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Infection and Immunity, April 2000, p. 1879-1883, Vol. 68, No. 4
Laboratory of Immunology, Istituto
Dermopatico dell'Immacolata, IRCCS, Rome,1 and
Section of Microbiology, Department of Molecular Biology,
University of Siena,2 Italy
Received 18 November 1999/Returned for modification 17 December
1999/Accepted 3 January 2000
Bacteria are being actively investigated as vaccine carriers for
inducing or boosting protective immune responses. In this study, human
monocyte-derived dendritic cells (DCs) and normal B cells were compared
for their capacity to present the C fragment of tetanus toxin (TTFC),
expressed on the surface of recombinant Streptococcus
gordonii, to specific CD4+ T lymphocytes. DCs were
more efficient than B cells at presenting soluble TTFC and remarkably
more capable of presenting bacterium-associated TTFC both in terms of
the amount of antigen required to obtain a given T-cell response and on
a per-cell basis. This difference was associated with a much lower
capacity of B cells to endocytose soluble TTFC and phagocytose
recombinant S. gordonii. In addition, S. gordonii induced the phenotypic maturation of DCs but not of B
cells. The results thus indicate that DCs but not B cells play a
crucial role in the amplification of class II-restricted immune responses induced by immunization with recombinant gram-positive bacteria.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Human Dendritic Cells Are Superior to B Cells at
Presenting a Major Histocompatibility Complex Class II-Restricted
Heterologous Antigen Expressed on Recombinant Streptococcus
gordonii
*
Corresponding author. Mailing address: Laboratory of
Immunology, Istituto Dermopatico dell'Immacolata, IRCCS. Via dei Monti di Creta 104, 00167 Rome, Italy. Phone: 39-06-6646-4718. Fax: 39-06-6646-4705. E-mail: imm1{at}idi.it.
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