Loading…
Clinical Development of Immune Checkpoint Inhibitors
Recent progress in cancer immunotherapy has been remarkable. Most striking are the clinical development and approval of immunomodulators, also known as immune checkpoint inhibitors. These monoclonal antibodies (mAb) are directed to immune checkpoint molecules, which are expressed on immune cells and...
Saved in:
Published in: | BioMed research international 2015-01, Vol.2015 (2015), p.1-12 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73 |
---|---|
cites | cdi_FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73 |
container_end_page | 12 |
container_issue | 2015 |
container_start_page | 1 |
container_title | BioMed research international |
container_volume | 2015 |
creator | Kitano, Shigehisa Tada, Kohei Kondo, Shunsuke Ito, Ayumu |
description | Recent progress in cancer immunotherapy has been remarkable. Most striking are the clinical development and approval of immunomodulators, also known as immune checkpoint inhibitors. These monoclonal antibodies (mAb) are directed to immune checkpoint molecules, which are expressed on immune cells and mediate signals to attenuate excessive immune reactions. Although mAbs targeting tumor associated antigens, such as anti-CD20 mAb and anti-Her2 mAb, directly recognize tumor cells and induce cell death, immune checkpoint inhibitors restore and augment the antitumor immune activities of cytotoxic T cells by blocking immune checkpoint molecules on T cells or their ligands on antigen presenting and tumor cells. Based on preclinical data, many clinical trials have demonstrated the acceptable safety profiles and efficacies of immune checkpoint inhibitors in a variety of cancers. The first in class approved immune checkpoint inhibitor is ipilimumab, an anti-CTLA-4 (cytotoxic T lymphocyte antigen-4) mAb. Two pivotal phase III randomized controlled trials demonstrated a survival benefit in patients with metastatic melanoma. In 2011, the US Food and Drug Administration (FDA) approved ipilimumab for metastatic melanoma. Several clinical trials have since investigated new agents, alone and in combination, for various cancers. In this review, we discuss the current development status of and future challenges in utilizing immune checkpoint inhibitors. |
doi_str_mv | 10.1155/2015/605478 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4486755</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A458162163</galeid><sourcerecordid>A458162163</sourcerecordid><originalsourceid>FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73</originalsourceid><addsrcrecordid>eNqN0s1P2zAYBnBrGhoV9MR9qsRlApX6jb-Sy6SqG1ulSlzgbDnJa2pI7BI3Rfvv56isg11GLrbinx457xNCzoBeAQgxyyiImaSCq_wDGWUM-FQCh4-HPWPHZBzjA01PDpIW8hM5ziQkRdWI8EXjvKtMM_mGO2zCpkW_nQQ7WbZt73GyWGP1uAkuvVz6tSvdNnTxlBxZ00Qcv6wn5O76--3i53R182O5mK-mlSj4dqok1MqWmbSM5jWvBebWGoNQ2BwUMwqyOiuNBJWZorZCWVoi5FIYM-wUOyFf97mbvmyxrtLVOtPoTeda0_3SwTj99sS7tb4PO815LpUQKeDLS0AXnnqMW926WGHTGI-hjxpUGh_lnNH_U1kIJSkVRaLn_9CH0Hc-TWJQIKSiVP5V96ZB7bwN6YrVEKrnXKQqMpAsqcu9qroQY4f28HVA9dCwHhrW-4aT_vx6IAf7p88ELvZg7Xxtnt370jARtOYVFulHydlvSHS05A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1691567006</pqid></control><display><type>article</type><title>Clinical Development of Immune Checkpoint Inhibitors</title><source>Access via ProQuest (Open Access)</source><source>Wiley Online Library Open Access</source><creator>Kitano, Shigehisa ; Tada, Kohei ; Kondo, Shunsuke ; Ito, Ayumu</creator><contributor>Zubair, Swaleha</contributor><creatorcontrib>Kitano, Shigehisa ; Tada, Kohei ; Kondo, Shunsuke ; Ito, Ayumu ; Zubair, Swaleha</creatorcontrib><description>Recent progress in cancer immunotherapy has been remarkable. Most striking are the clinical development and approval of immunomodulators, also known as immune checkpoint inhibitors. These monoclonal antibodies (mAb) are directed to immune checkpoint molecules, which are expressed on immune cells and mediate signals to attenuate excessive immune reactions. Although mAbs targeting tumor associated antigens, such as anti-CD20 mAb and anti-Her2 mAb, directly recognize tumor cells and induce cell death, immune checkpoint inhibitors restore and augment the antitumor immune activities of cytotoxic T cells by blocking immune checkpoint molecules on T cells or their ligands on antigen presenting and tumor cells. Based on preclinical data, many clinical trials have demonstrated the acceptable safety profiles and efficacies of immune checkpoint inhibitors in a variety of cancers. The first in class approved immune checkpoint inhibitor is ipilimumab, an anti-CTLA-4 (cytotoxic T lymphocyte antigen-4) mAb. Two pivotal phase III randomized controlled trials demonstrated a survival benefit in patients with metastatic melanoma. In 2011, the US Food and Drug Administration (FDA) approved ipilimumab for metastatic melanoma. Several clinical trials have since investigated new agents, alone and in combination, for various cancers. In this review, we discuss the current development status of and future challenges in utilizing immune checkpoint inhibitors.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2015/605478</identifier><identifier>PMID: 26161407</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Apoptosis ; Biomarkers ; Biomarkers, Tumor - metabolism ; Cancer ; Cancer therapies ; Care and treatment ; Chemotherapy ; Clinical trials ; CTLA-4 Antigen - immunology ; Drug Therapy, Combination ; Gene expression ; Homeostasis ; Humans ; Immune response ; Immunotherapy ; Immunotherapy - adverse effects ; Ligands ; Lymphocytes ; Melanoma ; Metastasis ; Methods ; Neoplasms - immunology ; Neoplasms - therapy ; Observations ; Oncology ; Pharmaceutical industry ; Programmed Cell Death 1 Receptor - immunology ; Prostate cancer ; Review ; T cell receptors</subject><ispartof>BioMed research international, 2015-01, Vol.2015 (2015), p.1-12</ispartof><rights>Copyright © 2015 Ayumu Ito et al.</rights><rights>COPYRIGHT 2015 John Wiley & Sons, Inc.</rights><rights>Copyright © 2015 Ayumu Ito et al. Ayumu Ito et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2015 Ayumu Ito et al. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73</citedby><cites>FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73</cites><orcidid>0000-0001-5681-6357 ; 0000-0002-4041-8298</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1691567006/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1691567006?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26161407$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zubair, Swaleha</contributor><creatorcontrib>Kitano, Shigehisa</creatorcontrib><creatorcontrib>Tada, Kohei</creatorcontrib><creatorcontrib>Kondo, Shunsuke</creatorcontrib><creatorcontrib>Ito, Ayumu</creatorcontrib><title>Clinical Development of Immune Checkpoint Inhibitors</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Recent progress in cancer immunotherapy has been remarkable. Most striking are the clinical development and approval of immunomodulators, also known as immune checkpoint inhibitors. These monoclonal antibodies (mAb) are directed to immune checkpoint molecules, which are expressed on immune cells and mediate signals to attenuate excessive immune reactions. Although mAbs targeting tumor associated antigens, such as anti-CD20 mAb and anti-Her2 mAb, directly recognize tumor cells and induce cell death, immune checkpoint inhibitors restore and augment the antitumor immune activities of cytotoxic T cells by blocking immune checkpoint molecules on T cells or their ligands on antigen presenting and tumor cells. Based on preclinical data, many clinical trials have demonstrated the acceptable safety profiles and efficacies of immune checkpoint inhibitors in a variety of cancers. The first in class approved immune checkpoint inhibitor is ipilimumab, an anti-CTLA-4 (cytotoxic T lymphocyte antigen-4) mAb. Two pivotal phase III randomized controlled trials demonstrated a survival benefit in patients with metastatic melanoma. In 2011, the US Food and Drug Administration (FDA) approved ipilimumab for metastatic melanoma. Several clinical trials have since investigated new agents, alone and in combination, for various cancers. In this review, we discuss the current development status of and future challenges in utilizing immune checkpoint inhibitors.</description><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>CTLA-4 Antigen - immunology</subject><subject>Drug Therapy, Combination</subject><subject>Gene expression</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunotherapy</subject><subject>Immunotherapy - adverse effects</subject><subject>Ligands</subject><subject>Lymphocytes</subject><subject>Melanoma</subject><subject>Metastasis</subject><subject>Methods</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - therapy</subject><subject>Observations</subject><subject>Oncology</subject><subject>Pharmaceutical industry</subject><subject>Programmed Cell Death 1 Receptor - immunology</subject><subject>Prostate cancer</subject><subject>Review</subject><subject>T cell receptors</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqN0s1P2zAYBnBrGhoV9MR9qsRlApX6jb-Sy6SqG1ulSlzgbDnJa2pI7BI3Rfvv56isg11GLrbinx457xNCzoBeAQgxyyiImaSCq_wDGWUM-FQCh4-HPWPHZBzjA01PDpIW8hM5ziQkRdWI8EXjvKtMM_mGO2zCpkW_nQQ7WbZt73GyWGP1uAkuvVz6tSvdNnTxlBxZ00Qcv6wn5O76--3i53R182O5mK-mlSj4dqok1MqWmbSM5jWvBebWGoNQ2BwUMwqyOiuNBJWZorZCWVoi5FIYM-wUOyFf97mbvmyxrtLVOtPoTeda0_3SwTj99sS7tb4PO815LpUQKeDLS0AXnnqMW926WGHTGI-hjxpUGh_lnNH_U1kIJSkVRaLn_9CH0Hc-TWJQIKSiVP5V96ZB7bwN6YrVEKrnXKQqMpAsqcu9qroQY4f28HVA9dCwHhrW-4aT_vx6IAf7p88ELvZg7Xxtnt370jARtOYVFulHydlvSHS05A</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Kitano, Shigehisa</creator><creator>Tada, Kohei</creator><creator>Kondo, Shunsuke</creator><creator>Ito, Ayumu</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>3V.</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7T5</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5681-6357</orcidid><orcidid>https://orcid.org/0000-0002-4041-8298</orcidid></search><sort><creationdate>20150101</creationdate><title>Clinical Development of Immune Checkpoint Inhibitors</title><author>Kitano, Shigehisa ; Tada, Kohei ; Kondo, Shunsuke ; Ito, Ayumu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Apoptosis</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>CTLA-4 Antigen - immunology</topic><topic>Drug Therapy, Combination</topic><topic>Gene expression</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunotherapy</topic><topic>Immunotherapy - adverse effects</topic><topic>Ligands</topic><topic>Lymphocytes</topic><topic>Melanoma</topic><topic>Metastasis</topic><topic>Methods</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - therapy</topic><topic>Observations</topic><topic>Oncology</topic><topic>Pharmaceutical industry</topic><topic>Programmed Cell Death 1 Receptor - immunology</topic><topic>Prostate cancer</topic><topic>Review</topic><topic>T cell receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kitano, Shigehisa</creatorcontrib><creatorcontrib>Tada, Kohei</creatorcontrib><creatorcontrib>Kondo, Shunsuke</creatorcontrib><creatorcontrib>Ito, Ayumu</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Middle East & Africa Database</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Access via ProQuest (Open Access)</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>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitano, Shigehisa</au><au>Tada, Kohei</au><au>Kondo, Shunsuke</au><au>Ito, Ayumu</au><au>Zubair, Swaleha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical Development of Immune Checkpoint Inhibitors</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>2015</volume><issue>2015</issue><spage>1</spage><epage>12</epage><pages>1-12</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Recent progress in cancer immunotherapy has been remarkable. Most striking are the clinical development and approval of immunomodulators, also known as immune checkpoint inhibitors. These monoclonal antibodies (mAb) are directed to immune checkpoint molecules, which are expressed on immune cells and mediate signals to attenuate excessive immune reactions. Although mAbs targeting tumor associated antigens, such as anti-CD20 mAb and anti-Her2 mAb, directly recognize tumor cells and induce cell death, immune checkpoint inhibitors restore and augment the antitumor immune activities of cytotoxic T cells by blocking immune checkpoint molecules on T cells or their ligands on antigen presenting and tumor cells. Based on preclinical data, many clinical trials have demonstrated the acceptable safety profiles and efficacies of immune checkpoint inhibitors in a variety of cancers. The first in class approved immune checkpoint inhibitor is ipilimumab, an anti-CTLA-4 (cytotoxic T lymphocyte antigen-4) mAb. Two pivotal phase III randomized controlled trials demonstrated a survival benefit in patients with metastatic melanoma. In 2011, the US Food and Drug Administration (FDA) approved ipilimumab for metastatic melanoma. Several clinical trials have since investigated new agents, alone and in combination, for various cancers. In this review, we discuss the current development status of and future challenges in utilizing immune checkpoint inhibitors.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>26161407</pmid><doi>10.1155/2015/605478</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-5681-6357</orcidid><orcidid>https://orcid.org/0000-0002-4041-8298</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-6133 |
ispartof | BioMed research international, 2015-01, Vol.2015 (2015), p.1-12 |
issn | 2314-6133 2314-6141 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4486755 |
source | Access via ProQuest (Open Access); Wiley Online Library Open Access |
subjects | Apoptosis Biomarkers Biomarkers, Tumor - metabolism Cancer Cancer therapies Care and treatment Chemotherapy Clinical trials CTLA-4 Antigen - immunology Drug Therapy, Combination Gene expression Homeostasis Humans Immune response Immunotherapy Immunotherapy - adverse effects Ligands Lymphocytes Melanoma Metastasis Methods Neoplasms - immunology Neoplasms - therapy Observations Oncology Pharmaceutical industry Programmed Cell Death 1 Receptor - immunology Prostate cancer Review T cell receptors |
title | Clinical Development of Immune Checkpoint Inhibitors |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T10%3A22%3A17IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20Development%20of%20Immune%20Checkpoint%20Inhibitors&rft.jtitle=BioMed%20research%20international&rft.au=Kitano,%20Shigehisa&rft.date=2015-01-01&rft.volume=2015&rft.issue=2015&rft.spage=1&rft.epage=12&rft.pages=1-12&rft.issn=2314-6133&rft.eissn=2314-6141&rft_id=info:doi/10.1155/2015/605478&rft_dat=%3Cgale_pubme%3EA458162163%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c594t-761d7fb26f308d4d5e8ffaae19f8173a712d2ba6172a9df57f0be1865aaf0be73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1691567006&rft_id=info:pmid/26161407&rft_galeid=A458162163&rfr_iscdi=true |