Identification of CD4+ T cell epitopes on the fusion (F) and attachment (G) proteins of bovine respiratory syncytial virus (BRSV). (Q45737719)

15 December 2017

Identification of CD4+ T cell epitopes on the fusion (F) and attachment (G) proteins of bovine respiratory syncytial virus (BRSV). (English)

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15 December 2017

Fogg MH

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15 December 2017

Parsons KR

series ordinal

2

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15 December 2017

Thomas LH

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3

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15 December 2017

Taylor G

series ordinal

4

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15 December 2017

language of work or name

English

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publication date

1 April 2001

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15 December 2017

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15 December 2017

19

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15 December 2017

23-24

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15 December 2017

3226-3240

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Respiratory syncytial virus. Brief review

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Recombinant vaccinia viruses expressing the F, G or N, but not the M2, protein of bovine respiratory syncytial virus (BRSV) induce resistance to BRSV challenge in the calf and protect against the development of pneumonic lesions

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Nucleotide sequence analysis of the bovine respiratory syncytial virus fusion protein mRNA and expression from a recombinant vaccinia virus

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The membrane-associated and secreted forms of the respiratory syncytial virus attachment glycoprotein G are synthesized from alternative initiation codons

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Nucleotide sequence of the G protein gene of human respiratory syncytial virus reveals an unusual type of viral membrane protein

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Passive protection of gnotobiotic calves using monoclonal antibodies directed at different epitopes on the fusion protein of bovine respiratory syncytial virus

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Protection from respiratory syncytial virus infection in cotton rats by passive transfer of monoclonal antibodies

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Protective epitopes on the fusion protein of respiratory syncytial virus recognized by murine and bovine monoclonal antibodies

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Characterization of two antigenic sites recognized by neutralizing monoclonal antibodies directed against the fusion glycoprotein of human respiratory syncytial virus

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Antigenic heterogeneity of the attachment protein of bovine respiratory syncytial virus

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Antigenic structure, evolution and immunobiology of human respiratory syncytial virus attachment (G) protein

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CD4+ T cells clear virus but augment disease in mice infected with respiratory syncytial virus. Comparison with the effects of CD8+ T cells

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Distinct types of lung disease caused by functional subsets of antiviral T cells

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Enhanced pulmonary histopathology induced by respiratory syncytial virus (RSV) challenge of formalin-inactivated RSV-immunized BALB/c mice is abrogated by depletion of interleukin-4 (IL-4) and IL-10.

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Role of T-lymphocyte subsets in recovery from respiratory syncytial virus infection in calves

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Influence of selective T-lymphocyte depletion on the lung pathology of gnotobiotic calves and the distribution of different T-lymphocyte subsets following challenge with bovine respiratory syncytial virus

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Eliminating a region of respiratory syncytial virus attachment protein allows induction of protective immunity without vaccine-enhanced lung eosinophilia.

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Atypical pulmonary eosinophilia is mediated by a specific amino acid sequence of the attachment (G) protein of respiratory syncytial virus

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Immunodominant T-cell epitope on the F protein of respiratory syncytial virus recognized by human lymphocytes

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T cell epitopes of bovine respiratory syncytial virus attachment glycoprotein

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Antigenically distinct G glycoproteins of BRSV strains share a high degree of genetic homogeneity

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A comparison of three vaccines against respiratory syncytial virus in calves

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Use of synthetic peptides to identify measles nucleoprotein T-cell epitopes in vaccinated and naturally infected humans

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Recognition of a common mycobacterial T-cell epitope in MPB59 of Mycobacterium bovis.

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Universally immunogenic T cell epitopes: promiscuous binding to human MHC class II and promiscuous recognition by T cells.

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Identification of a Linear Epitope on the Fusion Glycoprotein of Respiratory Syncytial Virus

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Identification of a conserved neutralization site in the first heptad repeat of the fusion protein of respiratory syncytial virus

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A monoclonal antibody specific for a cytochrome c T cell stimulatory peptide inhibits T cell responses and affects the way the peptide associates with antigen-presenting cells

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Type II and III receptors for immunoglobulin G (IgG) control the presentation of different T cell epitopes from single IgG-complexed antigens

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Location of the epitope recognized by monoclonal antibody 63G on the primary structure of human respiratory syncytial virus G glycoprotein and the ability of synthetic peptides containing this epitope to induce neutralizing antibodies

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A subgroup-specific antigenic site in the G protein of respiratory syncytial virus forms a disulfide-bonded loop

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DOI

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15 December 2017

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