(Q52009810)

19 April 2018

title

Optimization of DNA vaccination against cutaneous leishmaniasis. (English)

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19 April 2018

author

Yasmine Belkaid

2

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19 April 2018

author name string

Susana Méndez

1

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19 April 2018

Robert A Seder

3

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19 April 2018

David Sacks

4

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19 April 2018

language of work or name

English

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publication date

1 November 2002

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19 April 2018

published in

Vaccine

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19 April 2018

volume

20

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19 April 2018

issue

31-32

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19 April 2018

page(s)

3702-3708

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19 April 2018

DNA vaccines: a key for inducing long-term cellular immunity

cites work

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Vaccination with plasmid DNA encoding TSA/LmSTI1 leishmanial fusion proteins confers protection against Leishmania major infection in susceptible BALB/c mice

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7 January 2021

The potency and durability of DNA- and protein-based vaccines against Leishmania major evaluated using low-dose, intradermal challenge.

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CD8+ T cells are required for primary immunity in C57BL/6 mice following low-dose, intradermal challenge with Leishmania major.

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Requirements for the maintenance of Th1 immunity in vivo following DNA vaccination: a potential immunoregulatory role for CD8+ T cells

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The role of antigen and IL-12 in sustaining Th1 memory cells in vivo: IL-12 is required to maintain memory/effector Th1 cells sufficient to mediate protection to an infectious parasite challenge

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Development of a natural model of cutaneous leishmaniasis: powerful effects of vector saliva and saliva preexposure on the long-term outcome of Leishmania major infection in the mouse ear dermis

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Genetic vaccination against leishmaniasis

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Genetic immunization with glycoprotein 63 cDNA results in a helper T cell type 1 immune response and protection in a murine model of leishmaniasis

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Vaccination with DNA encoding the immunodominant LACK parasite antigen confers protective immunity to mice infected with Leishmania major

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A protective cocktail vaccine against murine cutaneous leishmaniasis with DNA encoding cysteine proteinases of Leishmania major

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A natural model of Leishmania major infection reveals a prolonged "silent" phase of parasite amplification in the skin before the onset of lesion formation and immunity.

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Leishmania donovani p36(LACK) DNA vaccine is highly immunogenic but not protective against experimental visceral leishmaniasis

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Protection against cutaneous leishmaniasis induced by recombinant antigens in murine and nonhuman primate models of the human disease

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Gene inoculation generates immune responses against human immunodeficiency virus type 1

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Direct gene transfer in skeletal muscle: plasmid DNA-based immunization against the hepatitis B virus surface antigen

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Mucosal immunization with a DNA vaccine induces immune responses against HIV-1 at a mucosal site

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Safety and immunogenicity of intramuscular and intravaginal delivery of HIV-1 DNA constructs to infant chimpanzees.

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Immunity to Plasmodium falciparum malaria sporozoites by somatic transgene immunization

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7 January 2021

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7 January 2021

The immunobiology of muscle

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7 January 2021

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A heterologous prime-boost regime using DNA and recombinant vaccinia virus expressing the Leishmania infantum P36/LACK antigen protects BALB/c mice from cutaneous leishmaniasis.

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7 January 2021

Enhanced CD8 T cell immunogenicity and protective efficacy in a mouse malaria model using a recombinant adenoviral vaccine in heterologous prime-boost immunisation regimes

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Identifiers

DOI

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19 April 2018

1 reference

19 April 2018