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Humoral response against small heat shock proteins in Parkinson's disease
In the light of evidence for the increased heat shock proteins (HSP) expression in neurodegenerative disorders, the presence of the adaptive humoral response of the immune system can be expected. The aim of the study was to check whether Parkinson's disease (PD) has the ability to elicit immune...
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Published in: | PloS one 2015-01, Vol.10 (1), p.e0115480-e0115480 |
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description | In the light of evidence for the increased heat shock proteins (HSP) expression in neurodegenerative disorders, the presence of the adaptive humoral response of the immune system can be expected. The aim of the study was to check whether Parkinson's disease (PD) has the ability to elicit immune response against small heat shock proteins.
IgG and IgM autoantibodies against alpha B-crystallin were assessed in 26 PD patients 26 healthy subjects. For the assessment of anti-HSP IgG autoantibodies serum samples from 31 parkinsonian patients and 31 healthy control subjects were collected. Serum samples from PD patients and healthy control subjects were collected twice, at baseline and after mean of 13 months follow up.
Both IgM and IgG autoantibodies against alpha ß-crystallin in PD patients were significantly higher compared to healthy controls (p |
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IgG and IgM autoantibodies against alpha B-crystallin were assessed in 26 PD patients 26 healthy subjects. For the assessment of anti-HSP IgG autoantibodies serum samples from 31 parkinsonian patients and 31 healthy control subjects were collected. Serum samples from PD patients and healthy control subjects were collected twice, at baseline and after mean of 13 months follow up.
Both IgM and IgG autoantibodies against alpha ß-crystallin in PD patients were significantly higher compared to healthy controls (p<0.05). We also found statistically significant increase in antibodies titers against alpha ß-crystallin over the time of 13 months, both for IgG (p = 0.021) and for IgM (p<0.0001). Additionally, PD patients presented higher levels of anti-HSP IgG autoantibodies than healthy controls (p = 0.02).
Increase of IgG and IgM autoantibodies against alpha B-crystallin in PD patients over time may suggest their involvement in the disease pathogenesis and progression. Further studies are required to confirm the role of this antibody as a biomarker of the disease progression.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0115480</identifier><identifier>PMID: 25629316</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adaptive systems ; Aged ; alpha-Crystallin B Chain - immunology ; Antibodies ; Antigens ; Apoptosis ; Atherosclerosis ; Autoantibodies ; Autoantibodies - blood ; Autoantibodies - immunology ; Autoimmunity ; Basal ganglia ; Biomarkers ; Case-Control Studies ; Central nervous system diseases ; Crystal structure ; Crystallin ; Crystallinity ; Dementia ; Female ; Heat shock proteins ; Heat-Shock Proteins, Small - immunology ; Homeostasis ; Humans ; Immune response ; Immune response (humoral) ; Immune system ; Immunity, Humoral ; Immunoglobulin G ; Immunoglobulin G - blood ; Immunoglobulin G - immunology ; Immunoglobulin M ; Immunoglobulin M - blood ; Immunoglobulin M - immunology ; Immunoglobulins ; Male ; Middle Aged ; Movement disorders ; Neurodegenerative diseases ; Neurology ; Parkinson Disease - blood ; Parkinson Disease - immunology ; Parkinson's disease ; Pathogenesis ; Patients ; Proteins ; Small heat shock proteins ; Statistical analysis ; Statistical methods ; Toxicity</subject><ispartof>PloS one, 2015-01, Vol.10 (1), p.e0115480-e0115480</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Papuć et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Papuć et al 2015 Papuć et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-ee9bba2f6500d90cb0b1bdf76ea535ed9f5d9e9c7b5d2a62f8f14c1ebc0eb9963</citedby><cites>FETCH-LOGICAL-c692t-ee9bba2f6500d90cb0b1bdf76ea535ed9f5d9e9c7b5d2a62f8f14c1ebc0eb9963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1650212910/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1650212910?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,315,733,786,790,891,25783,27957,27958,37047,37048,44625,53827,53829,75483</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25629316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Cohen, Irun R</contributor><creatorcontrib>Papuć, Ewa</creatorcontrib><creatorcontrib>Kurys-Denis, Ewa</creatorcontrib><creatorcontrib>Krupski, Witold</creatorcontrib><creatorcontrib>Rejdak, Konrad</creatorcontrib><title>Humoral response against small heat shock proteins in Parkinson's disease</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>In the light of evidence for the increased heat shock proteins (HSP) expression in neurodegenerative disorders, the presence of the adaptive humoral response of the immune system can be expected. The aim of the study was to check whether Parkinson's disease (PD) has the ability to elicit immune response against small heat shock proteins.
IgG and IgM autoantibodies against alpha B-crystallin were assessed in 26 PD patients 26 healthy subjects. For the assessment of anti-HSP IgG autoantibodies serum samples from 31 parkinsonian patients and 31 healthy control subjects were collected. Serum samples from PD patients and healthy control subjects were collected twice, at baseline and after mean of 13 months follow up.
Both IgM and IgG autoantibodies against alpha ß-crystallin in PD patients were significantly higher compared to healthy controls (p<0.05). We also found statistically significant increase in antibodies titers against alpha ß-crystallin over the time of 13 months, both for IgG (p = 0.021) and for IgM (p<0.0001). Additionally, PD patients presented higher levels of anti-HSP IgG autoantibodies than healthy controls (p = 0.02).
Increase of IgG and IgM autoantibodies against alpha B-crystallin in PD patients over time may suggest their involvement in the disease pathogenesis and progression. Further studies are required to confirm the role of this antibody as a biomarker of the disease progression.</description><subject>Adaptive systems</subject><subject>Aged</subject><subject>alpha-Crystallin B Chain - immunology</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Apoptosis</subject><subject>Atherosclerosis</subject><subject>Autoantibodies</subject><subject>Autoantibodies - blood</subject><subject>Autoantibodies - immunology</subject><subject>Autoimmunity</subject><subject>Basal ganglia</subject><subject>Biomarkers</subject><subject>Case-Control Studies</subject><subject>Central nervous system diseases</subject><subject>Crystal structure</subject><subject>Crystallin</subject><subject>Crystallinity</subject><subject>Dementia</subject><subject>Female</subject><subject>Heat shock proteins</subject><subject>Heat-Shock Proteins, Small - immunology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune response (humoral)</subject><subject>Immune system</subject><subject>Immunity, Humoral</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin G - immunology</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulin M - blood</subject><subject>Immunoglobulin M - immunology</subject><subject>Immunoglobulins</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Movement disorders</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Parkinson Disease - blood</subject><subject>Parkinson Disease - immunology</subject><subject>Parkinson's disease</subject><subject>Pathogenesis</subject><subject>Patients</subject><subject>Proteins</subject><subject>Small heat shock proteins</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Toxicity</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkktv1DAUhSMEoqXwDxBEQuKxmMGP2Ik3SFUFdKRKRby2lmNfZzxN4qmdIPj3eDppNUFdoCx8ZX_32PfkZNlzjJaYlvj9xo-hV-1y63tYIoxZUaEH2TEWlCw4QfThQX2UPYlxgxCjFeePsyPCOBEU8-NsdT52Pqg2DxCTUoRcNcr1cchjp9o2X4NK5drrq3wb_ADpKHd9_kWFq1T6_k3MjYugIjzNHlnVRng2rSfZj08fv5-dLy4uP6_OTi8WmgsyLABEXStiOUPICKRrVOPa2JKDYpSBEZYZAUKXNTNEcWIriwuNodYIaiE4Pcle7nW3rY9yciFKnAQJJgKjRKz2hPFqI7fBdSr8kV45ebPhQyNVGJxuQWqDERPWmlLQQmlT1Th5VJXprUwVpEpaH6bbxroDo6Efklsz0flJ79ay8b9kQZFIAyWBt5NA8NcjxEF2LmpoW9WDH2_eTQrCCiES-uof9P7pJqpRaQDXW5_u1TtReVoQxFFJ6Y5a3kOlz0DndIqMdWl_1vBu1pCYAX4PjRpjlKtvX_-fvfw5Z18fsClO7bCOvh0Hl9I2B4s9qIOPMYC9MxkjuUv8rRtyl3g5JT61vTj8QXdNtxGnfwHZfvt-</recordid><startdate>20150128</startdate><enddate>20150128</enddate><creator>Papuć, Ewa</creator><creator>Kurys-Denis, Ewa</creator><creator>Krupski, Witold</creator><creator>Rejdak, Konrad</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150128</creationdate><title>Humoral response against small heat shock proteins in Parkinson's disease</title><author>Papuć, Ewa ; Kurys-Denis, Ewa ; Krupski, Witold ; Rejdak, Konrad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-ee9bba2f6500d90cb0b1bdf76ea535ed9f5d9e9c7b5d2a62f8f14c1ebc0eb9963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adaptive systems</topic><topic>Aged</topic><topic>alpha-Crystallin B Chain - 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blood</topic><topic>Parkinson Disease - immunology</topic><topic>Parkinson's disease</topic><topic>Pathogenesis</topic><topic>Patients</topic><topic>Proteins</topic><topic>Small heat shock proteins</topic><topic>Statistical analysis</topic><topic>Statistical methods</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Papuć, Ewa</creatorcontrib><creatorcontrib>Kurys-Denis, Ewa</creatorcontrib><creatorcontrib>Krupski, Witold</creatorcontrib><creatorcontrib>Rejdak, Konrad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Papuć, Ewa</au><au>Kurys-Denis, Ewa</au><au>Krupski, Witold</au><au>Rejdak, Konrad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Humoral response against small heat shock proteins in Parkinson's disease</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-01-28</date><risdate>2015</risdate><volume>10</volume><issue>1</issue><spage>e0115480</spage><epage>e0115480</epage><pages>e0115480-e0115480</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><notes>ObjectType-Article-1</notes><notes>SourceType-Scholarly Journals-1</notes><notes>ObjectType-Feature-2</notes><notes>content type line 23</notes><notes>Competing Interests: The authors have declared that no competing interests exist.</notes><notes>Conceived and designed the experiments: EP. Performed the experiments: EP EKD. Analyzed the data: EP EKD. Contributed reagents/materials/analysis tools: EP EKD. Wrote the paper: EP. Critique of the manuscript: KR WK.</notes><abstract>In the light of evidence for the increased heat shock proteins (HSP) expression in neurodegenerative disorders, the presence of the adaptive humoral response of the immune system can be expected. The aim of the study was to check whether Parkinson's disease (PD) has the ability to elicit immune response against small heat shock proteins.
IgG and IgM autoantibodies against alpha B-crystallin were assessed in 26 PD patients 26 healthy subjects. For the assessment of anti-HSP IgG autoantibodies serum samples from 31 parkinsonian patients and 31 healthy control subjects were collected. Serum samples from PD patients and healthy control subjects were collected twice, at baseline and after mean of 13 months follow up.
Both IgM and IgG autoantibodies against alpha ß-crystallin in PD patients were significantly higher compared to healthy controls (p<0.05). We also found statistically significant increase in antibodies titers against alpha ß-crystallin over the time of 13 months, both for IgG (p = 0.021) and for IgM (p<0.0001). Additionally, PD patients presented higher levels of anti-HSP IgG autoantibodies than healthy controls (p = 0.02).
Increase of IgG and IgM autoantibodies against alpha B-crystallin in PD patients over time may suggest their involvement in the disease pathogenesis and progression. Further studies are required to confirm the role of this antibody as a biomarker of the disease progression.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25629316</pmid><doi>10.1371/journal.pone.0115480</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adaptive systems Aged alpha-Crystallin B Chain - immunology Antibodies Antigens Apoptosis Atherosclerosis Autoantibodies Autoantibodies - blood Autoantibodies - immunology Autoimmunity Basal ganglia Biomarkers Case-Control Studies Central nervous system diseases Crystal structure Crystallin Crystallinity Dementia Female Heat shock proteins Heat-Shock Proteins, Small - immunology Homeostasis Humans Immune response Immune response (humoral) Immune system Immunity, Humoral Immunoglobulin G Immunoglobulin G - blood Immunoglobulin G - immunology Immunoglobulin M Immunoglobulin M - blood Immunoglobulin M - immunology Immunoglobulins Male Middle Aged Movement disorders Neurodegenerative diseases Neurology Parkinson Disease - blood Parkinson Disease - immunology Parkinson's disease Pathogenesis Patients Proteins Small heat shock proteins Statistical analysis Statistical methods Toxicity |
title | Humoral response against small heat shock proteins in Parkinson's disease |
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