Activation of Synovial Fluid T Lymphocytes by 60‐Kd Heat‐Shock Proteins in Patients with Inflammatory synovitis

Objective. Synovial fluid lymphocytes from patients with rheumatoid arthritis and with other forms of inflammatory synovitis demonstrate enhanced proliferative responses to Mycobacterium tuberculosis antigens, in particular, the 65‐kd heat‐shock protein. There is a high degree of homology between th...

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Veröffentlicht in:Arthritis and rheumatism 1992-01, Vol.35 (1), p.43-48
Hauptverfasser: Pope, Richard M., Lovis, Rosa M., Gupta, Radhey S.
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container_title Arthritis and rheumatism
container_volume 35
creator Pope, Richard M.
Lovis, Rosa M.
Gupta, Radhey S.
description Objective. Synovial fluid lymphocytes from patients with rheumatoid arthritis and with other forms of inflammatory synovitis demonstrate enhanced proliferative responses to Mycobacterium tuberculosis antigens, in particular, the 65‐kd heat‐shock protein. There is a high degree of homology between the human and the mycobacterial 60‐kd family of heat‐shock proteins. These studies were performed to determine if the enhanced response to the mycobacterial 65‐kd heat‐shock protein was due to cross‐reactivity of an immune response generated against the human homolog. Methods. These studies were performed by in vitro culture of isolated synovial fluid mononuclear cells with crude and purified antigens. Results. The synovial fluid lymphocytes of a majority of patients with rheumatoid arthritis recognized the mycobacterial 65‐kd heat‐shock protein, as evidenced by T cell proliferation. In contrast, only 18% of all samples tested responded to a highly purified recombinant human 60‐kd heat‐shock protein. With only one exception, proliferative responses to the mycobacterial antigen were stronger than those to the human homolog. The proliferative responses generated against mycobacterial 65‐kd heat‐shock proteins from different sources were highly correlated. Conclusion. The findings suggest that the enhanced proliferative response to the mycobacterial 65‐kd heat‐shock protein noted in most patients with rheumatoid arthritis and other forms of inflammatory synovitis is not due to cross‐reactivity of an immune response directed against the human heat‐shock protein.
doi_str_mv 10.1002/art.1780350107
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Synovial fluid lymphocytes from patients with rheumatoid arthritis and with other forms of inflammatory synovitis demonstrate enhanced proliferative responses to Mycobacterium tuberculosis antigens, in particular, the 65‐kd heat‐shock protein. There is a high degree of homology between the human and the mycobacterial 60‐kd family of heat‐shock proteins. These studies were performed to determine if the enhanced response to the mycobacterial 65‐kd heat‐shock protein was due to cross‐reactivity of an immune response generated against the human homolog. Methods. These studies were performed by in vitro culture of isolated synovial fluid mononuclear cells with crude and purified antigens. Results. The synovial fluid lymphocytes of a majority of patients with rheumatoid arthritis recognized the mycobacterial 65‐kd heat‐shock protein, as evidenced by T cell proliferation. In contrast, only 18% of all samples tested responded to a highly purified recombinant human 60‐kd heat‐shock protein. With only one exception, proliferative responses to the mycobacterial antigen were stronger than those to the human homolog. The proliferative responses generated against mycobacterial 65‐kd heat‐shock proteins from different sources were highly correlated. Conclusion. The findings suggest that the enhanced proliferative response to the mycobacterial 65‐kd heat‐shock protein noted in most patients with rheumatoid arthritis and other forms of inflammatory synovitis is not due to cross‐reactivity of an immune response directed against the human heat‐shock protein.</description><identifier>ISSN: 0004-3591</identifier><identifier>EISSN: 1529-0131</identifier><identifier>DOI: 10.1002/art.1780350107</identifier><identifier>PMID: 1731814</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Antigens, Bacterial - immunology ; Antigens, Bacterial - physiology ; Arthritis, Rheumatoid - pathology ; Arthritis, Rheumatoid - physiopathology ; Cell Division - drug effects ; Cells, Cultured ; Heat-Shock Proteins - immunology ; Heat-Shock Proteins - pharmacology ; Humans ; Immunity, Cellular - drug effects ; Lymphocyte Activation - drug effects ; Lymphocyte Activation - physiology ; Monocytes - pathology ; Monocytes - physiology ; Mycobacterium tuberculosis - immunology ; Synovial Fluid - cytology ; Synovial Fluid - physiology ; Synovitis - pathology ; Synovitis - physiopathology ; T-Lymphocytes - drug effects ; T-Lymphocytes - physiology</subject><ispartof>Arthritis and rheumatism, 1992-01, Vol.35 (1), p.43-48</ispartof><rights>Copyright © 1992 American College of Rheumatology</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3157-1a237520d2fc0783623f4656ddfde58007a705708670c0aa6affb6b16ce2971f3</citedby><cites>FETCH-LOGICAL-c3157-1a237520d2fc0783623f4656ddfde58007a705708670c0aa6affb6b16ce2971f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fart.1780350107$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fart.1780350107$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1731814$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pope, Richard M.</creatorcontrib><creatorcontrib>Lovis, Rosa M.</creatorcontrib><creatorcontrib>Gupta, Radhey S.</creatorcontrib><title>Activation of Synovial Fluid T Lymphocytes by 60‐Kd Heat‐Shock Proteins in Patients with Inflammatory synovitis</title><title>Arthritis and rheumatism</title><addtitle>Arthritis Rheum</addtitle><description>Objective. Synovial fluid lymphocytes from patients with rheumatoid arthritis and with other forms of inflammatory synovitis demonstrate enhanced proliferative responses to Mycobacterium tuberculosis antigens, in particular, the 65‐kd heat‐shock protein. There is a high degree of homology between the human and the mycobacterial 60‐kd family of heat‐shock proteins. These studies were performed to determine if the enhanced response to the mycobacterial 65‐kd heat‐shock protein was due to cross‐reactivity of an immune response generated against the human homolog. Methods. These studies were performed by in vitro culture of isolated synovial fluid mononuclear cells with crude and purified antigens. Results. The synovial fluid lymphocytes of a majority of patients with rheumatoid arthritis recognized the mycobacterial 65‐kd heat‐shock protein, as evidenced by T cell proliferation. In contrast, only 18% of all samples tested responded to a highly purified recombinant human 60‐kd heat‐shock protein. 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Synovial fluid lymphocytes from patients with rheumatoid arthritis and with other forms of inflammatory synovitis demonstrate enhanced proliferative responses to Mycobacterium tuberculosis antigens, in particular, the 65‐kd heat‐shock protein. There is a high degree of homology between the human and the mycobacterial 60‐kd family of heat‐shock proteins. These studies were performed to determine if the enhanced response to the mycobacterial 65‐kd heat‐shock protein was due to cross‐reactivity of an immune response generated against the human homolog. Methods. These studies were performed by in vitro culture of isolated synovial fluid mononuclear cells with crude and purified antigens. Results. The synovial fluid lymphocytes of a majority of patients with rheumatoid arthritis recognized the mycobacterial 65‐kd heat‐shock protein, as evidenced by T cell proliferation. In contrast, only 18% of all samples tested responded to a highly purified recombinant human 60‐kd heat‐shock protein. With only one exception, proliferative responses to the mycobacterial antigen were stronger than those to the human homolog. The proliferative responses generated against mycobacterial 65‐kd heat‐shock proteins from different sources were highly correlated. Conclusion. The findings suggest that the enhanced proliferative response to the mycobacterial 65‐kd heat‐shock protein noted in most patients with rheumatoid arthritis and other forms of inflammatory synovitis is not due to cross‐reactivity of an immune response directed against the human heat‐shock protein.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>1731814</pmid><doi>10.1002/art.1780350107</doi><tpages>6</tpages></addata></record>
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subjects Antigens, Bacterial - immunology
Antigens, Bacterial - physiology
Arthritis, Rheumatoid - pathology
Arthritis, Rheumatoid - physiopathology
Cell Division - drug effects
Cells, Cultured
Heat-Shock Proteins - immunology
Heat-Shock Proteins - pharmacology
Humans
Immunity, Cellular - drug effects
Lymphocyte Activation - drug effects
Lymphocyte Activation - physiology
Monocytes - pathology
Monocytes - physiology
Mycobacterium tuberculosis - immunology
Synovial Fluid - cytology
Synovial Fluid - physiology
Synovitis - pathology
Synovitis - physiopathology
T-Lymphocytes - drug effects
T-Lymphocytes - physiology
title Activation of Synovial Fluid T Lymphocytes by 60‐Kd Heat‐Shock Proteins in Patients with Inflammatory synovitis
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