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Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases
Objective To investigate the potential role of circulating autoantibodies specific to neuronal cell surface antigens in the pathophysiology of neuropsychiatric disorders. Methods Two different kinds of immunoscreening approaches were used to identify autoantigens associated with neuropsychiatric dis...
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Published in: | Arthritis & rheumatology (Hoboken, N.J.) N.J.), 2016-11, Vol.68 (11), p.2708-2716 |
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creator | Delunardo, Federica Soldati, Denise Bellisario, Veronica Berry, Alessandra Camerini, Serena Crescenzi, Marco Alessandri, Cristiano Conti, Fabrizio Ceccarelli, Fulvia Francia, Ada Valesini, Guido Cirulli, Francesca Siracusano, Alberto Siracusano, Alessandra Niolu, Cinzia Alex Rubino, Ivo Ortona, Elena Margutti, Paola |
description | Objective
To investigate the potential role of circulating autoantibodies specific to neuronal cell surface antigens in the pathophysiology of neuropsychiatric disorders.
Methods
Two different kinds of immunoscreening approaches were used to identify autoantigens associated with neuropsychiatric disorders in the serum of patients with schizophrenia. The presence of autoantibodies specific to the identified autoantigens was then tested in patients with various psychiatric disorders and in patients with systemic lupus erythematosus (SLE) and concomitant neuropsychiatric manifestations. Furthermore, the potential pathogenic role of these autoantibodies was assessed both in vitro and in vivo.
Results
GAPDH was identified as a novel autoantigen associated with neuropsychiatric disorders. Serum anti‐GAPDH IgG was detected in the serum of 51% of patients with schizophrenia and 50% of patients with major depression. Moreover, SLE patients with comorbid psychiatric manifestations presented significantly higher serum levels of anti‐GAPDH antibodies than did SLE patients without psychiatric manifestations (P = 0.004 by chi‐square test). Of note, a significant positive correlation (R = 0.48, P = 0.0049, by Spearman's rank correlation test) was found between the levels of serum anti‐GAPDH antibodies and cognitive dysfunction in patients with SLE. In vitro analysis of the effects of purified human anti‐GAPDH autoantibodies on SH‐SY5Y cells showed an immediate neurite retraction. Finally, in vivo administration of anti‐GAPDH autoantibodies in the right cerebral ventricle of C57BL/6J mice resulted in specific behavioral changes associated with a detrimental cognitive and emotional profile.
Conclusion
Overall, these data suggest that anti‐GAPDH autoantibodies play a role in the pathogenesis of neuropsychiatric disorders, thus representing a potentially promising tool for the screening of individual vulnerability to these disabling conditions. |
doi_str_mv | 10.1002/art.39750 |
format | article |
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To investigate the potential role of circulating autoantibodies specific to neuronal cell surface antigens in the pathophysiology of neuropsychiatric disorders.
Methods
Two different kinds of immunoscreening approaches were used to identify autoantigens associated with neuropsychiatric disorders in the serum of patients with schizophrenia. The presence of autoantibodies specific to the identified autoantigens was then tested in patients with various psychiatric disorders and in patients with systemic lupus erythematosus (SLE) and concomitant neuropsychiatric manifestations. Furthermore, the potential pathogenic role of these autoantibodies was assessed both in vitro and in vivo.
Results
GAPDH was identified as a novel autoantigen associated with neuropsychiatric disorders. Serum anti‐GAPDH IgG was detected in the serum of 51% of patients with schizophrenia and 50% of patients with major depression. Moreover, SLE patients with comorbid psychiatric manifestations presented significantly higher serum levels of anti‐GAPDH antibodies than did SLE patients without psychiatric manifestations (P = 0.004 by chi‐square test). Of note, a significant positive correlation (R = 0.48, P = 0.0049, by Spearman's rank correlation test) was found between the levels of serum anti‐GAPDH antibodies and cognitive dysfunction in patients with SLE. In vitro analysis of the effects of purified human anti‐GAPDH autoantibodies on SH‐SY5Y cells showed an immediate neurite retraction. Finally, in vivo administration of anti‐GAPDH autoantibodies in the right cerebral ventricle of C57BL/6J mice resulted in specific behavioral changes associated with a detrimental cognitive and emotional profile.
Conclusion
Overall, these data suggest that anti‐GAPDH autoantibodies play a role in the pathogenesis of neuropsychiatric disorders, thus representing a potentially promising tool for the screening of individual vulnerability to these disabling conditions.</description><identifier>ISSN: 2326-5191</identifier><identifier>EISSN: 2326-5205</identifier><identifier>DOI: 10.1002/art.39750</identifier><identifier>PMID: 27213890</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adult ; Animals ; Autoantibodies - immunology ; Autoantibodies - pharmacology ; Autoantigens ; Behavior, Animal - drug effects ; Biomarkers ; Bipolar Disorder - immunology ; Cell Line, Tumor ; Cognition - drug effects ; Cognitive Dysfunction - immunology ; Depressive Disorder, Major - immunology ; Emotions - drug effects ; Female ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - immunology ; Humans ; Immunoglobulin G - immunology ; Injections, Intraventricular ; Lupus Erythematosus, Systemic - immunology ; Lupus Vasculitis, Central Nervous System - immunology ; Male ; Mice, Inbred C57BL ; Middle Aged ; Neurites - drug effects ; Schizophrenia ; Schizophrenia - immunology ; Young Adult</subject><ispartof>Arthritis & rheumatology (Hoboken, N.J.), 2016-11, Vol.68 (11), p.2708-2716</ispartof><rights>2016, American College of Rheumatology</rights><rights>2016, American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4520-1dfda5a755ca0c1505f4eac706afc232b78b8d800865a6e9c07ae3e74ce55913</citedby><cites>FETCH-LOGICAL-c4520-1dfda5a755ca0c1505f4eac706afc232b78b8d800865a6e9c07ae3e74ce55913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27213890$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Delunardo, Federica</creatorcontrib><creatorcontrib>Soldati, Denise</creatorcontrib><creatorcontrib>Bellisario, Veronica</creatorcontrib><creatorcontrib>Berry, Alessandra</creatorcontrib><creatorcontrib>Camerini, Serena</creatorcontrib><creatorcontrib>Crescenzi, Marco</creatorcontrib><creatorcontrib>Alessandri, Cristiano</creatorcontrib><creatorcontrib>Conti, Fabrizio</creatorcontrib><creatorcontrib>Ceccarelli, Fulvia</creatorcontrib><creatorcontrib>Francia, Ada</creatorcontrib><creatorcontrib>Valesini, Guido</creatorcontrib><creatorcontrib>Cirulli, Francesca</creatorcontrib><creatorcontrib>Siracusano, Alberto</creatorcontrib><creatorcontrib>Siracusano, Alessandra</creatorcontrib><creatorcontrib>Niolu, Cinzia</creatorcontrib><creatorcontrib>Alex Rubino, Ivo</creatorcontrib><creatorcontrib>Ortona, Elena</creatorcontrib><creatorcontrib>Margutti, Paola</creatorcontrib><title>Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases</title><title>Arthritis & rheumatology (Hoboken, N.J.)</title><addtitle>Arthritis Rheumatol</addtitle><description>Objective
To investigate the potential role of circulating autoantibodies specific to neuronal cell surface antigens in the pathophysiology of neuropsychiatric disorders.
Methods
Two different kinds of immunoscreening approaches were used to identify autoantigens associated with neuropsychiatric disorders in the serum of patients with schizophrenia. The presence of autoantibodies specific to the identified autoantigens was then tested in patients with various psychiatric disorders and in patients with systemic lupus erythematosus (SLE) and concomitant neuropsychiatric manifestations. Furthermore, the potential pathogenic role of these autoantibodies was assessed both in vitro and in vivo.
Results
GAPDH was identified as a novel autoantigen associated with neuropsychiatric disorders. Serum anti‐GAPDH IgG was detected in the serum of 51% of patients with schizophrenia and 50% of patients with major depression. Moreover, SLE patients with comorbid psychiatric manifestations presented significantly higher serum levels of anti‐GAPDH antibodies than did SLE patients without psychiatric manifestations (P = 0.004 by chi‐square test). Of note, a significant positive correlation (R = 0.48, P = 0.0049, by Spearman's rank correlation test) was found between the levels of serum anti‐GAPDH antibodies and cognitive dysfunction in patients with SLE. In vitro analysis of the effects of purified human anti‐GAPDH autoantibodies on SH‐SY5Y cells showed an immediate neurite retraction. Finally, in vivo administration of anti‐GAPDH autoantibodies in the right cerebral ventricle of C57BL/6J mice resulted in specific behavioral changes associated with a detrimental cognitive and emotional profile.
Conclusion
Overall, these data suggest that anti‐GAPDH autoantibodies play a role in the pathogenesis of neuropsychiatric disorders, thus representing a potentially promising tool for the screening of individual vulnerability to these disabling conditions.</description><subject>Adult</subject><subject>Animals</subject><subject>Autoantibodies - immunology</subject><subject>Autoantibodies - pharmacology</subject><subject>Autoantigens</subject><subject>Behavior, Animal - drug effects</subject><subject>Biomarkers</subject><subject>Bipolar Disorder - immunology</subject><subject>Cell Line, Tumor</subject><subject>Cognition - drug effects</subject><subject>Cognitive Dysfunction - immunology</subject><subject>Depressive Disorder, Major - immunology</subject><subject>Emotions - drug effects</subject><subject>Female</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - immunology</subject><subject>Humans</subject><subject>Immunoglobulin G - immunology</subject><subject>Injections, Intraventricular</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Vasculitis, Central Nervous System - immunology</subject><subject>Male</subject><subject>Mice, Inbred C57BL</subject><subject>Middle Aged</subject><subject>Neurites - drug effects</subject><subject>Schizophrenia</subject><subject>Schizophrenia - immunology</subject><subject>Young Adult</subject><issn>2326-5191</issn><issn>2326-5205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkctKxDAUhoMoKurCF5CAG12M5tI07bKOVxAdZPblTHqq0U4zJi0yOx_BZ_RJzDjqQhAMgRzCl49z8hOyy9kRZ0wcg--OZK4VWyGbQop0oARTq981z_kG2QnhkcWVa5YytU42hBZcZjnbJE3Rdvb99e2iGJ1e0qLvHMSLiassBgpx0xF0D-4eW2voKXbop7aNCIW2oiPXYaShoSfWTcE_oaeupjfYezcLc_NgofOLdzYgBAzbZK2GJuDO17lFxudn4-Hl4Pr24mpYXA9MEpsf8KquQIFWygAzXDFVJwgmNg-1iWNNdDbJqoyxLFWQYm6YBpSoE4NK5VxukYOldubdc4-hK6c2GGwaaNH1oeSZ1DKRSSb-gYo0zUSik4ju_0IfXe_bOMdCKJLolAvqcEkZ70LwWJczb-PXzEvOykVeZcyr_Mwrsntfxn4yxeqH_E4nAsdL4MU2OP_bVBZ346XyA2lFnyw</recordid><startdate>201611</startdate><enddate>201611</enddate><creator>Delunardo, Federica</creator><creator>Soldati, Denise</creator><creator>Bellisario, Veronica</creator><creator>Berry, Alessandra</creator><creator>Camerini, Serena</creator><creator>Crescenzi, Marco</creator><creator>Alessandri, Cristiano</creator><creator>Conti, Fabrizio</creator><creator>Ceccarelli, Fulvia</creator><creator>Francia, Ada</creator><creator>Valesini, Guido</creator><creator>Cirulli, Francesca</creator><creator>Siracusano, Alberto</creator><creator>Siracusano, Alessandra</creator><creator>Niolu, Cinzia</creator><creator>Alex Rubino, Ivo</creator><creator>Ortona, Elena</creator><creator>Margutti, Paola</creator><general>Wiley Subscription Services, Inc</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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201611</creationdate><title>Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases</title><author>Delunardo, Federica ; Soldati, Denise ; Bellisario, Veronica ; Berry, Alessandra ; Camerini, Serena ; Crescenzi, Marco ; Alessandri, Cristiano ; Conti, Fabrizio ; Ceccarelli, Fulvia ; Francia, Ada ; Valesini, Guido ; Cirulli, Francesca ; Siracusano, Alberto ; Siracusano, Alessandra ; Niolu, Cinzia ; Alex Rubino, Ivo ; Ortona, Elena ; Margutti, Paola</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4520-1dfda5a755ca0c1505f4eac706afc232b78b8d800865a6e9c07ae3e74ce55913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Autoantibodies - immunology</topic><topic>Autoantibodies - pharmacology</topic><topic>Autoantigens</topic><topic>Behavior, Animal - drug effects</topic><topic>Biomarkers</topic><topic>Bipolar Disorder - immunology</topic><topic>Cell Line, Tumor</topic><topic>Cognition - drug effects</topic><topic>Cognitive Dysfunction - immunology</topic><topic>Depressive Disorder, Major - immunology</topic><topic>Emotions - drug effects</topic><topic>Female</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - immunology</topic><topic>Humans</topic><topic>Immunoglobulin G - immunology</topic><topic>Injections, Intraventricular</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Vasculitis, Central Nervous System - immunology</topic><topic>Male</topic><topic>Mice, Inbred C57BL</topic><topic>Middle Aged</topic><topic>Neurites - drug effects</topic><topic>Schizophrenia</topic><topic>Schizophrenia - immunology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delunardo, Federica</creatorcontrib><creatorcontrib>Soldati, Denise</creatorcontrib><creatorcontrib>Bellisario, Veronica</creatorcontrib><creatorcontrib>Berry, Alessandra</creatorcontrib><creatorcontrib>Camerini, Serena</creatorcontrib><creatorcontrib>Crescenzi, Marco</creatorcontrib><creatorcontrib>Alessandri, Cristiano</creatorcontrib><creatorcontrib>Conti, Fabrizio</creatorcontrib><creatorcontrib>Ceccarelli, Fulvia</creatorcontrib><creatorcontrib>Francia, Ada</creatorcontrib><creatorcontrib>Valesini, Guido</creatorcontrib><creatorcontrib>Cirulli, Francesca</creatorcontrib><creatorcontrib>Siracusano, Alberto</creatorcontrib><creatorcontrib>Siracusano, Alessandra</creatorcontrib><creatorcontrib>Niolu, Cinzia</creatorcontrib><creatorcontrib>Alex Rubino, Ivo</creatorcontrib><creatorcontrib>Ortona, Elena</creatorcontrib><creatorcontrib>Margutti, Paola</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delunardo, Federica</au><au>Soldati, Denise</au><au>Bellisario, Veronica</au><au>Berry, Alessandra</au><au>Camerini, Serena</au><au>Crescenzi, Marco</au><au>Alessandri, Cristiano</au><au>Conti, Fabrizio</au><au>Ceccarelli, Fulvia</au><au>Francia, Ada</au><au>Valesini, Guido</au><au>Cirulli, Francesca</au><au>Siracusano, Alberto</au><au>Siracusano, Alessandra</au><au>Niolu, Cinzia</au><au>Alex Rubino, Ivo</au><au>Ortona, Elena</au><au>Margutti, Paola</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases</atitle><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle><addtitle>Arthritis Rheumatol</addtitle><date>2016-11</date><risdate>2016</risdate><volume>68</volume><issue>11</issue><spage>2708</spage><epage>2716</epage><pages>2708-2716</pages><issn>2326-5191</issn><eissn>2326-5205</eissn><abstract>Objective
To investigate the potential role of circulating autoantibodies specific to neuronal cell surface antigens in the pathophysiology of neuropsychiatric disorders.
Methods
Two different kinds of immunoscreening approaches were used to identify autoantigens associated with neuropsychiatric disorders in the serum of patients with schizophrenia. The presence of autoantibodies specific to the identified autoantigens was then tested in patients with various psychiatric disorders and in patients with systemic lupus erythematosus (SLE) and concomitant neuropsychiatric manifestations. Furthermore, the potential pathogenic role of these autoantibodies was assessed both in vitro and in vivo.
Results
GAPDH was identified as a novel autoantigen associated with neuropsychiatric disorders. Serum anti‐GAPDH IgG was detected in the serum of 51% of patients with schizophrenia and 50% of patients with major depression. Moreover, SLE patients with comorbid psychiatric manifestations presented significantly higher serum levels of anti‐GAPDH antibodies than did SLE patients without psychiatric manifestations (P = 0.004 by chi‐square test). Of note, a significant positive correlation (R = 0.48, P = 0.0049, by Spearman's rank correlation test) was found between the levels of serum anti‐GAPDH antibodies and cognitive dysfunction in patients with SLE. In vitro analysis of the effects of purified human anti‐GAPDH autoantibodies on SH‐SY5Y cells showed an immediate neurite retraction. Finally, in vivo administration of anti‐GAPDH autoantibodies in the right cerebral ventricle of C57BL/6J mice resulted in specific behavioral changes associated with a detrimental cognitive and emotional profile.
Conclusion
Overall, these data suggest that anti‐GAPDH autoantibodies play a role in the pathogenesis of neuropsychiatric disorders, thus representing a potentially promising tool for the screening of individual vulnerability to these disabling conditions.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27213890</pmid><doi>10.1002/art.39750</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Animals Autoantibodies - immunology Autoantibodies - pharmacology Autoantigens Behavior, Animal - drug effects Biomarkers Bipolar Disorder - immunology Cell Line, Tumor Cognition - drug effects Cognitive Dysfunction - immunology Depressive Disorder, Major - immunology Emotions - drug effects Female Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) - immunology Humans Immunoglobulin G - immunology Injections, Intraventricular Lupus Erythematosus, Systemic - immunology Lupus Vasculitis, Central Nervous System - immunology Male Mice, Inbred C57BL Middle Aged Neurites - drug effects Schizophrenia Schizophrenia - immunology Young Adult |
title | Anti‐GAPDH Autoantibodies as a Pathogenic Determinant and Potential Biomarker of Neuropsychiatric Diseases |
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