Cross-presenting dendritic cells are required for control ofLeishmania majorinfection (Q61313243)

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11 March 2020

title

Cross-presenting dendritic cells are required for control of Leishmania major infection (English)

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11 March 2020

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3

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11 March 2020

Nicolas Fasel

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Fabienne Tacchini-Cottier

11 March 2020

10

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author name string

Devika Ashok

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11 March 2020

Steffen Schuster

2

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11 March 2020

Muriel Rosa

4

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11 March 2020

Vanessa Mack

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11 March 2020

Christine Lavanchy

6

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11 March 2020

Hans Acha-Orbea

11

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11 March 2020

Silvia F Marraco

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11 March 2020

Kenneth M Murphy

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11 March 2020

language of work or name

English

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publication date

25 March 2014

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European Journal of Immunology

11 March 2020

published in

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11 March 2020

volume

44

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issue

5

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11 March 2020

page(s)

1422-1432

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The immunology of susceptibility and resistance to Leishmania major in mice

11 March 2020

cites work

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T-cell responses and immunity to experimental infection with leishmania major

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Does T Helper Differentiation Correlate with Resistance or Susceptibility to Infection with L. major? Some Insights From the Murine Model

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IL-17 promotes progression of cutaneous leishmaniasis in susceptible mice

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7 January 2021

Dendritic cells in Leishmania infection

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Dendritic cell subsets and lineages, and their functions in innate and adaptive immunity

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Neutrophil-derived CCL3 is essential for the rapid recruitment of dendritic cells to the site of Leishmania major inoculation in resistant mice

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7 January 2021

Efficient capture of infected neutrophils by dendritic cells in the skin inhibits the early anti-leishmania response

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7 January 2021

Monocyte-derived dendritic cells formed at the infection site control the induction of protective T helper 1 responses against Leishmania

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The origin and development of nonlymphoid tissue CD103+ DCs.

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Two waves of antigen-containing dendritic cells in vivo in experimental Leishmania major infection.

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Migratory dermal dendritic cells act as rapid sensors of protozoan parasites

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CD8 alpha- and Langerin-negative dendritic cells, but not Langerhans cells, act as principal antigen-presenting cells in leishmaniasis.

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Langerhans cells transport Leishmania major from the infected skin to the draining lymph node for presentation to antigen-specific T cells.

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7 January 2021

Langerhans cells are negative regulators of the anti-Leishmania response.

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7 January 2021

Lymph node resident rather than skin-derived dendritic cells initiate specific T cell responses after Leishmania major infection

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7 January 2021

MHC class II expression restricted to CD8alpha+ and CD11b+ dendritic cells is sufficient for control of Leishmania major

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7 January 2021

Hierarchy of susceptibility of dendritic cell subsets to infection by Leishmania major: inverse relationship to interleukin-12 production

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7 January 2021

The role of IL-12 in maintaining resistance to Leishmania major.

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7 January 2021

The role of IL-12 in regulation of T helper cell subsets in vivo. Lessons from experimental cutaneous leishmaniasis

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CD205 (DEC-205): a recognition receptor for apoptotic and necrotic self

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DNGR-1 is a specific and universal marker of mouse and human Batf3-dependent dendritic cells in lymphoid and nonlymphoid tissues

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7 January 2021

The CD8alpha(+) dendritic cell is responsible for inducing peripheral self-tolerance to tissue-associated antigens

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7 January 2021

Cross-presentation of viral and self antigens by skin-derived CD103+ dendritic cells

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Batf3 Deficiency Reveals a Critical Role for CD8 + Dendritic Cells in Cytotoxic T Cell Immunity

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7 January 2021

The CD8+ dendritic cell subset

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7 January 2021

CD8α(+) dendritic cells are the critical source of interleukin-12 that controls acute infection by Toxoplasma gondii tachyzoites

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7 January 2021

CD8α(+) dendritic cells are an obligate cellular entry point for productive infection by Listeria monocytogenes

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7 January 2021

Selective suicide of cross-presenting CD8+ dendritic cells by cytochrome c injection shows functional heterogeneity within this subset

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7 January 2021

IL-13 is a susceptibility factor for Leishmania major infection.

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7 January 2021

IL-17 mediates immunopathology in the absence of IL-10 following Leishmania major infection

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7 January 2021

The role of interleukin (IL)-10 in the persistence of Leishmania major in the skin after healing and the therapeutic potential of anti-IL-10 receptor antibody for sterile cure.

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7 January 2021

The Relative Contribution of IL-4 Receptor Signaling and IL-10 to Susceptibility toLeishmania major

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7 January 2021

T cell-derived IL-10 determines leishmaniasis disease outcome and is suppressed by a dendritic cell based vaccine

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7 January 2021

CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity

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7 January 2021

A role for CD103 in the retention of CD4+CD25+ Treg and control of Leishmania major infection

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7 January 2021

Compensatory dendritic cell development mediated by BATF-IRF interactions

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7 January 2021

CD8α+ DCs can be induced in the absence of transcription factors Id2, Nfil3, and Batf3.

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7 January 2021

Specificity through cooperation: BATF-IRF interactions control immune-regulatory networks

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7 January 2021

Priming of CD8+ and CD4+ T cells in experimental leishmaniasis is initiated by different dendritic cell subtypes

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Leishmania evades host immunity by inhibiting antigen cross-presentation through direct cleavage of the SNARE VAMP8.

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7 January 2021

Leishmania antigens are presented to CD8+ T cells by a transporter associated with antigen processing-independent pathway in vitro and in vivo

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7 January 2021

A limiting dilution assay for quantifying Leishmania major in tissues of infected mice

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7 January 2021

Identifiers

DOI

10.1002/EJI.201344242

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24643576%20AND%20SRC:MED&resulttype=core&format=json

11 March 2020

1 reference