author_facet Bezerra, Caroline A.
Cardoso, Thiago M.
Giudice, Angela
Porto, Aurélia F.
Santos, Silvane B.
Carvalho, Edgar M.
Bacellar, Olívia
Bezerra, Caroline A.
Cardoso, Thiago M.
Giudice, Angela
Porto, Aurélia F.
Santos, Silvane B.
Carvalho, Edgar M.
Bacellar, Olívia
author Bezerra, Caroline A.
Cardoso, Thiago M.
Giudice, Angela
Porto, Aurélia F.
Santos, Silvane B.
Carvalho, Edgar M.
Bacellar, Olívia
spellingShingle Bezerra, Caroline A.
Cardoso, Thiago M.
Giudice, Angela
Porto, Aurélia F.
Santos, Silvane B.
Carvalho, Edgar M.
Bacellar, Olívia
Scandinavian Journal of Immunology
Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
Immunology
General Medicine
author_sort bezerra, caroline a.
spelling Bezerra, Caroline A. Cardoso, Thiago M. Giudice, Angela Porto, Aurélia F. Santos, Silvane B. Carvalho, Edgar M. Bacellar, Olívia 0300-9475 1365-3083 Wiley Immunology General Medicine http://dx.doi.org/10.1111/j.1365-3083.2011.02579.x <jats:title>Abstract</jats:title><jats:p>Human T cell lymphotropic virus type‐1 (HTLV‐1) induces activation and spontaneous proliferation of T cells with production of type‐1 pro‐inflammatory cytokines. It modifies the immune response to other antigens and increases susceptibility to infectious diseases. However, little is known about innate immunity in HTLV‐1 infection. HTLV‐1‐infected individuals have higher spontaneous neutrophil activation than HTLV‐1‐seronegative individuals, as shown by the nitroblue tetrazolium (NBT) assay. This study was conducted to evaluate neutrophil function in HTLV‐1‐infected individuals. Participants in the study included 18 HTLV‐1‐infected individuals and 14 HTLV‐1‐seronegative controls. We evaluated the ability of neutrophils (PMNs) to control a parasite infection, to produce peroxynitrite, cytokines and chemokines and to express activation markers in cultures when stimulated with LPS or infected with <jats:italic>Leishmania</jats:italic>. When compared with the control group, there was no difference in the percentage of PMNs infected with <jats:italic>Leishmania</jats:italic> or in the number of amastigotes/100 PMNs in HTLV‐1‐infected individuals. The microbicidal activity of the PMNs and the levels of CXCL8 and CCL4 released by these cells did not show a difference between HTLV‐1‐infected individuals and the control group. In both the HTLV‐1 group and the control group, infection with <jats:italic>Leishmania</jats:italic> or stimulation of PMNs led to cellular activation. These observations suggest that neutrophils from HTLV‐1‐infected individuals have preserved their ability to become activated and to produce chemokines and peroxynitrite after stimulation and that the susceptibility to infection by intracellular <jats:italic>Leishmania amazonensis</jats:italic> in HTLV‐1‐infected individuals does not depend on impairment of neutrophil function.</jats:p> Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals Scandinavian Journal of Immunology
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title Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_unstemmed Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_full Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_fullStr Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_full_unstemmed Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_short Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_sort evaluation of the microbicidal activity and cytokines/chemokines profile released by neutrophils from htlv‐1‐infected individuals
topic Immunology
General Medicine
url http://dx.doi.org/10.1111/j.1365-3083.2011.02579.x
publishDate 2011
physical 310-317
description <jats:title>Abstract</jats:title><jats:p>Human T cell lymphotropic virus type‐1 (HTLV‐1) induces activation and spontaneous proliferation of T cells with production of type‐1 pro‐inflammatory cytokines. It modifies the immune response to other antigens and increases susceptibility to infectious diseases. However, little is known about innate immunity in HTLV‐1 infection. HTLV‐1‐infected individuals have higher spontaneous neutrophil activation than HTLV‐1‐seronegative individuals, as shown by the nitroblue tetrazolium (NBT) assay. This study was conducted to evaluate neutrophil function in HTLV‐1‐infected individuals. Participants in the study included 18 HTLV‐1‐infected individuals and 14 HTLV‐1‐seronegative controls. We evaluated the ability of neutrophils (PMNs) to control a parasite infection, to produce peroxynitrite, cytokines and chemokines and to express activation markers in cultures when stimulated with LPS or infected with <jats:italic>Leishmania</jats:italic>. When compared with the control group, there was no difference in the percentage of PMNs infected with <jats:italic>Leishmania</jats:italic> or in the number of amastigotes/100 PMNs in HTLV‐1‐infected individuals. The microbicidal activity of the PMNs and the levels of CXCL8 and CCL4 released by these cells did not show a difference between HTLV‐1‐infected individuals and the control group. In both the HTLV‐1 group and the control group, infection with <jats:italic>Leishmania</jats:italic> or stimulation of PMNs led to cellular activation. These observations suggest that neutrophils from HTLV‐1‐infected individuals have preserved their ability to become activated and to produce chemokines and peroxynitrite after stimulation and that the susceptibility to infection by intracellular <jats:italic>Leishmania amazonensis</jats:italic> in HTLV‐1‐infected individuals does not depend on impairment of neutrophil function.</jats:p>
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author Bezerra, Caroline A., Cardoso, Thiago M., Giudice, Angela, Porto, Aurélia F., Santos, Silvane B., Carvalho, Edgar M., Bacellar, Olívia
author_facet Bezerra, Caroline A., Cardoso, Thiago M., Giudice, Angela, Porto, Aurélia F., Santos, Silvane B., Carvalho, Edgar M., Bacellar, Olívia, Bezerra, Caroline A., Cardoso, Thiago M., Giudice, Angela, Porto, Aurélia F., Santos, Silvane B., Carvalho, Edgar M., Bacellar, Olívia
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container_title Scandinavian Journal of Immunology
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description <jats:title>Abstract</jats:title><jats:p>Human T cell lymphotropic virus type‐1 (HTLV‐1) induces activation and spontaneous proliferation of T cells with production of type‐1 pro‐inflammatory cytokines. It modifies the immune response to other antigens and increases susceptibility to infectious diseases. However, little is known about innate immunity in HTLV‐1 infection. HTLV‐1‐infected individuals have higher spontaneous neutrophil activation than HTLV‐1‐seronegative individuals, as shown by the nitroblue tetrazolium (NBT) assay. This study was conducted to evaluate neutrophil function in HTLV‐1‐infected individuals. Participants in the study included 18 HTLV‐1‐infected individuals and 14 HTLV‐1‐seronegative controls. We evaluated the ability of neutrophils (PMNs) to control a parasite infection, to produce peroxynitrite, cytokines and chemokines and to express activation markers in cultures when stimulated with LPS or infected with <jats:italic>Leishmania</jats:italic>. When compared with the control group, there was no difference in the percentage of PMNs infected with <jats:italic>Leishmania</jats:italic> or in the number of amastigotes/100 PMNs in HTLV‐1‐infected individuals. The microbicidal activity of the PMNs and the levels of CXCL8 and CCL4 released by these cells did not show a difference between HTLV‐1‐infected individuals and the control group. In both the HTLV‐1 group and the control group, infection with <jats:italic>Leishmania</jats:italic> or stimulation of PMNs led to cellular activation. These observations suggest that neutrophils from HTLV‐1‐infected individuals have preserved their ability to become activated and to produce chemokines and peroxynitrite after stimulation and that the susceptibility to infection by intracellular <jats:italic>Leishmania amazonensis</jats:italic> in HTLV‐1‐infected individuals does not depend on impairment of neutrophil function.</jats:p>
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spelling Bezerra, Caroline A. Cardoso, Thiago M. Giudice, Angela Porto, Aurélia F. Santos, Silvane B. Carvalho, Edgar M. Bacellar, Olívia 0300-9475 1365-3083 Wiley Immunology General Medicine http://dx.doi.org/10.1111/j.1365-3083.2011.02579.x <jats:title>Abstract</jats:title><jats:p>Human T cell lymphotropic virus type‐1 (HTLV‐1) induces activation and spontaneous proliferation of T cells with production of type‐1 pro‐inflammatory cytokines. It modifies the immune response to other antigens and increases susceptibility to infectious diseases. However, little is known about innate immunity in HTLV‐1 infection. HTLV‐1‐infected individuals have higher spontaneous neutrophil activation than HTLV‐1‐seronegative individuals, as shown by the nitroblue tetrazolium (NBT) assay. This study was conducted to evaluate neutrophil function in HTLV‐1‐infected individuals. Participants in the study included 18 HTLV‐1‐infected individuals and 14 HTLV‐1‐seronegative controls. We evaluated the ability of neutrophils (PMNs) to control a parasite infection, to produce peroxynitrite, cytokines and chemokines and to express activation markers in cultures when stimulated with LPS or infected with <jats:italic>Leishmania</jats:italic>. When compared with the control group, there was no difference in the percentage of PMNs infected with <jats:italic>Leishmania</jats:italic> or in the number of amastigotes/100 PMNs in HTLV‐1‐infected individuals. The microbicidal activity of the PMNs and the levels of CXCL8 and CCL4 released by these cells did not show a difference between HTLV‐1‐infected individuals and the control group. In both the HTLV‐1 group and the control group, infection with <jats:italic>Leishmania</jats:italic> or stimulation of PMNs led to cellular activation. These observations suggest that neutrophils from HTLV‐1‐infected individuals have preserved their ability to become activated and to produce chemokines and peroxynitrite after stimulation and that the susceptibility to infection by intracellular <jats:italic>Leishmania amazonensis</jats:italic> in HTLV‐1‐infected individuals does not depend on impairment of neutrophil function.</jats:p> Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals Scandinavian Journal of Immunology
spellingShingle Bezerra, Caroline A., Cardoso, Thiago M., Giudice, Angela, Porto, Aurélia F., Santos, Silvane B., Carvalho, Edgar M., Bacellar, Olívia, Scandinavian Journal of Immunology, Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals, Immunology, General Medicine
title Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_full Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_fullStr Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_full_unstemmed Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_short Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
title_sort evaluation of the microbicidal activity and cytokines/chemokines profile released by neutrophils from htlv‐1‐infected individuals
title_unstemmed Evaluation of the Microbicidal Activity and Cytokines/Chemokines Profile Released by Neutrophils from HTLV‐1‐Infected Individuals
topic Immunology, General Medicine
url http://dx.doi.org/10.1111/j.1365-3083.2011.02579.x