CD43 and CD5 antibodies define four normal and neoplastic B‐cell subsets: A three‐color flow cytometric study
CD43 antibodies are best known for identifying normal and neoplastic T cells and a subset of neoplastic B cells in paraffin sections. The frequency of nonneoplastic CD43 + B cells in different reactive settings, the proportion of B‐cell neoplasms with small CD43+ populations, and the relationship of...
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Veröffentlicht in: | Cytometry (New York, N.Y.) N.Y.), 1995-09, Vol.22 (3), p.223-231 |
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description | CD43 antibodies are best known for identifying normal and neoplastic T cells and a subset of neoplastic B cells in paraffin sections. The frequency of nonneoplastic CD43 + B cells in different reactive settings, the proportion of B‐cell neoplasms with small CD43+ populations, and the relationship of CD43+ B cells to CD5+ B cells are less well established. CD43 and CD5 expression on normal and neoplastic CD19 + B cells was therefore studied in 138 specimens using three‐color flow cytometric analysis.
CD43 and CD5 defined four normal B‐cell subsets (CD43 + CD5 +, CD43 + CD5−, CD43−CD5+, and CD43−CD5−). A significantly greater proportion of CD43+ B cells was found in cord blood and putative HIV + blood samples than in normal control bloods. B‐cell neoplasms derived from each of these four B‐cell subsets were identified, with CD43 +/CD5+ and CD43‐/CD5‐ neoplasms being most common. The predominant B‐cell population coexpressed CD43 alone in 2/39 neoplasms and CD5 alone in four. A minority of cases showed heterogeneous CD43 expression. The B cells in two of three posttransplant lymphoproliferative disorders coexpressed CD43. B cells showed weaker CD43 staining than did T‐cells (relative fluorescence 0.38 ± 0.29).
These findings support the concept that CD43 expression by neoplastic B cells is not an aberrant finding. CD43 expression on normal and neoplastic B cells is independent of CD5 expression even though CD43 and CD5 are frequently coexpressed. CD43 expression by B cells sometimes might be underestimated in paraffin sections because it is much weaker than on T cells. Although large discrete populations of CD43+ B cells were only identified in B‐cell neoplasms and posttransplant lymphoproliferative disorders, increased proportions of CD43+ B cells were present in some benign settings. © 1995 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cyto.990220310 |
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CD43 and CD5 defined four normal B‐cell subsets (CD43 + CD5 +, CD43 + CD5−, CD43−CD5+, and CD43−CD5−). A significantly greater proportion of CD43+ B cells was found in cord blood and putative HIV + blood samples than in normal control bloods. B‐cell neoplasms derived from each of these four B‐cell subsets were identified, with CD43 +/CD5+ and CD43‐/CD5‐ neoplasms being most common. The predominant B‐cell population coexpressed CD43 alone in 2/39 neoplasms and CD5 alone in four. A minority of cases showed heterogeneous CD43 expression. The B cells in two of three posttransplant lymphoproliferative disorders coexpressed CD43. B cells showed weaker CD43 staining than did T‐cells (relative fluorescence 0.38 ± 0.29).
These findings support the concept that CD43 expression by neoplastic B cells is not an aberrant finding. CD43 expression on normal and neoplastic B cells is independent of CD5 expression even though CD43 and CD5 are frequently coexpressed. CD43 expression by B cells sometimes might be underestimated in paraffin sections because it is much weaker than on T cells. Although large discrete populations of CD43+ B cells were only identified in B‐cell neoplasms and posttransplant lymphoproliferative disorders, increased proportions of CD43+ B cells were present in some benign settings. © 1995 Wiley‐Liss, Inc.</description><identifier>ISSN: 0196-4763</identifier><identifier>EISSN: 1097-0320</identifier><identifier>DOI: 10.1002/cyto.990220310</identifier><identifier>PMID: 8556954</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Ammonium Chloride ; Animals ; Antibodies - immunology ; Antigens, CD ; Antigens, CD19 - immunology ; B-Lymphocyte Subsets - immunology ; B‐cells ; CD43 ; CD5 ; CD5 Antigens - immunology ; Flow Cytometry ; HIV ; Humans ; immunophenotype ; Leukosialin ; lymphoma ; Lymphoma, B-Cell - immunology ; posttransplant lymphoproliferative disorder ; Reagent Kits, Diagnostic ; Sialoglycoproteins - immunology</subject><ispartof>Cytometry (New York, N.Y.), 1995-09, Vol.22 (3), p.223-231</ispartof><rights>Copyright © 1995 Wiley‐Liss, Inc.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2950-29db0d6b1ce2733c3c401f992a1799111e1785627f4b62eefe0e366804bb5c1b3</citedby><cites>FETCH-LOGICAL-c2950-29db0d6b1ce2733c3c401f992a1799111e1785627f4b62eefe0e366804bb5c1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8556954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lynch, Edward F.</creatorcontrib><creatorcontrib>Jones, Patricia A.</creatorcontrib><creatorcontrib>Swerdlow, Steven H.</creatorcontrib><title>CD43 and CD5 antibodies define four normal and neoplastic B‐cell subsets: A three‐color flow cytometric study</title><title>Cytometry (New York, N.Y.)</title><addtitle>Cytometry</addtitle><description>CD43 antibodies are best known for identifying normal and neoplastic T cells and a subset of neoplastic B cells in paraffin sections. The frequency of nonneoplastic CD43 + B cells in different reactive settings, the proportion of B‐cell neoplasms with small CD43+ populations, and the relationship of CD43+ B cells to CD5+ B cells are less well established. CD43 and CD5 expression on normal and neoplastic CD19 + B cells was therefore studied in 138 specimens using three‐color flow cytometric analysis.
CD43 and CD5 defined four normal B‐cell subsets (CD43 + CD5 +, CD43 + CD5−, CD43−CD5+, and CD43−CD5−). A significantly greater proportion of CD43+ B cells was found in cord blood and putative HIV + blood samples than in normal control bloods. B‐cell neoplasms derived from each of these four B‐cell subsets were identified, with CD43 +/CD5+ and CD43‐/CD5‐ neoplasms being most common. The predominant B‐cell population coexpressed CD43 alone in 2/39 neoplasms and CD5 alone in four. A minority of cases showed heterogeneous CD43 expression. The B cells in two of three posttransplant lymphoproliferative disorders coexpressed CD43. B cells showed weaker CD43 staining than did T‐cells (relative fluorescence 0.38 ± 0.29).
These findings support the concept that CD43 expression by neoplastic B cells is not an aberrant finding. CD43 expression on normal and neoplastic B cells is independent of CD5 expression even though CD43 and CD5 are frequently coexpressed. CD43 expression by B cells sometimes might be underestimated in paraffin sections because it is much weaker than on T cells. Although large discrete populations of CD43+ B cells were only identified in B‐cell neoplasms and posttransplant lymphoproliferative disorders, increased proportions of CD43+ B cells were present in some benign settings. © 1995 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Ammonium Chloride</subject><subject>Animals</subject><subject>Antibodies - immunology</subject><subject>Antigens, CD</subject><subject>Antigens, CD19 - immunology</subject><subject>B-Lymphocyte Subsets - immunology</subject><subject>B‐cells</subject><subject>CD43</subject><subject>CD5</subject><subject>CD5 Antigens - immunology</subject><subject>Flow Cytometry</subject><subject>HIV</subject><subject>Humans</subject><subject>immunophenotype</subject><subject>Leukosialin</subject><subject>lymphoma</subject><subject>Lymphoma, B-Cell - immunology</subject><subject>posttransplant lymphoproliferative disorder</subject><subject>Reagent Kits, Diagnostic</subject><subject>Sialoglycoproteins - immunology</subject><issn>0196-4763</issn><issn>1097-0320</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUMtOwzAQtBAISuHKDcknbilrO7FrbhCeUiUucOAUxc5GBCV1ayeqeuMT-Ea-hIRW5Yi00kq7M6OZIeSMwYQB8Eu7bt1Ea-AcBIM9MmKgVQSCwz4ZAdMyipUUR-Q4hA8A0DIWh-RwmiRSJ_GILNPbWNB8XtD0Nul3WxlXVBhogWU1R1q6ztO5801e_6Lm6BZ1HtrK0pvvzy-LdU1DZwK24Ype0_bdIw53VztPy9qt6GCwwdb3jNB2xfqEHJR5HfB0u8fk9f7uJX2MZs8PT-n1LLJcJxBxXRgopGEWuRLCChsDK7XmOVNaM8aQqWkiuSpjIzliiYBCyinExiSWGTEmFxvdhXfLDkObNVUY_OZ9hi5kSqmYiX7GZLIBWu9C8FhmC181uV9nDLKh42yIkO067gnnW-XONFjs4NtS-7_e_FdVjet_1LL07eX5T_sHPieKlA</recordid><startdate>19950915</startdate><enddate>19950915</enddate><creator>Lynch, Edward F.</creator><creator>Jones, Patricia A.</creator><creator>Swerdlow, Steven H.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>19950915</creationdate><title>CD43 and CD5 antibodies define four normal and neoplastic B‐cell subsets: A three‐color flow cytometric study</title><author>Lynch, Edward F. ; Jones, Patricia A. ; Swerdlow, Steven H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2950-29db0d6b1ce2733c3c401f992a1799111e1785627f4b62eefe0e366804bb5c1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adult</topic><topic>Ammonium Chloride</topic><topic>Animals</topic><topic>Antibodies - immunology</topic><topic>Antigens, CD</topic><topic>Antigens, CD19 - immunology</topic><topic>B-Lymphocyte Subsets - immunology</topic><topic>B‐cells</topic><topic>CD43</topic><topic>CD5</topic><topic>CD5 Antigens - immunology</topic><topic>Flow Cytometry</topic><topic>HIV</topic><topic>Humans</topic><topic>immunophenotype</topic><topic>Leukosialin</topic><topic>lymphoma</topic><topic>Lymphoma, B-Cell - immunology</topic><topic>posttransplant lymphoproliferative disorder</topic><topic>Reagent Kits, Diagnostic</topic><topic>Sialoglycoproteins - immunology</topic><toplevel>online_resources</toplevel><creatorcontrib>Lynch, Edward F.</creatorcontrib><creatorcontrib>Jones, Patricia A.</creatorcontrib><creatorcontrib>Swerdlow, Steven H.</creatorcontrib><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>Cytometry (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lynch, Edward F.</au><au>Jones, Patricia A.</au><au>Swerdlow, Steven H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD43 and CD5 antibodies define four normal and neoplastic B‐cell subsets: A three‐color flow cytometric study</atitle><jtitle>Cytometry (New York, N.Y.)</jtitle><addtitle>Cytometry</addtitle><date>1995-09-15</date><risdate>1995</risdate><volume>22</volume><issue>3</issue><spage>223</spage><epage>231</epage><pages>223-231</pages><issn>0196-4763</issn><eissn>1097-0320</eissn><abstract>CD43 antibodies are best known for identifying normal and neoplastic T cells and a subset of neoplastic B cells in paraffin sections. The frequency of nonneoplastic CD43 + B cells in different reactive settings, the proportion of B‐cell neoplasms with small CD43+ populations, and the relationship of CD43+ B cells to CD5+ B cells are less well established. CD43 and CD5 expression on normal and neoplastic CD19 + B cells was therefore studied in 138 specimens using three‐color flow cytometric analysis.
CD43 and CD5 defined four normal B‐cell subsets (CD43 + CD5 +, CD43 + CD5−, CD43−CD5+, and CD43−CD5−). A significantly greater proportion of CD43+ B cells was found in cord blood and putative HIV + blood samples than in normal control bloods. B‐cell neoplasms derived from each of these four B‐cell subsets were identified, with CD43 +/CD5+ and CD43‐/CD5‐ neoplasms being most common. The predominant B‐cell population coexpressed CD43 alone in 2/39 neoplasms and CD5 alone in four. A minority of cases showed heterogeneous CD43 expression. The B cells in two of three posttransplant lymphoproliferative disorders coexpressed CD43. B cells showed weaker CD43 staining than did T‐cells (relative fluorescence 0.38 ± 0.29).
These findings support the concept that CD43 expression by neoplastic B cells is not an aberrant finding. CD43 expression on normal and neoplastic B cells is independent of CD5 expression even though CD43 and CD5 are frequently coexpressed. CD43 expression by B cells sometimes might be underestimated in paraffin sections because it is much weaker than on T cells. Although large discrete populations of CD43+ B cells were only identified in B‐cell neoplasms and posttransplant lymphoproliferative disorders, increased proportions of CD43+ B cells were present in some benign settings. © 1995 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8556954</pmid><doi>10.1002/cyto.990220310</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Ammonium Chloride Animals Antibodies - immunology Antigens, CD Antigens, CD19 - immunology B-Lymphocyte Subsets - immunology B‐cells CD43 CD5 CD5 Antigens - immunology Flow Cytometry HIV Humans immunophenotype Leukosialin lymphoma Lymphoma, B-Cell - immunology posttransplant lymphoproliferative disorder Reagent Kits, Diagnostic Sialoglycoproteins - immunology |
title | CD43 and CD5 antibodies define four normal and neoplastic B‐cell subsets: A three‐color flow cytometric study |
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