Autoreactive IgG Memory Antibodies in Patients with Systemic Lupus Erythematosus Arise from Nonreactive and Polyreactive Precursors
Persistent autoantibody production in patients with systemic lupus erythematosus (SLE) suggests the existence of autoreactive humoral memory, but the frequency of self-reactive memory B cells in SLE has not been determined. Here, we report on the reactivity of 200 monoclonal antibodies from single I...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2008-07, Vol.105 (28), p.9727-9732 |
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creator | Mietzner, Brun Tsuiji, Makoto Scheid, Johannes Velinzon, Klara Tiller, Thomas Abraham, Klaus Gonzalez, Jose B. Pascual, Virginia Stichweh, Dorothee Wardemann, Hedda Nussenzweig, Michel C. |
description | Persistent autoantibody production in patients with systemic lupus erythematosus (SLE) suggests the existence of autoreactive humoral memory, but the frequency of self-reactive memory B cells in SLE has not been determined. Here, we report on the reactivity of 200 monoclonal antibodies from single IgG+ memory B cells of four SLE patients. The overall frequency of polyreactive and HEp-2 self-reactive antibodies in this compartment was similar to controls. We found 15% of IgG memory B cell antibodies highly reactive and specific for SLE-associated extractable nuclear antigens (ENA) Ro52 and La in one patient with serum autoantibody titers of the same specificity but not in the other three patients or healthy individuals. The germ-line forms of the ENA antibodies were non-self-reactive or polyreactive with low binding to Ro52, supporting the idea that somatic mutations contributed to autoantibody specificity and reactivity. Heterogeneity in the frequency of memory B cells expressing SLE-associated autoantibodies suggests that this variable may be important in the outcome of therapies that ablate this compartment. |
doi_str_mv | 10.1073/pnas.0803644105 |
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Here, we report on the reactivity of 200 monoclonal antibodies from single IgG+ memory B cells of four SLE patients. The overall frequency of polyreactive and HEp-2 self-reactive antibodies in this compartment was similar to controls. We found 15% of IgG memory B cell antibodies highly reactive and specific for SLE-associated extractable nuclear antigens (ENA) Ro52 and La in one patient with serum autoantibody titers of the same specificity but not in the other three patients or healthy individuals. The germ-line forms of the ENA antibodies were non-self-reactive or polyreactive with low binding to Ro52, supporting the idea that somatic mutations contributed to autoantibody specificity and reactivity. Heterogeneity in the frequency of memory B cells expressing SLE-associated autoantibodies suggests that this variable may be important in the outcome of therapies that ablate this compartment.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0803644105</identifier><identifier>PMID: 18621685</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Antibodies ; Antibody Specificity ; Antigens ; Antigens, Nuclear ; Autoantibodies ; Autoantibodies - immunology ; Autoantigens - immunology ; B lymphocytes ; B-Lymphocytes - immunology ; Biological Sciences ; Cells ; Enzyme linked immunosorbent assay ; Humans ; Immunoglobulin G ; Immunoglobulins ; Immunologic Memory ; Lupus ; Lupus Erythematosus, Systemic - immunology ; Memory ; Monoclonal antibodies ; Mutation ; Plasma cells ; Reactivity ; Receptors ; Ribonucleoproteins - immunology ; SS-B Antigen ; Systemic lupus erythematosus</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (28), p.9727-9732</ispartof><rights>Copyright 2008 The National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jul 15, 2008</rights><rights>2008 by The National Academy of Sciences of the USA</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-95c4ce5452fde2590d934c1f0615e15c6f5610665772a917c52d9b5033cf43893</citedby><cites>FETCH-LOGICAL-c528t-95c4ce5452fde2590d934c1f0615e15c6f5610665772a917c52d9b5033cf43893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/105/28.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25463041$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25463041$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18621685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mietzner, Brun</creatorcontrib><creatorcontrib>Tsuiji, Makoto</creatorcontrib><creatorcontrib>Scheid, Johannes</creatorcontrib><creatorcontrib>Velinzon, Klara</creatorcontrib><creatorcontrib>Tiller, Thomas</creatorcontrib><creatorcontrib>Abraham, Klaus</creatorcontrib><creatorcontrib>Gonzalez, Jose B.</creatorcontrib><creatorcontrib>Pascual, Virginia</creatorcontrib><creatorcontrib>Stichweh, Dorothee</creatorcontrib><creatorcontrib>Wardemann, Hedda</creatorcontrib><creatorcontrib>Nussenzweig, Michel C.</creatorcontrib><title>Autoreactive IgG Memory Antibodies in Patients with Systemic Lupus Erythematosus Arise from Nonreactive and Polyreactive Precursors</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Persistent autoantibody production in patients with systemic lupus erythematosus (SLE) suggests the existence of autoreactive humoral memory, but the frequency of self-reactive memory B cells in SLE has not been determined. Here, we report on the reactivity of 200 monoclonal antibodies from single IgG+ memory B cells of four SLE patients. The overall frequency of polyreactive and HEp-2 self-reactive antibodies in this compartment was similar to controls. We found 15% of IgG memory B cell antibodies highly reactive and specific for SLE-associated extractable nuclear antigens (ENA) Ro52 and La in one patient with serum autoantibody titers of the same specificity but not in the other three patients or healthy individuals. The germ-line forms of the ENA antibodies were non-self-reactive or polyreactive with low binding to Ro52, supporting the idea that somatic mutations contributed to autoantibody specificity and reactivity. Heterogeneity in the frequency of memory B cells expressing SLE-associated autoantibodies suggests that this variable may be important in the outcome of therapies that ablate this compartment.</description><subject>Antibodies</subject><subject>Antibody Specificity</subject><subject>Antigens</subject><subject>Antigens, Nuclear</subject><subject>Autoantibodies</subject><subject>Autoantibodies - immunology</subject><subject>Autoantigens - immunology</subject><subject>B lymphocytes</subject><subject>B-Lymphocytes - immunology</subject><subject>Biological Sciences</subject><subject>Cells</subject><subject>Enzyme linked immunosorbent assay</subject><subject>Humans</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulins</subject><subject>Immunologic Memory</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Memory</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Plasma cells</subject><subject>Reactivity</subject><subject>Receptors</subject><subject>Ribonucleoproteins - immunology</subject><subject>SS-B Antigen</subject><subject>Systemic lupus erythematosus</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1vEzEQxVcIREvhzAmwOCAuacefa1-QoqqUSgEiAWfL8XobR7vr1PYWcuYfx1GiBDjAybL9e29m7FdVzzGcY6jpxXow6RwkUMEYBv6gOsWg8EQwBQ-rUwBSTyQj7KR6ktIKABSX8Lg6wVIQLCQ_rX5OxxyiMzb7e4dubq_RR9eHuEHTIftFaLxLyA9obrJ3Q07ou89L9GWTsuu9RbNxPSZ0FTd56XqTQyq7afTJoTaGHn0Kw8HaDA2ah25zOJhHZ8eYQkxPq0et6ZJ7tl_Pqm_vr75efpjMPl_fXE5nE8uJzBPFLbOOM07axhGuoFGUWdyCwNxhbkXLBQYheF0To3BdVI1acKDUtoxKRc-qdzvf9bjoXWPLQNF0eh19b-JGB-P1nzeDX-rbcK8Jq0tVVgze7A1iuBtdyrr3ybquM4MLY9JCUSxrgv8LEpCyFmLb0uu_wFUY41BeoTCYYs5AFOhiB9kYUoquPbSMQW9joLcx0McYFMXL3yc98vt_L8CrPbBVHu24JlKrmtSFePtvQrdj12X3Ixf0xQ5dpZKlA0s4ExQYpr8A-z_SJA</recordid><startdate>20080715</startdate><enddate>20080715</enddate><creator>Mietzner, Brun</creator><creator>Tsuiji, Makoto</creator><creator>Scheid, Johannes</creator><creator>Velinzon, Klara</creator><creator>Tiller, Thomas</creator><creator>Abraham, Klaus</creator><creator>Gonzalez, Jose B.</creator><creator>Pascual, Virginia</creator><creator>Stichweh, Dorothee</creator><creator>Wardemann, Hedda</creator><creator>Nussenzweig, Michel C.</creator><general>National Academy of Sciences</general><general>National Acad Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080715</creationdate><title>Autoreactive IgG Memory Antibodies in Patients with Systemic Lupus Erythematosus Arise from Nonreactive and Polyreactive Precursors</title><author>Mietzner, Brun ; 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Here, we report on the reactivity of 200 monoclonal antibodies from single IgG+ memory B cells of four SLE patients. The overall frequency of polyreactive and HEp-2 self-reactive antibodies in this compartment was similar to controls. We found 15% of IgG memory B cell antibodies highly reactive and specific for SLE-associated extractable nuclear antigens (ENA) Ro52 and La in one patient with serum autoantibody titers of the same specificity but not in the other three patients or healthy individuals. The germ-line forms of the ENA antibodies were non-self-reactive or polyreactive with low binding to Ro52, supporting the idea that somatic mutations contributed to autoantibody specificity and reactivity. Heterogeneity in the frequency of memory B cells expressing SLE-associated autoantibodies suggests that this variable may be important in the outcome of therapies that ablate this compartment.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>18621685</pmid><doi>10.1073/pnas.0803644105</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Antibody Specificity Antigens Antigens, Nuclear Autoantibodies Autoantibodies - immunology Autoantigens - immunology B lymphocytes B-Lymphocytes - immunology Biological Sciences Cells Enzyme linked immunosorbent assay Humans Immunoglobulin G Immunoglobulins Immunologic Memory Lupus Lupus Erythematosus, Systemic - immunology Memory Monoclonal antibodies Mutation Plasma cells Reactivity Receptors Ribonucleoproteins - immunology SS-B Antigen Systemic lupus erythematosus |
title | Autoreactive IgG Memory Antibodies in Patients with Systemic Lupus Erythematosus Arise from Nonreactive and Polyreactive Precursors |
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