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Infection and Immunity, March 1999, p. 1338-1346, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Potent Immunoregulatory Effects of Salmonella
typhi Flagella on Antigenic Stimulation of Human Peripheral Blood
Mononuclear Cells
Timothy L.
Wyant,
Michael K.
Tanner, and
Marcelo B.
Sztein*
Center for Vaccine Development, Departments
of Pediatrics and Medicine, University of Maryland, Baltimore,
Maryland 21201
Received 22 July 1998/Returned for modification 5 October
1998/Accepted 30 November 1998
A key function of monocytes/macrophages (M
) is to present
antigens to T cells. However, upon interaction with bacteria, M
lose
their ability to effectively present soluble antigens. This functional
loss was associated with alterations in the expression of adhesion
molecules and CD14 and a reduction in the uptake of soluble antigen.
Recently, we have demonstrated that Salmonella typhi
flagella (STF) markedly decrease CD14 expression and are potent
inducers of proinflammatory cytokine production by human peripheral
blood mononuclear cells (hPBMC). In order to determine whether S. typhi and soluble STF also alter the ability of M
to activate
T cells to proliferate to antigens and mitogens, hPBMC were cultured in
the presence of tetanus toxoid (TT) or phytohemagglutinin (PHA) and
either killed whole-cell S. typhi or purified STF protein. Both whole-cell S. typhi and STF suppressed
proliferation to PHA and TT. This decreased proliferation was not a
result of increased M
production of nitric oxide, prostaglandin
E2, or oxygen radicals or the release of interleukin-1
,
tumor necrosis factor alpha, interleukin-6, or interleukin-10 following
exposure to STF. However, the ability to take up soluble antigen, as
determined by fluorescein isothiocyanate-labeled dextran uptake, was
reduced in cells cultured with STF. Moreover, there was a dramatic
reduction in the expression of CD54 on M
after exposure to STF.
These results indicate that whole-cell S. typhi and STF
have the ability to alter in vitro proliferation to soluble antigens
and mitogens by affecting M
function.
*
Corresponding author. Mailing address: Center for
Vaccine Development, Department of Pediatrics, University of Maryland,
685 W. Baltimore St., Rm. 480, Baltimore, MD 21201. Phone: (410)
706-5328. Fax: (410) 706-6205. E-mail:
msztein{at}UMPPA1.ab.umd.edu.
Infection and Immunity, March 1999, p. 1338-1346, Vol. 67, No. 3
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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