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Infection and Immunity, September 2001, p. 5305-5312, Vol. 69, No. 9
Department of Biochemistry and Immunology,
School of Medicine of Ribeirão Preto,1 and
School of Pharmacy of Ribeirão
Preto,2 University of São Paulo,
Ribeirão Preto, SP, and Faculty of Pharmacy, Federal
University of Minas Gerais, Belo Horizonte, MG,3
Brazil
Received 18 September 2000/Returned for modification 4 December
2000/Accepted 29 May 2001
Mice treated with viable Mycobacterium
tuberculosis with no glycolipid trehalose dimycolate
(TDM) on the outer cell wall (delipidated M. tuberculosis)
by intraperitoneal or intratracheal inoculation presented an intense
recruitment of polymorphonuclear cells into the peritoneal cavity and
an acute inflammatory reaction in the lungs, respectively. In addition,
lung lesions were resolved around the 32nd day after intratracheal
inoculation. TDM-loaded biodegradable poly-DL-lactide-coglycolide microspheres as well as
TDM-coated charcoal particles induced an intense inflammatory
reaction. In addition, high levels of interleukin-6 (IL-6), tumor
necrosis factor alpha (TNF-
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.9.5305-5312.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Role of Trehalose Dimycolate in Recruitment of Cells
and Modulation of Production of Cytokines and NO in
Tuberculosis
), IL-12, IL-10, gamma
interferon (IFN-
), and IL-4 production were detected in lung cells,
and nitric oxide (NO) production was high in culture supernatants of
bronchoalveolar lavage cells. These in vivo data were confirmed
by in vitro experiments using peritoneal macrophages cultured in the
presence of TDM adsorbed onto coverslips. High levels of
IFN-
, IL-6, TNF-
, IL-12, IL-10, and NO were detected in the
culture supernatants. Our results suggest that TDM contributes to
persistence of infection through production of cytokines,
which are important for the recruitment of inflammatory cells and
maintenance of a granulomatous reaction. In addition, our
findings are important for a better understanding of the
immunostimulatory activity of TDM and its possible use as an
adjuvant in experiments using DNA vaccine or gene therapy against tuberculosis.
*
Corresponding author. Mailing address: Department of
Biochemistry and Immunology, School of Medicine of Ribeirão
Preto, University of São Paulo, 14049-900 Ribeirão Preto,
SP, Brazil. Phone: 55 16 602 3228. Fax: 55 16 633 6840. E-mail:
clsilya{at}fmrp.usp.br.
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