Immunization with chaperone-peptide complex induces low-avidity cytotoxic T lymphocytes providing transient protection against herpes simplex virus infection (Q34326744)

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English	Immunization with chaperone-peptide complex induces low-avidity cytotoxic T lymphocytes providing transient protection against herpes simplex virus infection	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Immunization with chaperone-peptide complex induces low-avidity cytotoxic T lymphocytes providing transient protection against herpes simplex virus infection (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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molecular chaperones

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Małgorzata Gieryńska

2

object named as

Malgorzata Gierynska

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Udayasankar Kumaraguru

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Shanna Norman

3

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Europe PubMed Central

PubMed publication ID

1 August 2017

Barry D Bruce

4

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Europe PubMed Central

PubMed publication ID

1 August 2017

Barry T Rouse

5

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Europe PubMed Central

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1 August 2017

language of work or name

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publication date

1 January 2002

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Europe PubMed Central

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1 August 2017

Journal of Virology

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Europe PubMed Central

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1 August 2017

76

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Europe PubMed Central

PubMed publication ID

1 August 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

136-141

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Europe PubMed Central

PubMed publication ID

1 August 2017

HSP70 peptidembearing and peptide-negative preparations act as chaperokines

1 reference

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High-avidity CTL exploit two complementary mechanisms to provide better protection against viral infection than low-avidity CTL.

1 reference

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Receptor-mediated uptake of antigen/heat shock protein complexes results in major histocompatibility complex class I antigen presentation via two distinct processing pathways

1 reference

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6 July 2018

Application of the intracellular gamma interferon assay to recalculate the potency of CD8( ) T-cell responses to herpes simplex virus

1 reference

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6 July 2018

Induction of cellular immunity by immunization with novel hybrid peptides complexed to heat shock protein 70

1 reference

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In vivo cytotoxic T lymphocyte elicitation by mycobacterial heat shock protein 70 fusion proteins maps to a discrete domain and is CD4( ) T cell independent

1 reference

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Advances in vaccine adjuvants

1 reference

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The cytotoxic T-cell response to herpes simplex virus type 1 infection of C57BL/6 mice is almost entirely directed against a single immunodominant determinant.

1 reference

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Viral immune evasion due to persistence of activated T cells without effector function

1 reference

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Immunization with a single major histocompatibility complex class I-restricted cytotoxic T-lymphocyte recognition epitope of herpes simplex virus type 2 confers protective immunity.

1 reference

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Immunization with a lymphocytic choriomeningitis virus peptide mixed with heat shock protein 70 results in protective antiviral immunity and specific cytotoxic T lymphocytes

1 reference

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Heat shock fusion proteins as vehicles for antigen delivery into the major histocompatibility complex class I presentation pathway

1 reference

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6 July 2018

Heat Shock Protein–Peptide Complexes, Reconstituted In Vitro, Elicit Peptide-specific Cytotoxic T Lymphocyte Response and Tumor Immunity

1 reference

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6 July 2018

Heat shock protein 70-associated peptides elicit specific cancer immunity

1 reference

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6 July 2018

Tumor rejection antigen gp96/grp94 is an ATPase: implications for protein folding and antigen presentation

1 reference

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6 July 2018

Cellular requirements for tumor-specific immunity elicited by heat shock proteins: tumor rejection antigen gp96 primes CD8 T cells in vivo

1 reference

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Vaccine technologies: view to the future

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6 July 2018

Roles of different T-cell subsets in control of herpes simplex virus infection determined by using T-cell-deficient mouse-models.

1 reference

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Discrepancy between in vitro measurable and in vivo virus neutralizing cytotoxic T cell reactivities. Low T cell receptor specificity and avidity sufficient for in vitro proliferation or cytotoxicity to peptide-coated target cells but not for in viv

1 reference

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Two intermediate-avidity cytotoxic T lymphocyte clones with a disparity between functional avidity and MHC tetramer staining

1 reference

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27 October 2018

Lymphotoxin alpha-/- mice develop functionally impaired CD8 T cell responses and fail to contain virus infection of the central nervous system

1 reference

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Generation of tumor-specific cytotoxic T lymphocytes and memory T cells by immunization with tumor-derived heat shock protein gp96.

1 reference

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Synthetic peptides non-covalently bound to bacterial hsp 70 elicit peptide-specific T-cell responses in vivo

1 reference

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27 October 2018

HSP70 stimulates cytokine production through a CD14-dependant pathway, demonstrating its dual role as a chaperone and cytokine

1 reference

https://pubmed.ncbi.nlm.nih.gov/11739679

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitation of CD8( ) T-lymphocyte responses to multiple epitopes from simian virus 40 (SV40) large T antigen in C57BL/6 mice immunized with SV40, SV40 T-antigen-transformed cells, or vaccinia virus recombinants expressing full-length T antigen or

1 reference

https://pubmed.ncbi.nlm.nih.gov/11739679

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mechanism for the specific immunogenicity of heat shock protein-chaperoned peptides

1 reference

https://pubmed.ncbi.nlm.nih.gov/11739679

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CD4-independent in vivo priming of murine CTL by optimal MHC class I-restricted peptides derived from intracellular pathogens

1 reference

https://pubmed.ncbi.nlm.nih.gov/11739679

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adjuvant-free hsp70 fusion protein system elicits humoral and cellular immune responses to HIV-1 p24

1 reference

https://pubmed.ncbi.nlm.nih.gov/11739679

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/JVI.76.1.136-141.2002

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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