Journal
AIDS
Volume 21, Issue 18, Pages 2399-2408Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/QAD.0b013e3282f25107
Keywords
AIDS; bacteria; cytokines; human; monocytes/macrophages
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Funding
- Wellcome Trust Funding Source: Medline
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Background: Adults with advanced HIV are susceptible to invasive and recrudescent infections with nontyphoidal salmonellae. Objectives: To examine whether persistence and recurrence of salmonella infection results from HIV-related defects in macrophage internalization and intracellular killing or from ineffective type 1 cytokine responses. Such defects could be a direct consequence of macrophage HIV infection or secondary to reduced enhancement of macrophage effector functions by interferon-gamma (IFN gamma) as CD4 cell count falls. Design: Ex-vivo scientific case-control study. Methods: Primary ex-vivo human alveolar macrophages (huAM) from HIV-negative and HIV-positive subjects were challenged with Salmonella typhimurium under unprimed and IFN gamma-primed conditions to study internalization and intracellular killing of bacteria and cytokine responses of huAM. Results: Priming of huAM with IFN gamma reduced bacterial internalization but enhanced microbicidal activity against intracellular salmonellae. HuAM from HIV-positive subjects showed unimpaired internalization and intracellular killing of salmonellae, with and without IFN gamma priming. Opsonic and mannose receptor (CD206)-mediated entry was not required for optimal internalization. HuAM from HIV-positive subjects, however, exhibited increased secretion of tumour necrosis factor a (TNF alpha), interleukin (IL)-10 and IL-12 in response to S. typhimurium challenge, regardless of IFN gamma priming. This cytokine dysregulation showed a trend to a curvilinear relationship with peripheral CD4 cell count, with marked decline at values < 250cell/mu l. Conclusions: Dysregulation of proinflammatory cytokine release, including IL-12, by macrophages during salmonella infection may underlie the susceptibility to severe salmonellosis in patients with AIDS. This defect was not reversed by IFN gamma and may represent a proinflammatory effect of HIV infection upon the macrophage or the alveolar milieu. 2007 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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