2000
DOI: 10.1016/s0264-410x(00)00313-3
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Association of bovine DRB3 alleles with immune response to FMDV peptides and protection against viral challenge

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Cited by 53 publications
(46 citation statements)
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“…In particular, the amino acid residues 70-71 of the OLA-DRβ1 domain from peptide-binding pocket 4 might be the most important sites in immune responses. Likewise, several previous studies revealed a strong association between BoLA-DRB3 and sensitivity to subclinical progression of BLV (48) and BLV-induced lymphoma (1) as well as immune response by peptide vaccine against Foot-andMouth disease virus (FMDV) (12). Furthermore, Haghparast et al (15) reported that the affinity of the FMDV epitope peptides to bind to certain BoLA-DRB3 molecules was significantly correlated with the capacity to induce T-cell proliferation.…”
Section: Discussionmentioning
confidence: 92%
“…In particular, the amino acid residues 70-71 of the OLA-DRβ1 domain from peptide-binding pocket 4 might be the most important sites in immune responses. Likewise, several previous studies revealed a strong association between BoLA-DRB3 and sensitivity to subclinical progression of BLV (48) and BLV-induced lymphoma (1) as well as immune response by peptide vaccine against Foot-andMouth disease virus (FMDV) (12). Furthermore, Haghparast et al (15) reported that the affinity of the FMDV epitope peptides to bind to certain BoLA-DRB3 molecules was significantly correlated with the capacity to induce T-cell proliferation.…”
Section: Discussionmentioning
confidence: 92%
“…In addition, two tandem peptides containing the sequence of the continuous B-cell epitope VP1 [137][138][139][140][141][142][143][144][145][146][147][148][149][150][151][152][153][154][155][156] juxtaposed to the T-cell epitope 3A [21][22][23][24][25][26][27][28][29][30][31][32][33][34][35], in the two possible orientations (peptides BT and TB; Table 1), were prepared. Both peptides were synthesized as C-terminal carboxamides by Boc-based solid-phase methods (12) in semiautomated mode, with systematic ninhydrin control and recoupling as required.…”
Section: Methodsmentioning
confidence: 99%
“…Inclusion of one of these T-cell epitopes identified in VP1 residues 21 to 40 in a tandem peptide with the B-cell site A has been shown to overcome individual nonresponsiveness of cattle to peptide A (17). However, the recognition of this and other T-cell epitopes identified in FMDV capsid proteins is significantly restricted by the MHC polymorphism of the host species (24,26,39), and their potential to improve synthetic vaccines is, therefore, limited. Yet T-cell epitopes relevant to the induction of a protective response have also been described in the NSP of several viruses (13,27).…”
mentioning
confidence: 99%
“…Such T cell peptides should ideally be recognised by T lymphocytes in the context of alleles of MHC class II frequently represented in the populations of the natural hosts [194]. Even when G-H loop peptides can stimulate T cells of individuals from host species [105,189,232,252], this recognition seems to be considerably restricted by the individual MHC composition [101,[104][105][106]239], and may vary depending on the sequence of the viral peptide used [105]. Immunisation with peptides including the G-H loop either alone or in combination with an independent T cell epitope has been reported recently [232], using a large number of cattle.…”
Section: Peptide Vaccinesmentioning
confidence: 99%