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Journal of Virology, April 2001, p. 3164-3174, Vol. 75, No. 7
Centro de Investigación en Sanidad
Animal, INIA, Valdeolmos, 28130 Madrid,1
Centro de Biología Molecular "Severo Ochoa"
(CSIC-UAM), Cantoblanco, 28049 Madrid,2
and Departament de Química Orgànica,
Universitat de Barcelona, 08028 Barcelona,3
Spain
Received 3 July 2000/Accepted 27 December 2000
Porcine T-cell recognition of foot-and-mouth disease virus (FMDV)
nonstructural proteins (NSP) was tested using in vitro
lymphoproliferative responses. Lymphocytes were obtained from outbred
pigs experimentally infected with FMDV. Of the different NSP,
polypeptides 3A, 3B, and 3C gave the highest stimulations in the
in vitro assays. The use of overlapping synthetic peptides allowed the
identification of amino acid regions within these proteins
that were efficiently recognized by the lymphocytes. The sequences of
some of these antigenic peptides were highly conserved among different
FMDV serotypes. They elicited major histocompatibility
complex-restricted responses with lymphocytes from pigs infected
with either a type C virus or reinfected with a
heterologous FMDV. A tandem peptide containing the T-cell peptide
3A[21-35] and the B-cell antigenic site VP1[137-156] also
efficiently stimulated lymphocytes from infected animals in vitro.
Furthermore, this tandem peptide elicited significant
levels of serotype-specific antiviral activity, a result consistent
with the induction of anti-FMDV antibodies. Thus,
inclusion in the peptide formulation of a T-cell epitope derived
from the NSP 3A possessing the capacity to induce T helper activity can allow cooperative induction of anti-FMDV antibodies by B cells.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.7.3164-3174.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Identification of T-Cell Epitopes in Nonstructural
Proteins of Foot-and-Mouth Disease Virus
*
Corresponding author. Mailing address: CBMSO,
Cantoblanco 28049, Madrid, Spain. Phone: 34-91-6202300. Fax:
34-91-6202247. E-mail: fsobrino{at}cnb.uam.es.
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