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dc.contributor.authorTan, D.
dc.contributor.authorYong, Y.
dc.contributor.authorLim, A.
dc.contributor.authorTan, H.
dc.contributor.authorKamarulzaman, A.
dc.contributor.authorFrench, M.
dc.contributor.authorPrice, Patricia
dc.date.accessioned2017-01-30T12:51:13Z
dc.date.available2017-01-30T12:51:13Z
dc.date.created2015-10-29T04:10:07Z
dc.date.issued2011
dc.identifier.citationTan, D. and Yong, Y. and Lim, A. and Tan, H. and Kamarulzaman, A. and French, M. and Price, P. 2011. Robust interferon-a and IL-12 responses by dendritic cells are related to efficient CD4+ T-cell recovery in HIV patients on ART. Clinical Immunology. 139 (2): pp. 115-121.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/25996
dc.identifier.doi10.1016/j.clim.2011.02.015
dc.description.abstract

Amongst HIV patients with successful virological responses to antiretroviral therapy (ART), poor CD4+ T-cell recovery is associated with low nadir CD4+ T-cell counts and persistent immune activation. These factors might be influenced by dendritic cell (DC) function. Interferon-a-producing plasmacytoid DC and IL-12-producing myeloid DC were quantified by flow cytometry after stimulation with agonists to TLR7/8 (CL075) or TLR9 (CpG-ODN). These were compared between patients who achieved CD4+ T-cell counts above or below 200 cells/µL after 6months on ART (High vs. Low groups). High Group patients had more DC producing interferon-a or IL-12 at Weeks 6 and 12 on ART than Low Group patients. The frequencies of cytokine-producing DC at Week 12 were directly correlated with CD4+ T-cell counts at baseline and at Week 12. Patients with good recovery of CD4+ T-cells had robust TLR-mediated interferon-a responses by plasmacytoid DC and IL-12 responses by myeloid DC during early ART (1-3months). © 2011 Elsevier Inc.

dc.titleRobust interferon-a and IL-12 responses by dendritic cells are related to efficient CD4+ T-cell recovery in HIV patients on ART
dc.typeJournal Article
dcterms.source.volume139
dcterms.source.number2
dcterms.source.startPage115
dcterms.source.endPage121
dcterms.source.issn1521-6616
dcterms.source.titleClinical Immunology
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available


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