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Infect. Immun., 11 1997, 4483-4487, Vol 65, No. 11
NM Ampel and L Christian
Using peripheral blood mononuclear cells (PBMC) from individuals with or
without coccidioidal delayed-type hypersensitivity (DTH), we examined and
attempted to modulate the in vitro responses of PBMC from various donors to
the coccidioidal antigen toluene spherule lysate (TSL). Among healthy
DTH-positive donors, 100 ng of human recombinant interleukin-10 (IL-10) per
ml suppressed both PBMC proliferation (P = 0.01) and gamma interferon
(IFN-gamma) and IL-12 production (for both, P < 0.05). In vitro
proliferation and production of IFN-gamma and IL-12 by PBMC were
significantly higher in DTH-positive donors with active coccidioidomycosis
than in healthy, nonimmune controls (P < 0.05) but not in active
DTH-negative donors with or without human immunodeficiency virus infection
(for both, P > 0.05). Human recombinant IL-12 increased IFN-gamma
production by PBMC from active, DTH-positive donors (P = 0.01) but not by
PBMC from DTH-negative groups. For healthy DTH-positive donors, the median
antigen-reactive cell frequency per 10(5) PBMC was 3.7, compared to 1.7 in
DTH-negative donors with active coccidioidomycosis (P = 0.03). These data
indicate that the in vitro TSL response is highly dependent on coccidioidal
DTH. Not only do PBMC from individuals with DTH appear to respond to TSL,
but their response can be modulated in vitro with either IL-10 or IL- 12.
On the other hand, PBMC from DTH-negative individuals do not respond in
vitro to TSL and their response is not modulable, suggesting a lack of
antigen response.
Copyright © 1997, American Society for Microbiology
In vitro modulation of proliferation and cytokine production by human peripheral blood mononuclear cells from subjects with various forms of coccidioidomycosis
Department of Medicine, University of Arizona College of Medicine, Tucson Veterans Affairs Medical Center, 85723, USA. nampel@u.arizona.edu
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