The biological and immunomodulatory properties of sand fly saliva and its role in the establishment of Leishmania infections.
暂无分享,去创建一个
[1] Y. Belkaid,et al. Delayed-type hypersensitivity to Phlebotomus papatasi sand fly bite: An adaptive response induced by the fly? , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[2] J. Ribeiro,et al. The salivary adenosine deaminase from the sand fly Lutzomyia longipalpis. , 2000, Experimental parasitology.
[3] R. Charlab,et al. The salivary 5′-nucleotidase/phosphodiesterase of the hematophagus sand lutzomyia fly, Lutzomyia longipalpis , 2000 .
[4] J. Ribeiro,et al. Salivary amylase activity of the phlebotomine sand fly, Lutzomyia longipalpis. , 2000, Insect biochemistry and molecular biology.
[5] C. Szabó,et al. Inosine Inhibits Inflammatory Cytokine Production by a Posttranscriptional Mechanism and Protects Against Endotoxin-Induced Shock1 , 2000, The Journal of Immunology.
[6] G. Chrousos,et al. Ligand-Activation of the Adenosine A2a Receptors Inhibits IL-12 Production by Human Monocytes , 2000, The Journal of Immunology.
[7] J. Ribeiro,et al. Toward an understanding of the biochemical and pharmacological complexity of the saliva of a hematophagous sand fly Lutzomyia longipalpis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[8] A. Satoskar,et al. Leishmania species: models of intracellular parasitism. , 1999, Journal of cell science.
[9] Z. Zídek. Adenosine - cyclic AMP pathways and cytokine expression. , 1999, European cytokine network.
[10] S. Denda,et al. Functional Characterization of Structural Alterations in the Sequence of the Vasodilatory Peptide Maxadilan Yields a Pituitary Adenylate Cyclase-activating Peptide Type 1 Receptor-specific Antagonist* , 1999, The Journal of Biological Chemistry.
[11] S. Wikel. Tick modulation of host immunity: an important factor in pathogen transmission. , 1999, International journal for parasitology.
[12] J. Ribeiro,et al. Salivary glands of the sand fly Phlebotomus papatasi contain pharmacologically active amounts of adenosine and 5'-AMP. , 1999, The Journal of experimental biology.
[13] A. James,et al. Variation in the salivary peptide, maxadilan, from species in the Lutzomyia longipalpis complex , 1999, Insect molecular biology.
[14] S. Wikel. MODULATION OF THE HOST IMMUNE SYSTEM BY ECTOPARASITIC ARTHROPODS , 1999 .
[15] W. Born,et al. Maxadilan interacts with receptors for pituitary adenylyl cyclase activating peptide in human SH-SY5Y and SK-N-MC neuroblastoma cells , 1999, Neuropeptides.
[16] M. Horton,et al. Hyaluronan Fragments Synergize with Interferon-γ to Induce the C-X-C Chemokines Mig and Interferon-inducible Protein-10 in Mouse Macrophages* , 1998, The Journal of Biological Chemistry.
[17] Y. Belkaid,et al. Development of a Natural Model of Cutaneous Leishmaniasis: Powerful Effects of Vector Saliva and Saliva Preexposure on the Long-Term Outcome of Leishmania major Infection in the Mouse Ear Dermis , 1998, The Journal of experimental medicine.
[18] M. Mbow,et al. Phlebotomus papatasi sand fly salivary gland lysate down-regulates a Th1, but up-regulates a Th2, response in mice infected with Leishmania major. , 1998, Journal of immunology.
[19] E. Vizi,et al. An agonist of adenosine A3 receptors decreases interleukin-12 and interferon-gamma production and prevents lethality in endotoxemic mice. , 1998, European journal of pharmacology.
[20] A. Satoskar,et al. The PACAP‐type I receptor agonist maxadilan from sand fly saliva protects mice against lethal endotoxemia by a mechanism partially dependent on IL‐10 , 1998, European journal of immunology.
[21] R. Titus. Salivary gland lysate from the sand fly Lutzomyia longipalpis suppresses the immune response of mice to sheep red blood cells in vivo and concanavalin A in vitro. , 1998, Experimental parasitology.
[22] A. Warburg,et al. Phlebotomus papatasi Saliva Inhibits Protein Phosphatase Activity and Nitric Oxide Production by Murine Macrophages , 1998, Infection and Immunity.
[23] M. Horton,et al. Regulation of hyaluronan-induced chemokine gene expression by IL-10 and IFN-gamma in mouse macrophages. , 1998, Journal of immunology.
[24] M. Soares,et al. The vasoactive peptide maxadilan from sand fly saliva inhibits TNF-alpha and induces IL-6 by mouse macrophages through interaction with the pituitary adenylate cyclase-activating polypeptide (PACAP) receptor. , 1998, Journal of immunology.
[25] R. Titus,et al. Histologic characterization of experimental cutaneous leishmaniasis in mice infected with Leishmania braziliensis in the presence or absence of sand fly vector salivary gland lysate. , 1998, The Journal of parasitology.
[26] M. Horton,et al. Hyaluronan Fragments Induce Nitric-oxide Synthase in Murine Macrophages through a Nuclear Factor κB-dependent Mechanism* , 1997, The Journal of Biological Chemistry.
[27] E. Lerner,et al. Maxadilan, the Vasodilator from Sand Flies, Is a Specific Pituitary Adenylate Cyclase Activating Peptide Type I Receptor Agonist* , 1997, The Journal of Biological Chemistry.
[28] E. Lerner,et al. Receptors for the vasodilator maxadilan are expressed on selected neural crest and smooth muscle-derived cells. , 1996, Insect biochemistry and molecular biology.
[29] R. Titus,et al. Effects of sand fly vector saliva on development of cutaneous lesions and the immune response to Leishmania braziliensis in BALB/c mice , 1996, Infection and immunity.
[30] E. Vizi,et al. Adenosine receptor agonists differentially regulate IL-10, TNF-alpha, and nitric oxide production in RAW 264.7 macrophages and in endotoxemic mice. , 1996, Journal of immunology.
[31] M. Burdick,et al. Hyaluronan (HA) fragments induce chemokine gene expression in alveolar macrophages. The role of HA size and CD44. , 1996, The Journal of clinical investigation.
[32] J. Loscalzo,et al. Vasodilatory properties of recombinant maxadilan. , 1996, The American journal of physiology.
[33] F. Liew,et al. Immunology of murine leishmaniasis. , 1996, Clinics in dermatology.
[34] A. James,et al. Salivary gland anticoagulants in culicine and anopheline mosquitoes (Diptera:Culicidae). , 1996, Journal of medical entomology.
[35] R. Granstein,et al. Immunomodulatory properties of maxadilan, the vasodilator peptide from sand fly salivary gland extracts. , 1996, The American journal of tropical medicine and hygiene.
[36] O. Moine,et al. Adenosine enhances IL-10 secretion by human monocytes. , 1996, Journal of immunology.
[37] R. Titus,et al. Sand fly vector saliva selectively modulates macrophage functions that inhibit killing of Leishmania major and nitric oxide production. , 1995, Journal of immunology.
[38] J. Githure,et al. The chemotactic effect of Phlebotomus duboscqi (Diptera: Psychodidae) salivary gland lysates to murine monocytes. , 1995, Acta tropica.
[39] J. Ribeiro,et al. Blood-feeding arthropods: live syringes or invertebrate pharmacologists? , 1995, Infectious agents and disease.
[40] R. Tesh,et al. Leishmania amazonensis: sensitivity of different promastigote morphotypes to salivary gland homogenates of the sand fly Lutzomyia longipalpis. , 1995, Experimental parasitology.
[41] J. Loscalzo,et al. Vasorelaxant and second messenger effects of maxadilan. , 1995, The Journal of pharmacology and experimental therapeutics.
[42] S. Hourani,et al. Characterization of adenosine receptors in the rat isolated aorta. , 1994, General pharmacology.
[43] R. Titus,et al. Saliva of Lutzomyia longipalpis sibling species differs in its composition and capacity to enhance leishmaniasis. , 1994, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[44] D. Champagne. The role of salivary vasodilators in bloodfeeding and parasite transmission. , 1994, Parasitology today.
[45] R. Titus,et al. Salivary gland material from the sand fly Lutzomyia longipalpis has an inhibitory effect on macrophage function in vitro , 1993, Parasite immunology.
[46] J. Ribeiro,et al. Cytostatic effect of Lutzomyia longipalpis salivary gland homogenates on Leishmania parasites. , 1993, The American journal of tropical medicine and hygiene.
[47] C. Shoemaker,et al. Maxadilan. Cloning and functional expression of the gene encoding this potent vasodilator peptide. , 1992, The Journal of biological chemistry.
[48] M. Lerner,et al. Isolation of maxadilan, a potent vasodilatory peptide from the salivary glands of the sand fly Lutzomyia longipalpis. , 1991, The Journal of biological chemistry.
[49] J. Ribeiro,et al. Analysis of enhancing effect of sand fly saliva on Leishmania infection in mice , 1991, Infection and immunity.
[50] R. Tesh,et al. A mouse model of Leishmania braziliensis braziliensis infection produced by coinjection with sand fly saliva , 1991, The Journal of experimental medicine.
[51] R. Titus,et al. The role of vector saliva in transmission of arthropod-borne disease. , 1990, Parasitology today.
[52] L. Ryan. Multiple forced feeding of individual sandflies. , 1989, Transactions of the Royal Society of Tropical Medicine and Hygiene.
[53] J. Ribeiro,et al. Vector saliva and its role in parasite transmission. , 1989, Experimental parasitology.
[54] R. Titus,et al. Peptides encoded by the calcitonin gene inhibit macrophage function. , 1989, Journal of immunology.
[55] R. Tesh,et al. A novel vasodilatory peptide from the salivary glands of the sand fly Lutzomyia longipalpis. , 1989, Science.
[56] R. Tesh,et al. Salivary apyrase activity of some old world phlebotomine sand flies , 1989 .
[57] M. Collis,et al. The vasodilator role of adenosine. , 1989, Pharmacology & therapeutics.
[58] R. Titus,et al. Salivary gland lysates from the sand fly Lutzomyia longipalpis enhance Leishmania infectivity. , 1988, Science.
[59] J. Ribeiro. Vector salivation and parasite transmission. , 1987, Memorias do Instituto Oswaldo Cruz.
[60] J. Ribeiro. Role of saliva in blood-feeding by arthropods. , 1987, Annual review of entomology.
[61] Y. Schlein,et al. The effect of post-bloodmeal nutrition of Phlebotomus papatasi on the transmission of Leishmania major. , 1986, The American journal of tropical medicine and hygiene.
[62] A. Spielman,et al. Blood-finding strategy of a capillary-feeding sandfly, Lutzomyia longipalpis. , 1986, Comparative biochemistry and physiology. A, Comparative physiology.
[63] R. Beach,et al. Modification of sand fly biting behavior by Leishmania leads to increased parasite transmission. , 1985, The American journal of tropical medicine and hygiene.
[64] Krampitz He. [The Elba triad: harara, light dermatoses, leishmaniasis. The ecological background]. , 1981 .
[65] S. Wikel. The induction of host resistance to tick infestation with a salivary gland antigen. , 1981, The American journal of tropical medicine and hygiene.
[66] P. Ready,et al. Leishmania in phlebotomid sandflies - IV. The transmission of Leishmania mexicana amazonensis to hamsters by the bite of experimentally infected Lutzomyia longipalpis , 1977, Proceedings of the Royal Society of London. Series B. Biological Sciences.
[67] O. Theodor. A study of the reaction to phlebotomus bites with some remarks on “Harara” , 1935 .
[68] H. Shortt,et al. The Method of Feeding of Phlebotomus argentipes with Relation to its Bearing on the Transmission of Kala-Azar. , 1928 .
[69] O. Theodor,et al. The Mouth Parts, Alimentary Tract, and Salivary Apparatus of the Female in Phlebotomus Papatasii , 1926 .