Evaluation of yellow fever virus 17D strain as a new vector for HIV-1 vaccine development (Q39684793)

14 September 2017

Evaluation of yellow fever virus 17D strain as a new vector for HIV-1 vaccine development (English)

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14 September 2017

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6

Charles M Rice

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14 September 2017

David Franco

1

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14 September 2017

Wenjing Li

2

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14 September 2017

Fang Qing

3

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14 September 2017

Cristina T Stoyanov

4

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14 September 2017

Thomas Moran

5

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14 September 2017

David D Ho

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14 September 2017

language of work or name

English

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publication date

29 June 2010

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28

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35

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14 September 2017

5676-5685

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The spread, treatment, and prevention of HIV-1: evolution of a global pandemic

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HIV-1 vaccine-induced immunity in the test-of-concept Step Study: a case-cohort analysis

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Human cytotoxic T lymphocyte responses to live attenuated 17D yellow fever vaccine: identification of HLA-B35-restricted CTL epitopes on nonstructural proteins NS1, NS2b, NS3, and the structural protein E.

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Yellow fever vaccine YF-17D activates multiple dendritic cell subsets via TLR2, 7, 8, and 9 to stimulate polyvalent immunity

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Cutaneous delivery of a live, attenuated chimeric flavivirus vaccine against Japanese encephalitis (ChimeriVax)-JE) in non-human primates.

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A recombinant Yellow Fever 17D vaccine expressing Lassa virus glycoproteins

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Recombinant Yellow Fever Vaccine Virus 17D Expressing Simian Immunodeficiency Virus SIVmac239 Gag Induces SIV-Specific CD8+ T-Cell Responses in Rhesus Macaques

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

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Evaluation of an Indirect Immunofluorescence Assay for Detection of Immunoglobulin M (IgM) and IgG Antibodies against Yellow Fever Virus

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Construction and characterization of recombinant flaviviruses bearing insertions between E and NS1 genes

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Fine Mapping of a cis-Acting Sequence Element in Yellow Fever Virus RNA That Is Required for RNA Replication and Cyclization

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Conserved elements in the 3' untranslated region of flavivirus RNAs and potential cyclization sequences

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Essential role of cyclization sequences in flavivirus RNA replication

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Protective effects of a live attenuated SIV vaccine with a deletion in the nef gene

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Neurovirulence of yellow fever 17DD vaccine virus to rhesus monkeys

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Human effector and memory CD8+ T cell responses to smallpox and yellow fever vaccines

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Surface expression of an immunodominant malaria protein B cell epitope by yellow fever virus

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Yellow fever 17D as a vaccine vector for microbial CTL epitopes

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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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Recombinant yellow fever viruses are effective therapeutic vaccines for treatment of murine experimental solid tumors and pulmonary metastases

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Current Assessment of Yellow Fever and Yellow Fever Vaccine

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Yellow fever vaccine induces integrated multilineage and polyfunctional immune responses

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Systems biology approach predicts immunogenicity of the yellow fever vaccine in humans

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CD8+ T-cell responses to different HIV proteins have discordant associations with viral load

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Comprehensive analysis of human immunodeficiency virus type 1-specific CD4 responses reveals marked immunodominance of gag and nef and the presence of broadly recognized peptides

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Comprehensive epitope analysis of human immunodeficiency virus type 1 (HIV-1)-specific T-cell responses directed against the entire expressed HIV-1 genome demonstrate broadly directed responses, but no correlation to viral load.

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Analysis of total human immunodeficiency virus (HIV)-specific CD4(+) and CD8(+) T-cell responses: relationship to viral load in untreated HIV infection

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Hierarchical targeting of subtype C human immunodeficiency virus type 1 proteins by CD8+ T cells: correlation with viral load

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Broad and Gag-biased HIV-1 epitope repertoires are associated with lower viral loads

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Multifunctional TH1 cells define a correlate of vaccine-mediated protection against Leishmania major

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Mutagenesis of the NS2B-NS3-mediated cleavage site in the flavivirus capsid protein demonstrates a requirement for coordinated processing

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inferred from DOI database lookup

7 January 2021

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DOI

10.1016/J.VACCINE.2010.06.052

1 reference

14 September 2017

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