IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model.
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Genetic vaccination against malaria infection by intradermal and epidermal injections of a plasmid containing the gene encoding the Plasmodium berghei circumsporozoite proteinInterferon-gamma responses to Plasmodium falciparum liver-stage antigen-1 and merozoite-surface protein-1 increase with age in children in a malaria holoendemic area of western KenyaTissue signatures influence the activation of intrahepatic CD8(+) T cells against malaria sporozoitesIn vivo CD8+ T cell dynamics in the liver of Plasmodium yoelii immunized and infected miceUpregulation of Major Histocompatibility Complex Class I on Liver Cells by Hepatitis C Virus Core Protein via p53 and TAP1 Impairs Natural Killer Cell CytotoxicityRegulation of immunopathogenesis during Plasmodium and Toxoplasma infections: more parallels than distinctions?Immunization with radiation-attenuated Plasmodium berghei sporozoites induces liver cCD8alpha+DC that activate CD8+T cells against liver-stage malaria.The synthetic Plasmodium falciparum circumsporozoite peptide PfCS102 as a malaria vaccine candidate: a randomized controlled phase I trial.Why functional pre-erythrocytic and bloodstage malaria vaccines fail: a meta-analysis of fully protective immunizations and novel immunological model.Extreme CD8 T cell requirements for anti-malarial liver-stage immunity following immunization with radiation attenuated sporozoites.Interleukin-15 enhances innate and adaptive immune responses to blood-stage malaria infection in mice.Invariant Valpha14 chain NKT cells promote Plasmodium berghei circumsporozoite protein-specific gamma interferon- and tumor necrosis factor alpha-producing CD8+ T cells in the liver after poxvirus vaccination of mice.Genetically attenuated, P36p-deficient malarial sporozoites induce protective immunity and apoptosis of infected liver cells.Induction of CD4(+) T cell-dependent CD8(+) type 1 responses in humans by a malaria DNA vaccine.Comparison of Plasmodium berghei challenge models for the evaluation of pre-erythrocytic malaria vaccines and their effect on perceived vaccine efficacy.Differential effector pathways regulate memory CD8 T cell immunity against Plasmodium berghei versus P. yoelii sporozoites.CD4(+) T-cell- and gamma interferon-dependent protection against murine malaria by immunization with linear synthetic peptides from a Plasmodium yoelii 17-kilodalton hepatocyte erythrocyte protein.Early nonspecific immune responses and immunity to blood-stage nonlethal Plasmodium yoelii malaria.Lack of CD4(+) T cells does not affect induction of CD8(+) T-cell immunity against Encephalitozoon cuniculi infection.Expression, extracellular secretion, and immunogenicity of the Plasmodium falciparum sporozoite surface protein 2 in Salmonella vaccine strains.Interleukin-12- and gamma interferon-dependent protection against malaria conferred by CpG oligodeoxynucleotide in mice.Regulation of CD8+ T cell responses to infection with parasitic protozoa.CD8(+)-T-cell immunity against Toxoplasma gondii can be induced but not maintained in mice lacking conventional CD4(+) T cellsPersistence of protective immunity to malaria induced by DNA priming and poxvirus boosting: characterization of effector and memory CD8(+)-T-cell populations.Significant association of KIR2DL3-HLA-C1 combination with cerebral malaria and implications for co-evolution of KIR and HLA.Cross-protection between attenuated Plasmodium berghei and P. yoelii sporozoitesAdministration of recombinant rhesus interleukin-12 during acute simian immunodeficiency virus (SIV) infection leads to decreased viral loads associated with prolonged survival in SIVmac251-infected rhesus macaques.P. falciparum infection durations and infectiousness are shaped by antigenic variation and innate and adaptive host immunity in a mathematical model.Antibody and B cell responses to Plasmodium sporozoites.Immune responses and protection of Aotus monkeys immunized with irradiated Plasmodium vivax sporozoitesCutting edge: attrition of Plasmodium-specific memory CD8 T cells results in decreased protection that is rescued by booster immunization.Plasmodium-host interactions directly influence the threshold of memory CD8 T cells required for protective immunityCD40 is required for protective immunity against liver stage Plasmodium infectionA Plasmodium falciparum candidate vaccine based on a six-antigen polyprotein encoded by recombinant poxviruses.Development of an in vitro assay and demonstration of Plasmodium berghei liver-stage inhibition by TRAP-specific CD8+ T cellsCpG oligodeoxynucleotide and Montanide ISA 51 adjuvant combination enhanced the protective efficacy of a subunit malaria vaccineBone-Marrow-Resident NK Cells Prime Monocytes for Regulatory Function during Infection.Uninfected mosquito bites confer protection against infection with malaria parasitesUnravelling the patterns of host immune responses in Plasmodium vivax malaria and dengue co-infection.Induction of multi-antigen multi-stage immune responses against Plasmodium falciparum in rhesus monkeys, in the absence of antigen interference, with heterologous DNA prime/poxvirus boost immunization.
P2860
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P2860
IL-12 and NK cells are required for antigen-specific adaptive immunity against malaria initiated by CD8+ T cells in the Plasmodium yoelii model.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@ast
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@en
type
label
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@ast
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@en
prefLabel
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@ast
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@en
P1476
IL-12 and NK cells are require ...... n the Plasmodium yoelii model.
@en
P2093
P304
P407
P577
1999-07-01T00:00:00Z