(Q44997831)

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TLR ligands and antigen need to be coencapsulated into the same biodegradable microsphere for the generation of potent cytotoxic T lymphocyte responses

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Europe PubMed Central

PubMed publication ID

8 December 2017

TLR ligands and antigen need to be coencapsulated into the same biodegradable microsphere for the generation of potent cytotoxic T lymphocyte responses (English)

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Europe PubMed Central

PubMed publication ID

8 December 2017

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toll-like receptor

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1 reference

based on heuristic

inferred from title

biodegradable microsphere

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based on heuristic

inferred from title

Marcus Groettrup

7

object named as

Marcus Groettrup

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author name string

Eva Schlosser

1

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Europe PubMed Central

PubMed publication ID

8 December 2017

Marc Mueller

2

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Europe PubMed Central

PubMed publication ID

8 December 2017

Stefan Fischer

3

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Europe PubMed Central

PubMed publication ID

8 December 2017

Sameh Basta

4

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Europe PubMed Central

PubMed publication ID

8 December 2017

Dirk H Busch

5

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Europe PubMed Central

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8 December 2017

Bruno Gander

6

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8 December 2017

language of work or name

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publication date

6 February 2008

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Europe PubMed Central

PubMed publication ID

8 December 2017

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Europe PubMed Central

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8 December 2017

26

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Europe PubMed Central

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8 December 2017

13

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Europe PubMed Central

PubMed publication ID

8 December 2017

1626-1637

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Europe PubMed Central

PubMed publication ID

8 December 2017

Tolerogenic dendritic cells

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Immunostimulatory DNA-based vaccines induce cytotoxic lymphocyte activity by a T-helper cell-independent mechanism

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Protective CD8 T cell immunity triggered by CpG-protein conjugates competes with the efficacy of live vaccines

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Antigenic Epitopes Fused to Cationic Peptide Bound to Oligonucleotides Facilitate Toll-Like Receptor 9-Dependent, but CD4+ T Cell Help-Independent, Priming of CD8+ T Cells

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Nonmethylated CG motifs packaged into virus-like particles induce protective cytotoxic T cell responses in the absence of systemic side effects

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Hydrophilic poly(DL-lactide-co-glycolide) microspheres for the delivery of DNA to human-derived macrophages and dendritic cells

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MHC class I- and class II-restricted processing and presentation of microencapsulated antigens.

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ER-phagosome fusion defines an MHC class I cross-presentation compartment in dendritic cells

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Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens

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10.1016/J.VACCINE.2008.01.030

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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