Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells

HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of immunology (1950) 1986-06, Vol.136 (11), p.4311-4318
Hauptverfasser: Pesando, JM, Graf, L
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4318
container_issue 11
container_start_page 4311
container_title The Journal of immunology (1950)
container_volume 136
creator Pesando, JM
Graf, L
description HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive malignant B cell populations and autologous normal B cell lines. Forty additional HLA class II-specific MoAb were also tested for their ability to bind to these cells. By using indirect immunofluorescence and immune precipitation assays, we find that malignant B cells often fail to express one or more of the three known types of HLA class II antigens. Cell lines with the following five phenotypes have been identified: HLA-DR+, -DQ+, -DP+; HLA-DR+, -DQ-, -DP+; HLA-DR-, -DQ+, -DP+; HLA-DR-, -DQ-, -DP+; and HLA-DR-, -DQ-, -DP-. These cell lines have been used to characterize the subregion specificity of MoAb that react with HLA class II antigens. This work confirms the existence of complicated patterns of serologic cross-reactivity between the three different types of HLA class II molecules. It also increases our understanding of the specificity of individual MoAb, thereby facilitating future investigation of the distribution and function of individual antigens. Our studies are consistent with the proposal that altered expression of HLA antigens on tumors might impair recognition of these cells by the immune system of the host, thereby contributing to the proliferation of a malignant clone.
doi_str_mv 10.4049/jimmunol.136.11.4311
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76809488</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76809488</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3251-c2e995f0c6d4d71f909b3f27457b0630360627f5a8e9760220a4b19b5de3a6643</originalsourceid><addsrcrecordid>eNpNkE1PGzEQhi1UREPgH1BpD1XVQzbM2F57fUwTWpBStUVwtry7djDaj2AnSvvv6ygBcRrL88zMq4eQK4QpB66un33XbfuhnSITU8QpZ4gnZIRFAbkQID6QEQClOUohP5LzGJ8BQADlZ-SMKqaQ44j8XHjnbLD9xps2s3_Xwcbohz4bXHa7nOWL-0mWL_5MMtM36fE71Y1f2T5mielM61d9-sm-ZbVt23hBTp1po7081jF5_H7zML_Nl79-3M1ny7xmtMC8plapwkEtGt5IdApUxRyVvJAVCAYspafSFaa0SqbEFAyvUFVFY5kRgrMx-XLYuw7Dy9bGje583CcwvR22UUtRguJlmUB-AOswxBis0-vgOxP-aQS9t6hfLepkUSPqvcU09um4f1t1tnkbOmpL_c_Hvom1aV0wfe3jG1ZK4FTRhH09YE9-9bTzweqYlLVpKerdbvf-4n91gobb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76809488</pqid></control><display><type>article</type><title>Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Pesando, JM ; Graf, L</creator><creatorcontrib>Pesando, JM ; Graf, L</creatorcontrib><description>HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive malignant B cell populations and autologous normal B cell lines. Forty additional HLA class II-specific MoAb were also tested for their ability to bind to these cells. By using indirect immunofluorescence and immune precipitation assays, we find that malignant B cells often fail to express one or more of the three known types of HLA class II antigens. Cell lines with the following five phenotypes have been identified: HLA-DR+, -DQ+, -DP+; HLA-DR+, -DQ-, -DP+; HLA-DR-, -DQ+, -DP+; HLA-DR-, -DQ-, -DP+; and HLA-DR-, -DQ-, -DP-. These cell lines have been used to characterize the subregion specificity of MoAb that react with HLA class II antigens. This work confirms the existence of complicated patterns of serologic cross-reactivity between the three different types of HLA class II molecules. It also increases our understanding of the specificity of individual MoAb, thereby facilitating future investigation of the distribution and function of individual antigens. Our studies are consistent with the proposal that altered expression of HLA antigens on tumors might impair recognition of these cells by the immune system of the host, thereby contributing to the proliferation of a malignant clone.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.136.11.4311</identifier><identifier>PMID: 2939141</identifier><identifier>CODEN: JOIMA3</identifier><language>eng</language><publisher>Bethesda, MD: Am Assoc Immnol</publisher><subject>Antibodies, Monoclonal ; Antigens, Neoplasm - analysis ; Antigens, Neoplasm - immunology ; B-Lymphocytes - immunology ; Binding Sites, Antibody ; Biological and medical sciences ; Cell Line ; Hematologic and hematopoietic diseases ; Histocompatibility Antigens Class II - analysis ; Histocompatibility Antigens Class II - immunology ; HLA-DP Antigens ; HLA-DQ Antigens ; HLA-DR Antigens ; Humans ; Leukemia, Lymphoid - immunology ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphoma - immunology ; Medical sciences ; Neprilysin</subject><ispartof>The Journal of immunology (1950), 1986-06, Vol.136 (11), p.4311-4318</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3251-c2e995f0c6d4d71f909b3f27457b0630360627f5a8e9760220a4b19b5de3a6643</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8704292$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2939141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pesando, JM</creatorcontrib><creatorcontrib>Graf, L</creatorcontrib><title>Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive malignant B cell populations and autologous normal B cell lines. Forty additional HLA class II-specific MoAb were also tested for their ability to bind to these cells. By using indirect immunofluorescence and immune precipitation assays, we find that malignant B cells often fail to express one or more of the three known types of HLA class II antigens. Cell lines with the following five phenotypes have been identified: HLA-DR+, -DQ+, -DP+; HLA-DR+, -DQ-, -DP+; HLA-DR-, -DQ+, -DP+; HLA-DR-, -DQ-, -DP+; and HLA-DR-, -DQ-, -DP-. These cell lines have been used to characterize the subregion specificity of MoAb that react with HLA class II antigens. This work confirms the existence of complicated patterns of serologic cross-reactivity between the three different types of HLA class II molecules. It also increases our understanding of the specificity of individual MoAb, thereby facilitating future investigation of the distribution and function of individual antigens. Our studies are consistent with the proposal that altered expression of HLA antigens on tumors might impair recognition of these cells by the immune system of the host, thereby contributing to the proliferation of a malignant clone.</description><subject>Antibodies, Monoclonal</subject><subject>Antigens, Neoplasm - analysis</subject><subject>Antigens, Neoplasm - immunology</subject><subject>B-Lymphocytes - immunology</subject><subject>Binding Sites, Antibody</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Histocompatibility Antigens Class II - analysis</subject><subject>Histocompatibility Antigens Class II - immunology</subject><subject>HLA-DP Antigens</subject><subject>HLA-DQ Antigens</subject><subject>HLA-DR Antigens</subject><subject>Humans</subject><subject>Leukemia, Lymphoid - immunology</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphoma - immunology</subject><subject>Medical sciences</subject><subject>Neprilysin</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1PGzEQhi1UREPgH1BpD1XVQzbM2F57fUwTWpBStUVwtry7djDaj2AnSvvv6ygBcRrL88zMq4eQK4QpB66un33XbfuhnSITU8QpZ4gnZIRFAbkQID6QEQClOUohP5LzGJ8BQADlZ-SMKqaQ44j8XHjnbLD9xps2s3_Xwcbohz4bXHa7nOWL-0mWL_5MMtM36fE71Y1f2T5mielM61d9-sm-ZbVt23hBTp1po7081jF5_H7zML_Nl79-3M1ny7xmtMC8plapwkEtGt5IdApUxRyVvJAVCAYspafSFaa0SqbEFAyvUFVFY5kRgrMx-XLYuw7Dy9bGje583CcwvR22UUtRguJlmUB-AOswxBis0-vgOxP-aQS9t6hfLepkUSPqvcU09um4f1t1tnkbOmpL_c_Hvom1aV0wfe3jG1ZK4FTRhH09YE9-9bTzweqYlLVpKerdbvf-4n91gobb</recordid><startdate>19860601</startdate><enddate>19860601</enddate><creator>Pesando, JM</creator><creator>Graf, L</creator><general>Am Assoc Immnol</general><general>American Association of Immunologists</general><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>19860601</creationdate><title>Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells</title><author>Pesando, JM ; Graf, L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3251-c2e995f0c6d4d71f909b3f27457b0630360627f5a8e9760220a4b19b5de3a6643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Antibodies, Monoclonal</topic><topic>Antigens, Neoplasm - analysis</topic><topic>Antigens, Neoplasm - immunology</topic><topic>B-Lymphocytes - immunology</topic><topic>Binding Sites, Antibody</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Histocompatibility Antigens Class II - analysis</topic><topic>Histocompatibility Antigens Class II - immunology</topic><topic>HLA-DP Antigens</topic><topic>HLA-DQ Antigens</topic><topic>HLA-DR Antigens</topic><topic>Humans</topic><topic>Leukemia, Lymphoid - immunology</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Lymphoma - immunology</topic><topic>Medical sciences</topic><topic>Neprilysin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pesando, JM</creatorcontrib><creatorcontrib>Graf, 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>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pesando, JM</au><au>Graf, L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1986-06-01</date><risdate>1986</risdate><volume>136</volume><issue>11</issue><spage>4311</spage><epage>4318</epage><pages>4311-4318</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><coden>JOIMA3</coden><abstract>HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive malignant B cell populations and autologous normal B cell lines. Forty additional HLA class II-specific MoAb were also tested for their ability to bind to these cells. By using indirect immunofluorescence and immune precipitation assays, we find that malignant B cells often fail to express one or more of the three known types of HLA class II antigens. Cell lines with the following five phenotypes have been identified: HLA-DR+, -DQ+, -DP+; HLA-DR+, -DQ-, -DP+; HLA-DR-, -DQ+, -DP+; HLA-DR-, -DQ-, -DP+; and HLA-DR-, -DQ-, -DP-. These cell lines have been used to characterize the subregion specificity of MoAb that react with HLA class II antigens. This work confirms the existence of complicated patterns of serologic cross-reactivity between the three different types of HLA class II molecules. It also increases our understanding of the specificity of individual MoAb, thereby facilitating future investigation of the distribution and function of individual antigens. Our studies are consistent with the proposal that altered expression of HLA antigens on tumors might impair recognition of these cells by the immune system of the host, thereby contributing to the proliferation of a malignant clone.</abstract><cop>Bethesda, MD</cop><pub>Am Assoc Immnol</pub><pmid>2939141</pmid><doi>10.4049/jimmunol.136.11.4311</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 1986-06, Vol.136 (11), p.4311-4318
issn 0022-1767
1550-6606
language eng
recordid cdi_proquest_miscellaneous_76809488
source MEDLINE; Alma/SFX Local Collection
subjects Antibodies, Monoclonal
Antigens, Neoplasm - analysis
Antigens, Neoplasm - immunology
B-Lymphocytes - immunology
Binding Sites, Antibody
Biological and medical sciences
Cell Line
Hematologic and hematopoietic diseases
Histocompatibility Antigens Class II - analysis
Histocompatibility Antigens Class II - immunology
HLA-DP Antigens
HLA-DQ Antigens
HLA-DR Antigens
Humans
Leukemia, Lymphoid - immunology
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Lymphoma - immunology
Medical sciences
Neprilysin
title Differential expression of HLA-DR, -DQ, and -DP antigens on malignant B cells
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T08%3A07%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20expression%20of%20HLA-DR,%20-DQ,%20and%20-DP%20antigens%20on%20malignant%20B%20cells&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Pesando,%20JM&rft.date=1986-06-01&rft.volume=136&rft.issue=11&rft.spage=4311&rft.epage=4318&rft.pages=4311-4318&rft.issn=0022-1767&rft.eissn=1550-6606&rft.coden=JOIMA3&rft_id=info:doi/10.4049/jimmunol.136.11.4311&rft_dat=%3Cproquest_cross%3E76809488%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=76809488&rft_id=info:pmid/2939141&rfr_iscdi=true