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Complement Split Products C3a and C4a in Chronic Lyme Disease
Complement split products C3a and C4a are reportedly elevated in patients with acute Lyme disease. We have now examined these immunologic markers in patients with chronic Lyme disease compared to appropriate disease controls. The study population consisted of 29 healthy controls, 445 patients with c...
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Published in: | Scandinavian journal of immunology 2009, Vol.69 (1), p.64-69 |
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description | Complement split products C3a and C4a are reportedly elevated in patients with acute Lyme disease. We have now examined these immunologic markers in patients with chronic Lyme disease compared to appropriate disease controls. The study population consisted of 29 healthy controls, 445 patients with chronic Lyme disease, 11 patients with systemic lupus erythematosus (SLE) and six patients with AIDS. The Lyme disease patients were divided according to predominant musculoskeletal symptoms (324 patients) or predominant neurologic symptoms (121 patients). C3a and C4a levels were measured by radioimmunoassay. All patients with chronic Lyme disease and AIDS had normal C3a levels compared to controls, whereas patients with SLE had significantly increased levels of this marker. Patients with predominant musculoskeletal symptoms of Lyme disease and AIDS patients had significantly increased levels of C4a compared to either controls, patients with predominant neurologic symptoms of Lyme disease or SLE patients. Response to antibiotic therapy in chronic Lyme disease was associated with a significant decrease in the C4a level, whereas lack of response was associated with a significant increase in this marker. In contrast, AIDS patients had persistently increased C4a levels despite antiretroviral therapy. Lyme patients with positive single-photon emission computed tomographic (SPECT) scans had significantly lower C4a levels compared to Lyme patients with normal SPECT scan results. Patients with predominant musculoskeletal symptoms of Lyme disease have normal C3a and increased C4a levels. This pattern differs from the increase in both markers seen in acute Lyme disease, and C4a changes correlate with the response to therapy in chronic Lyme disease. C4a appears to be a valuable immunologic marker in patients with persistent symptoms of Lyme disease. |
doi_str_mv | 10.1111/j.1365-3083.2008.02191.x |
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We have now examined these immunologic markers in patients with chronic Lyme disease compared to appropriate disease controls. The study population consisted of 29 healthy controls, 445 patients with chronic Lyme disease, 11 patients with systemic lupus erythematosus (SLE) and six patients with AIDS. The Lyme disease patients were divided according to predominant musculoskeletal symptoms (324 patients) or predominant neurologic symptoms (121 patients). C3a and C4a levels were measured by radioimmunoassay. All patients with chronic Lyme disease and AIDS had normal C3a levels compared to controls, whereas patients with SLE had significantly increased levels of this marker. Patients with predominant musculoskeletal symptoms of Lyme disease and AIDS patients had significantly increased levels of C4a compared to either controls, patients with predominant neurologic symptoms of Lyme disease or SLE patients. Response to antibiotic therapy in chronic Lyme disease was associated with a significant decrease in the C4a level, whereas lack of response was associated with a significant increase in this marker. In contrast, AIDS patients had persistently increased C4a levels despite antiretroviral therapy. Lyme patients with positive single-photon emission computed tomographic (SPECT) scans had significantly lower C4a levels compared to Lyme patients with normal SPECT scan results. Patients with predominant musculoskeletal symptoms of Lyme disease have normal C3a and increased C4a levels. This pattern differs from the increase in both markers seen in acute Lyme disease, and C4a changes correlate with the response to therapy in chronic Lyme disease. C4a appears to be a valuable immunologic marker in patients with persistent symptoms of Lyme disease.</description><identifier>ISSN: 0300-9475</identifier><identifier>EISSN: 1365-3083</identifier><identifier>DOI: 10.1111/j.1365-3083.2008.02191.x</identifier><identifier>PMID: 19140878</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anti-Infective Agents - therapeutic use ; Biomarkers - analysis ; Borrelia ; Child ; Chronic Disease ; Complement C3a - analysis ; Complement C3a - immunology ; Complement C4a - analysis ; Complement C4a - immunology ; Female ; Humans ; Lyme Disease - drug therapy ; Lyme Disease - immunology ; Male ; Middle Aged ; Radioimmunoassay ; Young Adult</subject><ispartof>Scandinavian journal of immunology, 2009, Vol.69 (1), p.64-69</ispartof><rights>2008 The Authors. 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We have now examined these immunologic markers in patients with chronic Lyme disease compared to appropriate disease controls. The study population consisted of 29 healthy controls, 445 patients with chronic Lyme disease, 11 patients with systemic lupus erythematosus (SLE) and six patients with AIDS. The Lyme disease patients were divided according to predominant musculoskeletal symptoms (324 patients) or predominant neurologic symptoms (121 patients). C3a and C4a levels were measured by radioimmunoassay. All patients with chronic Lyme disease and AIDS had normal C3a levels compared to controls, whereas patients with SLE had significantly increased levels of this marker. Patients with predominant musculoskeletal symptoms of Lyme disease and AIDS patients had significantly increased levels of C4a compared to either controls, patients with predominant neurologic symptoms of Lyme disease or SLE patients. Response to antibiotic therapy in chronic Lyme disease was associated with a significant decrease in the C4a level, whereas lack of response was associated with a significant increase in this marker. In contrast, AIDS patients had persistently increased C4a levels despite antiretroviral therapy. Lyme patients with positive single-photon emission computed tomographic (SPECT) scans had significantly lower C4a levels compared to Lyme patients with normal SPECT scan results. Patients with predominant musculoskeletal symptoms of Lyme disease have normal C3a and increased C4a levels. This pattern differs from the increase in both markers seen in acute Lyme disease, and C4a changes correlate with the response to therapy in chronic Lyme disease. C4a appears to be a valuable immunologic marker in patients with persistent symptoms of Lyme disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-Infective Agents - therapeutic use</subject><subject>Biomarkers - analysis</subject><subject>Borrelia</subject><subject>Child</subject><subject>Chronic Disease</subject><subject>Complement C3a - analysis</subject><subject>Complement C3a - immunology</subject><subject>Complement C4a - analysis</subject><subject>Complement C4a - immunology</subject><subject>Female</subject><subject>Humans</subject><subject>Lyme Disease - drug therapy</subject><subject>Lyme Disease - immunology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Radioimmunoassay</subject><subject>Young Adult</subject><issn>0300-9475</issn><issn>1365-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkctOwzAQRS0EoqXwC-AVu4TxI4m9YIHCq6gSSKVry0kmkCqPErei_XsSUsESvPFIPveOdEwIZeCz7lwtfSbCwBOghM8BlA-caeZvD8j45-GQjEEAeFpGwYicOLcEYIJH4piMOliCitSYXMdNtSqxwnpN56uyWNOXtsk26drRWFhq64zG0tKipvF729RFSme7Cult4dA6PCVHuS0dnu3vCVnc373Gj97s-WEa38y8VEaceVxqzFkuBCQJJlYnkoENlQ2zLJI2YTqzUqkAI0y46gbBuQy1QEhYGKapEhNyOfSu2uZjg25tqsKlWJa2xmbjTBgqpoTSf4IcuGZa9Y1qANO2ca7F3KzaorLtzjAwvWOzNL1K06s0vWPz7dhsu-j5fscmqTD7De6ldsD1AHwWJe7-XWzmT9N-6vIXQz63jbFvbeHMYs67zwMWRIxLIb4ATsiQ8A</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Stricker, R.B</creator><creator>Savely, V.R</creator><creator>Motanya, N.C</creator><creator>Giclas, P.C</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><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>7T5</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>2009</creationdate><title>Complement Split Products C3a and C4a in Chronic Lyme Disease</title><author>Stricker, R.B ; Savely, V.R ; Motanya, N.C ; Giclas, P.C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4721-249ef1f330bbeba9b410a68a6dd74ab19da4885e7eb288853224693e0b166cc83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Infective Agents - therapeutic use</topic><topic>Biomarkers - analysis</topic><topic>Borrelia</topic><topic>Child</topic><topic>Chronic Disease</topic><topic>Complement C3a - analysis</topic><topic>Complement C3a - immunology</topic><topic>Complement C4a - analysis</topic><topic>Complement C4a - immunology</topic><topic>Female</topic><topic>Humans</topic><topic>Lyme Disease - drug therapy</topic><topic>Lyme Disease - immunology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Radioimmunoassay</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stricker, R.B</creatorcontrib><creatorcontrib>Savely, V.R</creatorcontrib><creatorcontrib>Motanya, N.C</creatorcontrib><creatorcontrib>Giclas, P.C</creatorcontrib><collection>AGRIS</collection><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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Scandinavian journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stricker, R.B</au><au>Savely, V.R</au><au>Motanya, N.C</au><au>Giclas, P.C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complement Split Products C3a and C4a in Chronic Lyme Disease</atitle><jtitle>Scandinavian journal of immunology</jtitle><addtitle>Scand J Immunol</addtitle><date>2009</date><risdate>2009</risdate><volume>69</volume><issue>1</issue><spage>64</spage><epage>69</epage><pages>64-69</pages><issn>0300-9475</issn><eissn>1365-3083</eissn><abstract>Complement split products C3a and C4a are reportedly elevated in patients with acute Lyme disease. We have now examined these immunologic markers in patients with chronic Lyme disease compared to appropriate disease controls. The study population consisted of 29 healthy controls, 445 patients with chronic Lyme disease, 11 patients with systemic lupus erythematosus (SLE) and six patients with AIDS. The Lyme disease patients were divided according to predominant musculoskeletal symptoms (324 patients) or predominant neurologic symptoms (121 patients). C3a and C4a levels were measured by radioimmunoassay. All patients with chronic Lyme disease and AIDS had normal C3a levels compared to controls, whereas patients with SLE had significantly increased levels of this marker. Patients with predominant musculoskeletal symptoms of Lyme disease and AIDS patients had significantly increased levels of C4a compared to either controls, patients with predominant neurologic symptoms of Lyme disease or SLE patients. Response to antibiotic therapy in chronic Lyme disease was associated with a significant decrease in the C4a level, whereas lack of response was associated with a significant increase in this marker. In contrast, AIDS patients had persistently increased C4a levels despite antiretroviral therapy. Lyme patients with positive single-photon emission computed tomographic (SPECT) scans had significantly lower C4a levels compared to Lyme patients with normal SPECT scan results. Patients with predominant musculoskeletal symptoms of Lyme disease have normal C3a and increased C4a levels. This pattern differs from the increase in both markers seen in acute Lyme disease, and C4a changes correlate with the response to therapy in chronic Lyme disease. 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subjects | Adolescent Adult Aged Aged, 80 and over Anti-Infective Agents - therapeutic use Biomarkers - analysis Borrelia Child Chronic Disease Complement C3a - analysis Complement C3a - immunology Complement C4a - analysis Complement C4a - immunology Female Humans Lyme Disease - drug therapy Lyme Disease - immunology Male Middle Aged Radioimmunoassay Young Adult |
title | Complement Split Products C3a and C4a in Chronic Lyme Disease |
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