</issue><spage>e1129483</spage><epage>e1129483</epage><pages>e1129483-e1129483</pages><issn>2162-4011</issn><issn>2162-402X</issn><eissn>2162-402X</eissn><abstract>The recurrence rates of Hepatocellular carcinoma (HCC) are high, necessitating novel and effective adjuvant therapies. Therefore, we conducted a phase II study of glypican-3 (GPC3) peptide vaccine as an adjuvant therapy for HCC patients. Forty-one patients with initial HCC who had undergone surgery or radiofrequency ablation (RFA) were analyzed in this phase II, open-label, single-arm trial. Ten vaccinations were performed for 1 y after curative treatment. We also investigated case-control subjects, where selected patients treated surgically during the same period were analyzed. The expression of GPC3 in the available primary tumors was determined by immunohistochemical analysis. Six patients received RFA therapy while 35 received surgery. The recurrence rate tended to be lower in the 35 patients treated with surgery plus vaccination compared to 33 patients who underwent surgery alone (28.6% vs. 54.3% and 39.4% vs. 54.5% at 1 and 2 y, respectively; p = 0.346, 0.983). Twenty-five patients treated with surgery and vaccination had GPC3-positive tumors; the recurrence rate in this group was significantly lower compared to that in 21 GPC3-positive patients who received surgery only (24% vs. 48% and 52.4% vs. 61.9% at 1 and 2 y, respectively; p = 0.047, 0.387). The GPC3 peptide vaccine improved the 1-y recurrence rate in patients with GPC3-positive tumors. This study demonstrated that GPC3 expression by the primary tumor may be used as a biomarker in a putative larger randomized clinical trial to determine the efficacy of the GPC3-derived peptide vaccine.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>27467945</pmid><doi>10.1080/2162402X.2015.1129483</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2162-4011
ispartof Oncoimmunology, 2016-05, Vol.5 (5), p.e1129483-e1129483
issn 2162-4011
2162-402X
2162-402X
language eng
recordid cdi_proquest_miscellaneous_1807897039
source PubMed Central
subjects Adjuvant therapy
CTL
glypican-3
HCC
Original Research
peptide vaccine
title Phase II study of the GPC3-derived peptide vaccine as an adjuvant therapy for hepatocellular carcinoma patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T21%3A05%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phase%20II%20study%20of%20the%20GPC3-derived%20peptide%20vaccine%20as%20an%20adjuvant%20therapy%20for%20hepatocellular%20carcinoma%20patients&rft.jtitle=Oncoimmunology&rft.au=Sawada,%20Yu&rft.date=2016-05-03&rft.volume=5&rft.issue=5&rft.spage=e1129483&rft.epage=e1129483&rft.pages=e1129483-e1129483&rft.issn=2162-4011&rft.eissn=2162-402X&rft_id=info:doi/10.1080/2162402X.2015.1129483&rft_dat=%3Cproquest_infor%3E1807897039%3C/proquest_infor%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1807897039&rft_id=info:pmid/27467945&rfr_iscdi=true