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Infection and Immunity, January 2001, p. 288-296, Vol. 69, No. 1
Department of Immunology, Istituto Superiore
di Sanità,1 Institute of
Biomedical Technology, CNR,4 and
Department of Infectious and Tropical Diseases, University of
Rome "La Sapienza",5 Rome, and
Department of Experimental Pathology,
B.M.I.E.,2 and Department of Oncology,
Hematology Division, University of Pisa,3 Pisa,
Italy
Received 24 July 2000/Returned for modification 31 August
2000/Accepted 4 October 2000
By directly suppressing the function of certain immune cell subsets
and by stimulating other cell populations related to immunopathology, parasite-derived substances play an important role in the chronic establishment of parasitic disease. Our objective was twofold: (i) to
investigate further the role of Echinococcus granulosus antigen B (AgB) in the human early inflammatory response by determining its effect on polymorphonuclear cell (PMN) random migration,
chemotaxis, and oxidative metabolism and (ii) to determine its action
in acquired immunity by evaluating AgB and sheep hydatid fluid
(SHF)-driven Th1 (gamma interferon [IFN-
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.1.288-296.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Modulation of Human Immune Response by Echinococcus
granulosus Antigen B and Its Possible Role in Evading Host
Defenses
] and
interleukin 12 [IL-12]) and Th2 (IL-4 and IL-13) cytokine
production by peripheral blood mononuclear cells (PBMC) from 40 patients who had cured or stable or progressive cystic echinococcosis.
AgB significantly inhibited PMN recruitment but left their random
migration and oxidative metabolism unchanged. Patients' PBMC
stimulated with AgB produced IL-4 and IL-13 but did not produce IL-12.
They also produced significantly lower IFN-
concentrations than did
PBMC stimulated with SHF (P = 10
5). AgB
skewed the Th1/Th2 cytokine ratios towards a preferentially immunopathology-associated Th2 polarization, predominantly in patients
with progressive disease. AgB-stimulated patients' PBMC also
proliferated less than SHF-stimulated PBMC (P = 9 × 10
3). In vitro Th2 cytokine production was reflected
in vivo by elevated specific immunoglobulin E (IgE) and IgG4 antibodies
binding to AgB. These findings confirm that AgB plays a role in the
escape from early immunity by inhibiting PMN chemotaxis. They also
add new information on the host-parasite relationship, suggesting that
AgB exploits the activation of T helper cells by eliciting a
nonprotective Th2 cell response.
*
Corresponding author. Mailing address: Department of
Immunology, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy. Phone: 39.06.49902760. Fax: 39.06.49387115. E-mail: siracusano{at}iss.it.
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