Human_Leishmaniasis@cytokines.bahia.br

The cell-mediated immune response is critical in the resistance to and recovery from leishmaniasis. Cytokines are central elements in mounting an immune response and have received a great deal of attention in both human and experimental leishmaniasis. IFN-<FONT FACE="Symbol">g</font> is responsible for macrophage activation leading to leishmanicidal mechanisms. Understanding the balance of cytokines that lead to enhanced production of or synergize with IFN-<FONT FACE="Symbol">g</font>, and those cytokines that counterbalance its effects is fundamental for developing rational immunotherapeutic or immunoprophylactic approaches to leishmaniasis. Here we focus on the cytokine balance in human leishmaniasis, particularly IL-10 as an IFN-<FONT FACE="Symbol">g</font> opposing cytokine, and IL-12 as an IFN-<FONT FACE="Symbol">g</font> inducer. The effects of these cytokines were evaluated in terms of several parameters of the human immune response. IL-10 reduced lymphocyte proliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity of responsive human peripheral blood mononuclear cells. Neutralization of IL-10 led to partial restoration of lymphoproliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity in unresponsive visceral leishmaniasis patients. IL-12 also restored the responses of peripheral blood mononuclear cells from visceral leishmaniasis patients. The responses obtained with IL-12 are higher than those obtained with anti-IL-10, even when anti-IL-10 is combined with anti-IL-4

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Main Authors: Barral-Netto,M., Brodskyn,C., Carvalho,E.M., Barral,A.
Format: Digital revista
Language:English
Published: Associação Brasileira de Divulgação Científica 1998
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000100021
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spelling oai:scielo:S0100-879X19980001000211998-10-07Human_Leishmaniasis@cytokines.bahia.brBarral-Netto,M.Brodskyn,C.Carvalho,E.M.Barral,A. cytokines human leishmaniasis immunoregulation IL-12 IL-10 The cell-mediated immune response is critical in the resistance to and recovery from leishmaniasis. Cytokines are central elements in mounting an immune response and have received a great deal of attention in both human and experimental leishmaniasis. IFN-<FONT FACE="Symbol">g</font> is responsible for macrophage activation leading to leishmanicidal mechanisms. Understanding the balance of cytokines that lead to enhanced production of or synergize with IFN-<FONT FACE="Symbol">g</font>, and those cytokines that counterbalance its effects is fundamental for developing rational immunotherapeutic or immunoprophylactic approaches to leishmaniasis. Here we focus on the cytokine balance in human leishmaniasis, particularly IL-10 as an IFN-<FONT FACE="Symbol">g</font> opposing cytokine, and IL-12 as an IFN-<FONT FACE="Symbol">g</font> inducer. The effects of these cytokines were evaluated in terms of several parameters of the human immune response. IL-10 reduced lymphocyte proliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity of responsive human peripheral blood mononuclear cells. Neutralization of IL-10 led to partial restoration of lymphoproliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity in unresponsive visceral leishmaniasis patients. IL-12 also restored the responses of peripheral blood mononuclear cells from visceral leishmaniasis patients. The responses obtained with IL-12 are higher than those obtained with anti-IL-10, even when anti-IL-10 is combined with anti-IL-4info:eu-repo/semantics/openAccessAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research v.31 n.1 19981998-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000100021en10.1590/S0100-879X1998000100021
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countrycode BR
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databasecode rev-scielo-br
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region America del Sur
libraryname SciELO
language English
format Digital
author Barral-Netto,M.
Brodskyn,C.
Carvalho,E.M.
Barral,A.
spellingShingle Barral-Netto,M.
Brodskyn,C.
Carvalho,E.M.
Barral,A.
Human_Leishmaniasis@cytokines.bahia.br
author_facet Barral-Netto,M.
Brodskyn,C.
Carvalho,E.M.
Barral,A.
author_sort Barral-Netto,M.
title Human_Leishmaniasis@cytokines.bahia.br
title_short Human_Leishmaniasis@cytokines.bahia.br
title_full Human_Leishmaniasis@cytokines.bahia.br
title_fullStr Human_Leishmaniasis@cytokines.bahia.br
title_full_unstemmed Human_Leishmaniasis@cytokines.bahia.br
title_sort human_leishmaniasis@cytokines.bahia.br
description The cell-mediated immune response is critical in the resistance to and recovery from leishmaniasis. Cytokines are central elements in mounting an immune response and have received a great deal of attention in both human and experimental leishmaniasis. IFN-<FONT FACE="Symbol">g</font> is responsible for macrophage activation leading to leishmanicidal mechanisms. Understanding the balance of cytokines that lead to enhanced production of or synergize with IFN-<FONT FACE="Symbol">g</font>, and those cytokines that counterbalance its effects is fundamental for developing rational immunotherapeutic or immunoprophylactic approaches to leishmaniasis. Here we focus on the cytokine balance in human leishmaniasis, particularly IL-10 as an IFN-<FONT FACE="Symbol">g</font> opposing cytokine, and IL-12 as an IFN-<FONT FACE="Symbol">g</font> inducer. The effects of these cytokines were evaluated in terms of several parameters of the human immune response. IL-10 reduced lymphocyte proliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity of responsive human peripheral blood mononuclear cells. Neutralization of IL-10 led to partial restoration of lymphoproliferation, IFN-<FONT FACE="Symbol">g</font> production and cytotoxic activity in unresponsive visceral leishmaniasis patients. IL-12 also restored the responses of peripheral blood mononuclear cells from visceral leishmaniasis patients. The responses obtained with IL-12 are higher than those obtained with anti-IL-10, even when anti-IL-10 is combined with anti-IL-4
publisher Associação Brasileira de Divulgação Científica
publishDate 1998
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1998000100021
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