Anti-ALK Antibodies in Patients with ALK-Positive Malignancies Not Expressing NPM-ALK
Patients with Nucleophosmin (NPM)- Anaplastic Lymphoma Kinase (ALK) fusion positive Anaplastic Large Cell Lymphoma produce autoantibodies against ALK indicative of an immune response against epitopes of the chimeric fusion protein. We asked whether ALK-expression in other malignancies induces specif...
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Veröffentlicht in: | Journal of Cancer 2016-01, Vol.7 (11), p.1383-1387 |
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creator | Damm-Welk, Christine Siddiqi, Faraz Fischer, Matthias Hero, Barbara Narayanan, Vignesh Camidge, David Ross Harris, Michael Burke, Amos Lehrnbecher, Thomas Pulford, Karen Oschlies, Ilske Siebert, Reiner Turner, Suzanne Woessmann, Wilhelm |
description | Patients with Nucleophosmin (NPM)- Anaplastic Lymphoma Kinase (ALK) fusion positive Anaplastic Large Cell Lymphoma produce autoantibodies against ALK indicative of an immune response against epitopes of the chimeric fusion protein. We asked whether ALK-expression in other malignancies induces specific antibodies. Antibodies against ALK were detected in sera of one of 50 analysed ALK-expressing neuroblastoma patients, 13 of 21 ALK positive non-small cell lung carcinoma (NSCLC) patients, 13 of 22 ALK translocation-positive, but NPM-ALK-negative lymphoma patients and one of one ALK-positive rhabdomyosarcoma patient, but not in 20 healthy adults. These data suggest that boosting a pre-existent anti-ALK immune response may be more feasible for patients with ALK-positive NSCLC, lymphomas and rhabdomyosarcomas than for tumours expressing wild-type ALK. |
doi_str_mv | 10.7150/jca.15238 |
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We asked whether ALK-expression in other malignancies induces specific antibodies. Antibodies against ALK were detected in sera of one of 50 analysed ALK-expressing neuroblastoma patients, 13 of 21 ALK positive non-small cell lung carcinoma (NSCLC) patients, 13 of 22 ALK translocation-positive, but NPM-ALK-negative lymphoma patients and one of one ALK-positive rhabdomyosarcoma patient, but not in 20 healthy adults. These data suggest that boosting a pre-existent anti-ALK immune response may be more feasible for patients with ALK-positive NSCLC, lymphomas and rhabdomyosarcomas than for tumours expressing wild-type ALK.</description><identifier>ISSN: 1837-9664</identifier><identifier>EISSN: 1837-9664</identifier><identifier>DOI: 10.7150/jca.15238</identifier><identifier>PMID: 27471553</identifier><language>eng</language><publisher>Australia: Ivyspring International Publisher</publisher><subject>Short Research Communication</subject><ispartof>Journal of Cancer, 2016-01, Vol.7 (11), p.1383-1387</ispartof><rights>Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. 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We asked whether ALK-expression in other malignancies induces specific antibodies. Antibodies against ALK were detected in sera of one of 50 analysed ALK-expressing neuroblastoma patients, 13 of 21 ALK positive non-small cell lung carcinoma (NSCLC) patients, 13 of 22 ALK translocation-positive, but NPM-ALK-negative lymphoma patients and one of one ALK-positive rhabdomyosarcoma patient, but not in 20 healthy adults. These data suggest that boosting a pre-existent anti-ALK immune response may be more feasible for patients with ALK-positive NSCLC, lymphomas and rhabdomyosarcomas than for tumours expressing wild-type ALK.</description><subject>Short Research Communication</subject><issn>1837-9664</issn><issn>1837-9664</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpVkc1OAjEUhRujEYIsfAHTpS4Gp9N2Ot2YEII_EZCFrJvS6UDJ0OJ0QH17O4IEu-g9yf167k0PANco7jFE4_uVkj1EE5ydgTbKMIt4mpLzE90CXe9XcTiYJ4zgS9AKJbyluA1mfVubqD96hY2Yu9xoD42FU1kbbWsPP029hKEfTZ03tdlpOJalWVhpVYNOXA2HX5tKe2_sAk6m48bsClwUsvS6e6gdMHscvg-eo9Hb08ugP4oUZrSOqNYcMy0LxGhKdJ4hlRBOC6ZwThRnqqCpTonMMI1jhFGe5kGkkvOChTvGHfCw991s52udq7BxJUuxqcxaVt_CSSP-d6xZioXbCcJTghIUDG4PBpX72Gpfi7XxSpeltNptvUBZzDJOGcIBvdujqnLeV7o4jkGxaJIQIQnxm0Rgb073OpJ__45_AEClgvI</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Damm-Welk, Christine</creator><creator>Siddiqi, Faraz</creator><creator>Fischer, Matthias</creator><creator>Hero, Barbara</creator><creator>Narayanan, Vignesh</creator><creator>Camidge, David Ross</creator><creator>Harris, Michael</creator><creator>Burke, Amos</creator><creator>Lehrnbecher, Thomas</creator><creator>Pulford, Karen</creator><creator>Oschlies, Ilske</creator><creator>Siebert, Reiner</creator><creator>Turner, Suzanne</creator><creator>Woessmann, Wilhelm</creator><general>Ivyspring International Publisher</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160101</creationdate><title>Anti-ALK Antibodies in Patients with ALK-Positive Malignancies Not Expressing NPM-ALK</title><author>Damm-Welk, Christine ; Siddiqi, Faraz ; Fischer, Matthias ; Hero, Barbara ; Narayanan, Vignesh ; Camidge, David Ross ; Harris, Michael ; Burke, Amos ; Lehrnbecher, Thomas ; Pulford, Karen ; Oschlies, Ilske ; Siebert, Reiner ; Turner, Suzanne ; Woessmann, Wilhelm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-5ee937eaf17564ed81c2495f7c3d4c97cf56e64a83500131d6d5006a99f76a903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Short Research Communication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Damm-Welk, Christine</creatorcontrib><creatorcontrib>Siddiqi, Faraz</creatorcontrib><creatorcontrib>Fischer, Matthias</creatorcontrib><creatorcontrib>Hero, Barbara</creatorcontrib><creatorcontrib>Narayanan, Vignesh</creatorcontrib><creatorcontrib>Camidge, David Ross</creatorcontrib><creatorcontrib>Harris, Michael</creatorcontrib><creatorcontrib>Burke, Amos</creatorcontrib><creatorcontrib>Lehrnbecher, Thomas</creatorcontrib><creatorcontrib>Pulford, Karen</creatorcontrib><creatorcontrib>Oschlies, Ilske</creatorcontrib><creatorcontrib>Siebert, Reiner</creatorcontrib><creatorcontrib>Turner, Suzanne</creatorcontrib><creatorcontrib>Woessmann, Wilhelm</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Damm-Welk, Christine</au><au>Siddiqi, Faraz</au><au>Fischer, Matthias</au><au>Hero, Barbara</au><au>Narayanan, Vignesh</au><au>Camidge, David Ross</au><au>Harris, Michael</au><au>Burke, Amos</au><au>Lehrnbecher, Thomas</au><au>Pulford, Karen</au><au>Oschlies, Ilske</au><au>Siebert, Reiner</au><au>Turner, Suzanne</au><au>Woessmann, Wilhelm</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-ALK Antibodies in Patients with ALK-Positive Malignancies Not Expressing NPM-ALK</atitle><jtitle>Journal of Cancer</jtitle><addtitle>J Cancer</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>7</volume><issue>11</issue><spage>1383</spage><epage>1387</epage><pages>1383-1387</pages><issn>1837-9664</issn><eissn>1837-9664</eissn><abstract>Patients with Nucleophosmin (NPM)- Anaplastic Lymphoma Kinase (ALK) fusion positive Anaplastic Large Cell Lymphoma produce autoantibodies against ALK indicative of an immune response against epitopes of the chimeric fusion protein. 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title | Anti-ALK Antibodies in Patients with ALK-Positive Malignancies Not Expressing NPM-ALK |
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