Comprehensive analysis of T cell epitope discovery strategies using 17DD yellow fever virus structural proteins and BALB/c (H2d) mice model (Q27487555)

4

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Ernesto T A Marques

8

object named as

Ernesto T A Marques

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John Sidney

5

object named as

John Sidney

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author name string

Milton Maciel

1

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Srinivasan N Kellathur

2

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Pryia Chikhlikar

3

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Thomas J August

From functional genomics to functional immunomics: new challenges, old problems, big rewards

7

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language of work or name

English

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publication date

15 August 2008

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published in

Virology

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volume

378

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issue

1

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page(s)

105-17

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cites work

1 reference

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Live attenuated yellow fever 17D infects human DCs and allows for presentation of endogenous and recombinant T cell epitopes

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PREDBALB/c: a system for the prediction of peptide binding to H2d molecules, a haplotype of the BALB/c mouse.

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Mapping T cell epitopes by flow cytometry

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Antiviral cytotoxic T cells cross-reactively recognize disparate peptide determinants from related viruses but ignore more similar self- and foreign determinants

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Comparison of the nucleotide and deduced amino acid sequences of the structural protein genes of the yellow fever 17DD vaccine strain from Senegal with those of other yellow fever vaccine viruses

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Complete nucleotide sequence of yellow fever virus vaccine strains 17DD and 17D-213.

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CD4 T cells guarantee optimal competitive fitness of CD8 memory T cells

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The ability of peptides to induce cytotoxic T cells in vitro does not strongly correlate with their affinity for the H-2Ld molecule: implications for vaccine design and immunotherapy

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