Identification of an IL-2 Binding Protein in the Saliva of the Lyme Disease Vector Tick, Ixodes scapularis

A potent inhibitor of mitogen-stimulated T cell proliferation exists in the saliva of several species of hard ticks, including the Lyme disease vector tick, Ixodes scapularis. Our characterization of this phenomenon has led to the identification of a possible mechanism for the T cell inhibitory acti...

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Veröffentlicht in:The Journal of immunology (1950) 2001-04, Vol.166 (7), p.4319-4326
Hauptverfasser: Gillespie, R. Dean, Dolan, Marc C, Piesman, Joseph, Titus, Richard G
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container_issue 7
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creator Gillespie, R. Dean
Dolan, Marc C
Piesman, Joseph
Titus, Richard G
description A potent inhibitor of mitogen-stimulated T cell proliferation exists in the saliva of several species of hard ticks, including the Lyme disease vector tick, Ixodes scapularis. Our characterization of this phenomenon has led to the identification of a possible mechanism for the T cell inhibitory activity of I. scapularis saliva. The T cell inhibitor can overcome stimulation of mouse spleen cells with anti-CD3 mAb; however, a direct and avid interaction with T cells does not appear to be necessary. Tick saliva inhibits a mouse IL-2 capture ELISA, suggesting that a soluble IL-2 binding factor is present in the saliva. This hypothesis was verified by using a direct binding assay in which plate-immobilized tick saliva was shown to bind both mouse and human IL-2. Elimination of the IL-2 binding capacity of saliva in the in vitro assays by trypsin digestion demonstrated that the IL-2 binding factor is a protein. These experiments comprise the first demonstration of the existence of such a secreted IL-2 binding protein from any parasite or pathogen. This arthropod salivary IL-2 binding capacity provides a simple mechanism for the suppression of T cell proliferation as well as for the activity of other immune effector cells that are responsive to IL-2 stimulation. Relevance of the tick T cell inhibitory activity to the human immune system is demonstrated by the ability of tick saliva to inhibit proliferation of human T cells and CTLL-2 cells grown in the presence of human IL-2.
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Elimination of the IL-2 binding capacity of saliva in the in vitro assays by trypsin digestion demonstrated that the IL-2 binding factor is a protein. These experiments comprise the first demonstration of the existence of such a secreted IL-2 binding protein from any parasite or pathogen. This arthropod salivary IL-2 binding capacity provides a simple mechanism for the suppression of T cell proliferation as well as for the activity of other immune effector cells that are responsive to IL-2 stimulation. 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Dean</creatorcontrib><creatorcontrib>Dolan, Marc C</creatorcontrib><creatorcontrib>Piesman, Joseph</creatorcontrib><creatorcontrib>Titus, Richard G</creatorcontrib><title>Identification of an IL-2 Binding Protein in the Saliva of the Lyme Disease Vector Tick, Ixodes scapularis</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>A potent inhibitor of mitogen-stimulated T cell proliferation exists in the saliva of several species of hard ticks, including the Lyme disease vector tick, Ixodes scapularis. Our characterization of this phenomenon has led to the identification of a possible mechanism for the T cell inhibitory activity of I. scapularis saliva. The T cell inhibitor can overcome stimulation of mouse spleen cells with anti-CD3 mAb; however, a direct and avid interaction with T cells does not appear to be necessary. Tick saliva inhibits a mouse IL-2 capture ELISA, suggesting that a soluble IL-2 binding factor is present in the saliva. This hypothesis was verified by using a direct binding assay in which plate-immobilized tick saliva was shown to bind both mouse and human IL-2. Elimination of the IL-2 binding capacity of saliva in the in vitro assays by trypsin digestion demonstrated that the IL-2 binding factor is a protein. These experiments comprise the first demonstration of the existence of such a secreted IL-2 binding protein from any parasite or pathogen. This arthropod salivary IL-2 binding capacity provides a simple mechanism for the suppression of T cell proliferation as well as for the activity of other immune effector cells that are responsive to IL-2 stimulation. 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Dean</creatorcontrib><creatorcontrib>Dolan, Marc C</creatorcontrib><creatorcontrib>Piesman, Joseph</creatorcontrib><creatorcontrib>Titus, Richard G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gillespie, R. 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The T cell inhibitor can overcome stimulation of mouse spleen cells with anti-CD3 mAb; however, a direct and avid interaction with T cells does not appear to be necessary. Tick saliva inhibits a mouse IL-2 capture ELISA, suggesting that a soluble IL-2 binding factor is present in the saliva. This hypothesis was verified by using a direct binding assay in which plate-immobilized tick saliva was shown to bind both mouse and human IL-2. Elimination of the IL-2 binding capacity of saliva in the in vitro assays by trypsin digestion demonstrated that the IL-2 binding factor is a protein. These experiments comprise the first demonstration of the existence of such a secreted IL-2 binding protein from any parasite or pathogen. This arthropod salivary IL-2 binding capacity provides a simple mechanism for the suppression of T cell proliferation as well as for the activity of other immune effector cells that are responsive to IL-2 stimulation. Relevance of the tick T cell inhibitory activity to the human immune system is demonstrated by the ability of tick saliva to inhibit proliferation of human T cells and CTLL-2 cells grown in the presence of human IL-2.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>11254684</pmid><doi>10.4049/jimmunol.166.7.4319</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Arthropod Vectors - immunology
Arthropod Vectors - metabolism
Binding, Competitive - immunology
Carrier Proteins - immunology
Carrier Proteins - metabolism
Cell Line
Enzyme-Linked Immunosorbent Assay
Female
Growth Inhibitors - immunology
Growth Inhibitors - metabolism
Growth Inhibitors - physiology
Humans
Immunosuppressive Agents - metabolism
Immunosuppressive Agents - pharmacology
interleukin 2-binding protein
Interleukin-2 - antagonists & inhibitors
Interleukin-2 - metabolism
Interleukin-2 - physiology
Ixodes - immunology
Ixodes - metabolism
Ixodes scapularis
Ixodidae
Lyme Disease - immunology
Lyme Disease - parasitology
Lymphocyte Activation - immunology
Mice
Mice, Inbred C57BL
Protein Binding - immunology
Rabbits
Recombinant Proteins - metabolism
Saliva - immunology
Saliva - metabolism
Salivary Proteins and Peptides - immunology
Salivary Proteins and Peptides - metabolism
Species Specificity
T-Lymphocytes - cytology
T-Lymphocytes - immunology
title Identification of an IL-2 Binding Protein in the Saliva of the Lyme Disease Vector Tick, Ixodes scapularis
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