Cross-reactivity of ten anti-prostate-specific antigen monoclonal antibodies with human glandular kallikrein

Prostate-specific antigen (PSA) is commonly used as a marker for prostate disease. Prostate epithelium expresses both PSA and human glandular kallikrein (hK2) proteins, which share 80% sequence homology. The immunologic cross-reactivity of these two proteins could potentially interfere with determin...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 1997-10, Vol.50 (4), p.567-572
Hauptverfasser: Corey, Eva, Buhler, Kent R., Vessella, Robert L.
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Buhler, Kent R.
Vessella, Robert L.
description Prostate-specific antigen (PSA) is commonly used as a marker for prostate disease. Prostate epithelium expresses both PSA and human glandular kallikrein (hK2) proteins, which share 80% sequence homology. The immunologic cross-reactivity of these two proteins could potentially interfere with determination of PSA levels in diagnoses of prostate cancer. We set out to determine the extent of this cross-reactivity for a panel of 10 anti-PSA monoclonal antibodies (mAbs). Enzyme-linked immunosorbent assay (ELISA), sandwich assays, and western transfer techniques were used to assess the PSA/hK2 cross-reactivity of the anti-PSA mAbs. We did not detect the hK2 protein with any of the 10 anti-PSA mAbs under western transfer conditions. In ELISA experiments, 8 of 10 mAbs exhibited hK2 cross-reactivity under certain conditions. However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of the PSA signal. We have evaluated 10 anti-PSA mAbs and determined that despite the 80% homology between However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of th PSA and hK2 proteins, cross-reactivity with hK2 by these antibodies would not significantly affect the determination of PSA levels by means of sandwich assays.
doi_str_mv 10.1016/S0090-4295(97)00415-9
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Prostate epithelium expresses both PSA and human glandular kallikrein (hK2) proteins, which share 80% sequence homology. The immunologic cross-reactivity of these two proteins could potentially interfere with determination of PSA levels in diagnoses of prostate cancer. We set out to determine the extent of this cross-reactivity for a panel of 10 anti-PSA monoclonal antibodies (mAbs). Enzyme-linked immunosorbent assay (ELISA), sandwich assays, and western transfer techniques were used to assess the PSA/hK2 cross-reactivity of the anti-PSA mAbs. We did not detect the hK2 protein with any of the 10 anti-PSA mAbs under western transfer conditions. In ELISA experiments, 8 of 10 mAbs exhibited hK2 cross-reactivity under certain conditions. However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of the PSA signal. We have evaluated 10 anti-PSA mAbs and determined that despite the 80% homology between However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of th PSA and hK2 proteins, cross-reactivity with hK2 by these antibodies would not significantly affect the determination of PSA levels by means of sandwich assays.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/S0090-4295(97)00415-9</identifier><identifier>PMID: 9338733</identifier><identifier>CODEN: URGYAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Antibodies, Monoclonal - immunology ; Biological and medical sciences ; Cross Reactions ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Kallikreins - immunology ; Medical sciences ; Nephrology. Urinary tract diseases ; Pathology. Cytology. Biochemistry. Spectrometry. 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Prostate epithelium expresses both PSA and human glandular kallikrein (hK2) proteins, which share 80% sequence homology. The immunologic cross-reactivity of these two proteins could potentially interfere with determination of PSA levels in diagnoses of prostate cancer. We set out to determine the extent of this cross-reactivity for a panel of 10 anti-PSA monoclonal antibodies (mAbs). Enzyme-linked immunosorbent assay (ELISA), sandwich assays, and western transfer techniques were used to assess the PSA/hK2 cross-reactivity of the anti-PSA mAbs. We did not detect the hK2 protein with any of the 10 anti-PSA mAbs under western transfer conditions. In ELISA experiments, 8 of 10 mAbs exhibited hK2 cross-reactivity under certain conditions. However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of the PSA signal. We have evaluated 10 anti-PSA mAbs and determined that despite the 80% homology between However, no combination of mAbs tested in sandwich assays exhibited a signal in hK2 cross-reactivity experiments greater than 0.1 % of th PSA and hK2 proteins, cross-reactivity with hK2 by these antibodies would not significantly affect the determination of PSA levels by means of sandwich assays.</description><subject>Antibodies, Monoclonal - immunology</subject><subject>Biological and medical sciences</subject><subject>Cross Reactions</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Kallikreins - immunology</subject><subject>Medical sciences</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Prostate-Specific Antigen - immunology</subject><subject>Tumors of the urinary system</subject><subject>Urinary system</subject><subject>Urinary tract. 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Urinary tract diseases</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Prostate-Specific Antigen - immunology</topic><topic>Tumors of the urinary system</topic><topic>Urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Corey, Eva</creatorcontrib><creatorcontrib>Buhler, Kent R.</creatorcontrib><creatorcontrib>Vessella, Robert L.</creatorcontrib><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>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Corey, Eva</au><au>Buhler, Kent R.</au><au>Vessella, Robert L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cross-reactivity of ten anti-prostate-specific antigen monoclonal antibodies with human glandular kallikrein</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>1997-10-01</date><risdate>1997</risdate><volume>50</volume><issue>4</issue><spage>567</spage><epage>572</epage><pages>567-572</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>Prostate-specific antigen (PSA) is commonly used as a marker for prostate disease. 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subjects Antibodies, Monoclonal - immunology
Biological and medical sciences
Cross Reactions
Humans
Investigative techniques, diagnostic techniques (general aspects)
Kallikreins - immunology
Medical sciences
Nephrology. Urinary tract diseases
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Prostate-Specific Antigen - immunology
Tumors of the urinary system
Urinary system
Urinary tract. Prostate gland
title Cross-reactivity of ten anti-prostate-specific antigen monoclonal antibodies with human glandular kallikrein
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