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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
Main Authors: 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
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container_issue 11
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container_title Arthritis & rheumatology (Hoboken, N.J.)
container_volume 68
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
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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 &amp; 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 &amp; 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. 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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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