Autoantibodies Targeting Ficolin‐2 in Systemic Lupus Erythematosus Patients With Active Nephritis

Objective Systemic lupus erythematosus (SLE) is a multisystem inflammatory disease characterized by the production of various autoantibodies. The aim of this study was to investigate the presence of anti–ficolin‐2 antibodies in SLE patients and to evaluate the association between the levels of these...

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Veröffentlicht in:Arthritis care & research (2010) 2018-08, Vol.70 (8), p.1263-1268
Hauptverfasser: Colliard, Sophie, Jourde‐Chiche, Noémie, Clavarino, Giovanna, Sarrot‐Reynauld, Françoise, Gout, Evelyne, Deroux, Alban, Fougere, Mélanie, Bardin, Nathalie, Bouillet, Laurence, Cesbron, Jean‐Yves, Thielens, Nicole M., Dumestre‐Pérard, Chantal
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container_end_page 1268
container_issue 8
container_start_page 1263
container_title Arthritis care & research (2010)
container_volume 70
creator Colliard, Sophie
Jourde‐Chiche, Noémie
Clavarino, Giovanna
Sarrot‐Reynauld, Françoise
Gout, Evelyne
Deroux, Alban
Fougere, Mélanie
Bardin, Nathalie
Bouillet, Laurence
Cesbron, Jean‐Yves
Thielens, Nicole M.
Dumestre‐Pérard, Chantal
description Objective Systemic lupus erythematosus (SLE) is a multisystem inflammatory disease characterized by the production of various autoantibodies. The aim of this study was to investigate the presence of anti–ficolin‐2 antibodies in SLE patients and to evaluate the association between the levels of these autoantibodies, clinical manifestations, and disease activity. Methods This is a comparative study using a cohort of 165 SLE patients and 48 healthy subjects. SLE patients were further divided into 2 groups (low disease activity [SLE Disease Activity Index (SLEDAI) score ≤4, n = 88] and high disease activity [SLEDAI score >4, n = 77]). Clinical manifestations were defined according to the physician in charge. Active lupus nephritis (LN) was documented by kidney biopsy. Detection of anti–ficolin‐2 antibodies was performed by enzyme‐linked immunosorbent assay. Results Levels of anti–ficolin‐2 autoantibodies were significantly higher in SLE patients as compared to healthy subjects and associated with SLEDAI score. They were found to be positive in 61 of 165 SLE patients (37%). The presence of anti–ficolin‐2 antibodies was significantly related only to renal involvement, with a very high prevalence (86%) of anti–ficolin‐2 antibodies in SLE patients with active LN. Patients with active proliferative LN had significantly more positive anti–ficolin‐2 antibodies than those with nonproliferative LN. The combination of anti–ficolin‐2, anti–ficolin‐3, and anti‐C1q demonstrated a very high specificity (98%) for the diagnosis of active LN. Conclusion Our results support the usefulness of anti–ficolin‐2 as a complementary serologic biomarker for the diagnosis of active lupus with renal manifestations.
doi_str_mv 10.1002/acr.23449
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The aim of this study was to investigate the presence of anti–ficolin‐2 antibodies in SLE patients and to evaluate the association between the levels of these autoantibodies, clinical manifestations, and disease activity. Methods This is a comparative study using a cohort of 165 SLE patients and 48 healthy subjects. SLE patients were further divided into 2 groups (low disease activity [SLE Disease Activity Index (SLEDAI) score ≤4, n = 88] and high disease activity [SLEDAI score &gt;4, n = 77]). Clinical manifestations were defined according to the physician in charge. Active lupus nephritis (LN) was documented by kidney biopsy. Detection of anti–ficolin‐2 antibodies was performed by enzyme‐linked immunosorbent assay. Results Levels of anti–ficolin‐2 autoantibodies were significantly higher in SLE patients as compared to healthy subjects and associated with SLEDAI score. They were found to be positive in 61 of 165 SLE patients (37%). The presence of anti–ficolin‐2 antibodies was significantly related only to renal involvement, with a very high prevalence (86%) of anti–ficolin‐2 antibodies in SLE patients with active LN. Patients with active proliferative LN had significantly more positive anti–ficolin‐2 antibodies than those with nonproliferative LN. The combination of anti–ficolin‐2, anti–ficolin‐3, and anti‐C1q demonstrated a very high specificity (98%) for the diagnosis of active LN. Conclusion Our results support the usefulness of anti–ficolin‐2 as a complementary serologic biomarker for the diagnosis of active lupus with renal manifestations.</description><identifier>ISSN: 2151-464X</identifier><identifier>ISSN: 0893-7524</identifier><identifier>EISSN: 2151-4658</identifier><identifier>EISSN: 1529-0123</identifier><identifier>DOI: 10.1002/acr.23449</identifier><identifier>PMID: 29045037</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Antibodies, Antinuclear - blood ; Autoantibodies ; Autoantibodies - blood ; Autoantibodies - immunology ; Biomarkers - metabolism ; Biopsy ; Biopsy, Needle ; Diagnosis ; Enzyme-Linked Immunosorbent Assay - methods ; Female ; Ficolins ; Human health and pathology ; Humans ; Immunoglobulins ; Immunohistochemistry ; Immunology ; Lectins - metabolism ; Life Sciences ; Lupus ; Lupus Erythematosus, Systemic - blood ; Lupus Erythematosus, Systemic - diagnosis ; Lupus Erythematosus, Systemic - epidemiology ; Lupus nephritis ; Lupus Nephritis - blood ; Lupus Nephritis - diagnosis ; Lupus Nephritis - epidemiology ; Male ; Middle Aged ; Nephritis ; Prevalence ; Rhumatology and musculoskeletal system ; Sensitivity and Specificity ; Severity of Illness Index ; Systemic lupus erythematosus</subject><ispartof>Arthritis care &amp; research (2010), 2018-08, Vol.70 (8), p.1263-1268</ispartof><rights>2017, American College of Rheumatology</rights><rights>2017, American College of Rheumatology.</rights><rights>2018 American College of Rheumatology</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4229-bbf0e974a3553a601b198b2cb244edcbd4ea77ebf2c7061fd3ed91f5b2204d593</citedby><cites>FETCH-LOGICAL-c4229-bbf0e974a3553a601b198b2cb244edcbd4ea77ebf2c7061fd3ed91f5b2204d593</cites><orcidid>0000-0001-9315-1577 ; 0000-0003-3680-082X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Facr.23449$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Facr.23449$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29045037$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01696101$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Colliard, Sophie</creatorcontrib><creatorcontrib>Jourde‐Chiche, Noémie</creatorcontrib><creatorcontrib>Clavarino, Giovanna</creatorcontrib><creatorcontrib>Sarrot‐Reynauld, Françoise</creatorcontrib><creatorcontrib>Gout, Evelyne</creatorcontrib><creatorcontrib>Deroux, Alban</creatorcontrib><creatorcontrib>Fougere, Mélanie</creatorcontrib><creatorcontrib>Bardin, Nathalie</creatorcontrib><creatorcontrib>Bouillet, Laurence</creatorcontrib><creatorcontrib>Cesbron, Jean‐Yves</creatorcontrib><creatorcontrib>Thielens, Nicole M.</creatorcontrib><creatorcontrib>Dumestre‐Pérard, Chantal</creatorcontrib><title>Autoantibodies Targeting Ficolin‐2 in Systemic Lupus Erythematosus Patients With Active Nephritis</title><title>Arthritis care &amp; research (2010)</title><addtitle>Arthritis Care Res (Hoboken)</addtitle><description>Objective Systemic lupus erythematosus (SLE) is a multisystem inflammatory disease characterized by the production of various autoantibodies. The aim of this study was to investigate the presence of anti–ficolin‐2 antibodies in SLE patients and to evaluate the association between the levels of these autoantibodies, clinical manifestations, and disease activity. Methods This is a comparative study using a cohort of 165 SLE patients and 48 healthy subjects. SLE patients were further divided into 2 groups (low disease activity [SLE Disease Activity Index (SLEDAI) score ≤4, n = 88] and high disease activity [SLEDAI score &gt;4, n = 77]). Clinical manifestations were defined according to the physician in charge. Active lupus nephritis (LN) was documented by kidney biopsy. Detection of anti–ficolin‐2 antibodies was performed by enzyme‐linked immunosorbent assay. Results Levels of anti–ficolin‐2 autoantibodies were significantly higher in SLE patients as compared to healthy subjects and associated with SLEDAI score. They were found to be positive in 61 of 165 SLE patients (37%). The presence of anti–ficolin‐2 antibodies was significantly related only to renal involvement, with a very high prevalence (86%) of anti–ficolin‐2 antibodies in SLE patients with active LN. Patients with active proliferative LN had significantly more positive anti–ficolin‐2 antibodies than those with nonproliferative LN. The combination of anti–ficolin‐2, anti–ficolin‐3, and anti‐C1q demonstrated a very high specificity (98%) for the diagnosis of active LN. Conclusion Our results support the usefulness of anti–ficolin‐2 as a complementary serologic biomarker for the diagnosis of active lupus with renal manifestations.</description><subject>Adult</subject><subject>Antibodies, Antinuclear - blood</subject><subject>Autoantibodies</subject><subject>Autoantibodies - blood</subject><subject>Autoantibodies - immunology</subject><subject>Biomarkers - metabolism</subject><subject>Biopsy</subject><subject>Biopsy, Needle</subject><subject>Diagnosis</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Female</subject><subject>Ficolins</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunohistochemistry</subject><subject>Immunology</subject><subject>Lectins - metabolism</subject><subject>Life Sciences</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - blood</subject><subject>Lupus Erythematosus, Systemic - diagnosis</subject><subject>Lupus Erythematosus, Systemic - epidemiology</subject><subject>Lupus nephritis</subject><subject>Lupus Nephritis - blood</subject><subject>Lupus Nephritis - diagnosis</subject><subject>Lupus Nephritis - epidemiology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nephritis</subject><subject>Prevalence</subject><subject>Rhumatology and musculoskeletal system</subject><subject>Sensitivity and Specificity</subject><subject>Severity of Illness Index</subject><subject>Systemic lupus erythematosus</subject><issn>2151-464X</issn><issn>0893-7524</issn><issn>2151-4658</issn><issn>1529-0123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1O3DAQxy3UChDlwAsgS72Uw4I_k_gYraAgrdqqpWpvlu1MWKMk3toO1d54BJ6RJ2nowiJV6lzmQz_9Z0Z_hI4oOaWEsDPj4injQqgdtM-opDNRyOrNthY_99BhSrdkCs6qiqtdtMcUEZLwch-5eszBDNnb0HhI-NrEG8h-uMEX3oXOD4_3Dwz7AX9bpwy9d3gxrsaEz-M6L6E3OaSp-2KyhyEn_MPnJa5d9neAP8FqGX326R1625ouweFzPkDfL86v55ezxeePV_N6MXOCMTWztiWgSmG4lNwUhFqqKsucZUJA42wjwJQl2Ja5khS0bTg0irbSMkZEIxU_QCcb3aXp9Cr63sS1Dsbry3qhn2aEFqqghN7Rif2wYVcx_BohZd375KDrzABhTJoqySSrVCEn9P0_6G0Y4zB9ohkpC8W5rMrX5S6GlCK02wso0U9G6cko_deoiT1-VhxtD82WfLFlAs42wG_fwfr_Srqef91I_gFP2JzY</recordid><startdate>201808</startdate><enddate>201808</enddate><creator>Colliard, Sophie</creator><creator>Jourde‐Chiche, Noémie</creator><creator>Clavarino, Giovanna</creator><creator>Sarrot‐Reynauld, Françoise</creator><creator>Gout, Evelyne</creator><creator>Deroux, Alban</creator><creator>Fougere, Mélanie</creator><creator>Bardin, Nathalie</creator><creator>Bouillet, Laurence</creator><creator>Cesbron, Jean‐Yves</creator><creator>Thielens, Nicole M.</creator><creator>Dumestre‐Pérard, Chantal</creator><general>Wiley Subscription Services, Inc</general><general>Wiley-Blackwell</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>7QP</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-9315-1577</orcidid><orcidid>https://orcid.org/0000-0003-3680-082X</orcidid></search><sort><creationdate>201808</creationdate><title>Autoantibodies Targeting Ficolin‐2 in Systemic Lupus Erythematosus Patients With Active Nephritis</title><author>Colliard, Sophie ; Jourde‐Chiche, Noémie ; Clavarino, Giovanna ; Sarrot‐Reynauld, Françoise ; Gout, Evelyne ; Deroux, Alban ; Fougere, Mélanie ; Bardin, Nathalie ; Bouillet, Laurence ; Cesbron, Jean‐Yves ; Thielens, Nicole M. ; Dumestre‐Pérard, Chantal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4229-bbf0e974a3553a601b198b2cb244edcbd4ea77ebf2c7061fd3ed91f5b2204d593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Antibodies, Antinuclear - blood</topic><topic>Autoantibodies</topic><topic>Autoantibodies - blood</topic><topic>Autoantibodies - immunology</topic><topic>Biomarkers - metabolism</topic><topic>Biopsy</topic><topic>Biopsy, Needle</topic><topic>Diagnosis</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Female</topic><topic>Ficolins</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Immunohistochemistry</topic><topic>Immunology</topic><topic>Lectins - metabolism</topic><topic>Life Sciences</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - blood</topic><topic>Lupus Erythematosus, Systemic - diagnosis</topic><topic>Lupus Erythematosus, Systemic - epidemiology</topic><topic>Lupus nephritis</topic><topic>Lupus Nephritis - blood</topic><topic>Lupus Nephritis - diagnosis</topic><topic>Lupus Nephritis - epidemiology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nephritis</topic><topic>Prevalence</topic><topic>Rhumatology and musculoskeletal system</topic><topic>Sensitivity and Specificity</topic><topic>Severity of Illness Index</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Colliard, Sophie</creatorcontrib><creatorcontrib>Jourde‐Chiche, Noémie</creatorcontrib><creatorcontrib>Clavarino, Giovanna</creatorcontrib><creatorcontrib>Sarrot‐Reynauld, Françoise</creatorcontrib><creatorcontrib>Gout, Evelyne</creatorcontrib><creatorcontrib>Deroux, Alban</creatorcontrib><creatorcontrib>Fougere, Mélanie</creatorcontrib><creatorcontrib>Bardin, Nathalie</creatorcontrib><creatorcontrib>Bouillet, Laurence</creatorcontrib><creatorcontrib>Cesbron, Jean‐Yves</creatorcontrib><creatorcontrib>Thielens, Nicole M.</creatorcontrib><creatorcontrib>Dumestre‐Pérard, Chantal</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Arthritis care &amp; research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Colliard, Sophie</au><au>Jourde‐Chiche, Noémie</au><au>Clavarino, Giovanna</au><au>Sarrot‐Reynauld, Françoise</au><au>Gout, Evelyne</au><au>Deroux, Alban</au><au>Fougere, Mélanie</au><au>Bardin, Nathalie</au><au>Bouillet, Laurence</au><au>Cesbron, Jean‐Yves</au><au>Thielens, Nicole M.</au><au>Dumestre‐Pérard, Chantal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autoantibodies Targeting Ficolin‐2 in Systemic Lupus Erythematosus Patients With Active Nephritis</atitle><jtitle>Arthritis care &amp; research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2018-08</date><risdate>2018</risdate><volume>70</volume><issue>8</issue><spage>1263</spage><epage>1268</epage><pages>1263-1268</pages><issn>2151-464X</issn><issn>0893-7524</issn><eissn>2151-4658</eissn><eissn>1529-0123</eissn><abstract>Objective Systemic lupus erythematosus (SLE) is a multisystem inflammatory disease characterized by the production of various autoantibodies. The aim of this study was to investigate the presence of anti–ficolin‐2 antibodies in SLE patients and to evaluate the association between the levels of these autoantibodies, clinical manifestations, and disease activity. Methods This is a comparative study using a cohort of 165 SLE patients and 48 healthy subjects. SLE patients were further divided into 2 groups (low disease activity [SLE Disease Activity Index (SLEDAI) score ≤4, n = 88] and high disease activity [SLEDAI score &gt;4, n = 77]). Clinical manifestations were defined according to the physician in charge. Active lupus nephritis (LN) was documented by kidney biopsy. Detection of anti–ficolin‐2 antibodies was performed by enzyme‐linked immunosorbent assay. Results Levels of anti–ficolin‐2 autoantibodies were significantly higher in SLE patients as compared to healthy subjects and associated with SLEDAI score. They were found to be positive in 61 of 165 SLE patients (37%). The presence of anti–ficolin‐2 antibodies was significantly related only to renal involvement, with a very high prevalence (86%) of anti–ficolin‐2 antibodies in SLE patients with active LN. Patients with active proliferative LN had significantly more positive anti–ficolin‐2 antibodies than those with nonproliferative LN. The combination of anti–ficolin‐2, anti–ficolin‐3, and anti‐C1q demonstrated a very high specificity (98%) for the diagnosis of active LN. Conclusion Our results support the usefulness of anti–ficolin‐2 as a complementary serologic biomarker for the diagnosis of active lupus with renal manifestations.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29045037</pmid><doi>10.1002/acr.23449</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-9315-1577</orcidid><orcidid>https://orcid.org/0000-0003-3680-082X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adult
Antibodies, Antinuclear - blood
Autoantibodies
Autoantibodies - blood
Autoantibodies - immunology
Biomarkers - metabolism
Biopsy
Biopsy, Needle
Diagnosis
Enzyme-Linked Immunosorbent Assay - methods
Female
Ficolins
Human health and pathology
Humans
Immunoglobulins
Immunohistochemistry
Immunology
Lectins - metabolism
Life Sciences
Lupus
Lupus Erythematosus, Systemic - blood
Lupus Erythematosus, Systemic - diagnosis
Lupus Erythematosus, Systemic - epidemiology
Lupus nephritis
Lupus Nephritis - blood
Lupus Nephritis - diagnosis
Lupus Nephritis - epidemiology
Male
Middle Aged
Nephritis
Prevalence
Rhumatology and musculoskeletal system
Sensitivity and Specificity
Severity of Illness Index
Systemic lupus erythematosus
title Autoantibodies Targeting Ficolin‐2 in Systemic Lupus Erythematosus Patients With Active Nephritis
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