author_facet Lieke, T
Nylén, S
Eidsmo, L
McMaster, W R
Mohammadi, A M
Khamesipour, A
Berg, L
Akuffo, H
Lieke, T
Nylén, S
Eidsmo, L
McMaster, W R
Mohammadi, A M
Khamesipour, A
Berg, L
Akuffo, H
author Lieke, T
Nylén, S
Eidsmo, L
McMaster, W R
Mohammadi, A M
Khamesipour, A
Berg, L
Akuffo, H
spellingShingle Lieke, T
Nylén, S
Eidsmo, L
McMaster, W R
Mohammadi, A M
Khamesipour, A
Berg, L
Akuffo, H
Clinical and Experimental Immunology
Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
Immunology
Immunology and Allergy
author_sort lieke, t
spelling Lieke, T Nylén, S Eidsmo, L McMaster, W R Mohammadi, A M Khamesipour, A Berg, L Akuffo, H 0009-9104 1365-2249 Oxford University Press (OUP) Immunology Immunology and Allergy http://dx.doi.org/10.1111/j.1365-2249.2008.03687.x <jats:title>Summary</jats:title><jats:p>Natural killer (NK) cells contribute to immunity as the first line of defence in numerous infections by early cytokine secretion and cytotoxicity. In Leishmania infection, NK cells contribute with interferon-γ and may assist in directing the immune response towards T helper type 1, which is essential for successful control of the parasites. Thus, NK cells may play an important role in both resistance and control of the infection. However, during Leishmania infection NK cells show signs of suppression. To explore the reason for this suppression, we exposed naive and interleukin (IL)-2 activated NK cells directly to promastigotes of Leishmania major in vitro. As a rapid consequence of contact between naive NK cells and promastigotes, expression of NK cell receptors show significant changes. We identify one of the major surface molecules of promastigotes, glycoprotein (gp) 63, as an important agent for these suppressive effects by using promastigotes of a gp63ko strain of L. major. Furthermore, proliferation of IL-2-activated purified NK cells is suppressed after exposure to the wild-type but not to gp63ko promastigotes. However, gp63ko L. major induced no NK cell proliferation when NK cells were co-cultured with peripheral blood mononuclear cells populations such as CD14+ monocytes or T cells.</jats:p> Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation Clinical and Experimental Immunology
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title Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_unstemmed Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_full Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_fullStr Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_full_unstemmed Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_short Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_sort leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
topic Immunology
Immunology and Allergy
url http://dx.doi.org/10.1111/j.1365-2249.2008.03687.x
publishDate 2008
physical 221-230
description <jats:title>Summary</jats:title><jats:p>Natural killer (NK) cells contribute to immunity as the first line of defence in numerous infections by early cytokine secretion and cytotoxicity. In Leishmania infection, NK cells contribute with interferon-γ and may assist in directing the immune response towards T helper type 1, which is essential for successful control of the parasites. Thus, NK cells may play an important role in both resistance and control of the infection. However, during Leishmania infection NK cells show signs of suppression. To explore the reason for this suppression, we exposed naive and interleukin (IL)-2 activated NK cells directly to promastigotes of Leishmania major in vitro. As a rapid consequence of contact between naive NK cells and promastigotes, expression of NK cell receptors show significant changes. We identify one of the major surface molecules of promastigotes, glycoprotein (gp) 63, as an important agent for these suppressive effects by using promastigotes of a gp63ko strain of L. major. Furthermore, proliferation of IL-2-activated purified NK cells is suppressed after exposure to the wild-type but not to gp63ko promastigotes. However, gp63ko L. major induced no NK cell proliferation when NK cells were co-cultured with peripheral blood mononuclear cells populations such as CD14+ monocytes or T cells.</jats:p>
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author Lieke, T, Nylén, S, Eidsmo, L, McMaster, W R, Mohammadi, A M, Khamesipour, A, Berg, L, Akuffo, H
author_facet Lieke, T, Nylén, S, Eidsmo, L, McMaster, W R, Mohammadi, A M, Khamesipour, A, Berg, L, Akuffo, H, Lieke, T, Nylén, S, Eidsmo, L, McMaster, W R, Mohammadi, A M, Khamesipour, A, Berg, L, Akuffo, H
author_sort lieke, t
container_issue 2
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container_title Clinical and Experimental Immunology
container_volume 153
description <jats:title>Summary</jats:title><jats:p>Natural killer (NK) cells contribute to immunity as the first line of defence in numerous infections by early cytokine secretion and cytotoxicity. In Leishmania infection, NK cells contribute with interferon-γ and may assist in directing the immune response towards T helper type 1, which is essential for successful control of the parasites. Thus, NK cells may play an important role in both resistance and control of the infection. However, during Leishmania infection NK cells show signs of suppression. To explore the reason for this suppression, we exposed naive and interleukin (IL)-2 activated NK cells directly to promastigotes of Leishmania major in vitro. As a rapid consequence of contact between naive NK cells and promastigotes, expression of NK cell receptors show significant changes. We identify one of the major surface molecules of promastigotes, glycoprotein (gp) 63, as an important agent for these suppressive effects by using promastigotes of a gp63ko strain of L. major. Furthermore, proliferation of IL-2-activated purified NK cells is suppressed after exposure to the wild-type but not to gp63ko promastigotes. However, gp63ko L. major induced no NK cell proliferation when NK cells were co-cultured with peripheral blood mononuclear cells populations such as CD14+ monocytes or T cells.</jats:p>
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spelling Lieke, T Nylén, S Eidsmo, L McMaster, W R Mohammadi, A M Khamesipour, A Berg, L Akuffo, H 0009-9104 1365-2249 Oxford University Press (OUP) Immunology Immunology and Allergy http://dx.doi.org/10.1111/j.1365-2249.2008.03687.x <jats:title>Summary</jats:title><jats:p>Natural killer (NK) cells contribute to immunity as the first line of defence in numerous infections by early cytokine secretion and cytotoxicity. In Leishmania infection, NK cells contribute with interferon-γ and may assist in directing the immune response towards T helper type 1, which is essential for successful control of the parasites. Thus, NK cells may play an important role in both resistance and control of the infection. However, during Leishmania infection NK cells show signs of suppression. To explore the reason for this suppression, we exposed naive and interleukin (IL)-2 activated NK cells directly to promastigotes of Leishmania major in vitro. As a rapid consequence of contact between naive NK cells and promastigotes, expression of NK cell receptors show significant changes. We identify one of the major surface molecules of promastigotes, glycoprotein (gp) 63, as an important agent for these suppressive effects by using promastigotes of a gp63ko strain of L. major. Furthermore, proliferation of IL-2-activated purified NK cells is suppressed after exposure to the wild-type but not to gp63ko promastigotes. However, gp63ko L. major induced no NK cell proliferation when NK cells were co-cultured with peripheral blood mononuclear cells populations such as CD14+ monocytes or T cells.</jats:p> Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation Clinical and Experimental Immunology
spellingShingle Lieke, T, Nylén, S, Eidsmo, L, McMaster, W R, Mohammadi, A M, Khamesipour, A, Berg, L, Akuffo, H, Clinical and Experimental Immunology, Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation, Immunology, Immunology and Allergy
title Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_full Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_fullStr Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_full_unstemmed Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_short Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_sort leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
title_unstemmed Leishmania surface protein gp63 binds directly to human natural killer cells and inhibits proliferation
topic Immunology, Immunology and Allergy
url http://dx.doi.org/10.1111/j.1365-2249.2008.03687.x