Immunization with a single major histocompatibility complex class I-restricted cytotoxic T-lymphocyte recognition epitope of herpes simplex virus type 2 confers protective immunity. (Q33785966)

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

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6 December 2019

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

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6 December 2019

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J E Blaney

1

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6 December 2019

E Nobusawa

2

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6 December 2019

M A Brehm

3

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6 December 2019

R H Bonneau

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6 December 2019

L M Mylin

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6 December 2019

T M Fu

6

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6 December 2019

Y Kawaoka

7

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6 December 2019

S S Tevethia

8

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6 December 2019

publication date

1 December 1998

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6 December 2019

Journal of Virology

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6 December 2019

72

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6 December 2019

12

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6 December 2019

9567-9574

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6 December 2019

Cytotoxic T lymphocyte escape variants, induced mutations, and synthetic peptides define a dominant H-2Kb-restricted determinant in simian virus 40 tumor antigen

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Severe genital herpes infections in HIV-infected individuals with impaired herpes simplex virus-specific CD8+ cytotoxic T lymphocyte responses

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Interferon-gamma enhances resolution of herpes simplex virus type 2 infection of the murine genital tract

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Immunization with a replication-deficient mutant of herpes simplex virus type 1 (HSV-1) induces a CD8+ cytotoxic T-lymphocyte response and confers a level of protection comparable to that of wild-type HSV-1

1 reference

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Long-lived cytotoxic T lymphocyte memory in mucosal tissues after mucosal but not systemic immunization

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High frequency of CD8+ cytotoxic T-lymphocyte precursors specific for herpes simplex viruses in persons with genital herpes

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Immunization with DNA vaccines encoding glycoprotein D or glycoprotein B, alone or in combination, induces protective immunity in animal models of herpes simplex virus-2 disease

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Epitope Specificity of H-2Kb-Restricted, HSV-1-, and HSV-2-Cross-Reactive Cytotoxic T Lymphocyte Clones

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Polymorphism within the herpes simplex virus (HSV) ribonucleotide reductase large subunit (ICP6) confers type specificity for recognition by HSV type 1-specific cytotoxic T lymphocytes

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Limiting dilution assays for the determination of immunocompetent cell frequencies. I. Data analysis.

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Cell-mediated Immunity in Herpes Simplex Virus-infected Mice: Functional Analysis of Lymph Node Cells During Periods of Acute and Latent Infection, with Reference to Cytotoxic and Memory Cells

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Cell-mediated immunity against herpes simplex induction of cytotoxic T lymphocytes

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Human cytotoxic T cell clones directed against herpes simplex virus-infected cells. II. Bifunctional clones with cytotoxic and virus-induced proliferative activities exhibit herpes simplex virus type 1 and 2 specific or type common reactivities

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Rapid and efficient site-specific mutagenesis without phenotypic selection

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Neuroinvasive properties of herpes simplex virus type 1 glycoprotein variants are controlled by the immune response.

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Mucosal immunity and protection after intranasal immunization with recombinant adenovirus expressing herpes simplex virus glycoprotein B.

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Protective vaccination against primary and recurrent disease caused by herpes simplex virus (HSV) type 2 using a genetically disabled HSV-1.

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Genetic immunization against herpes simplex virus. Protection is mediated by CD4+ T lymphocytes

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Herpes simplex virus encephalitis in a mouse model: PCR evidence for CNS latency following acute infection

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Protection of mice from fatal herpes simplex virus type 1 infection by adoptive transfer of cloned virus-specific and H-2-restricted cytotoxic T lymphocytes

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Cell-mediated Immunity in Herpes Simplex Virus-infected Mice: Induction, Characterization and Antiviral Effects of Delayed Type Hypersensitivity

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Expression of glycoprotein D of herpes simplex virus type 1 in a recombinant baculovirus: protective responses and T cell recognition of the recombinant-infected cell extracts

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Protection against lethal viral infection by vaccination with nonimmunodominant peptides

1 reference

https://pubmed.ncbi.nlm.nih.gov/9811690

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