2007
DOI: 10.4049/jimmunol.178.4.2370
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Mucosal HIV-1 Pox Virus Prime-Boost Immunization Induces High-Avidity CD8+ T Cells with Regime-Dependent Cytokine/Granzyme B Profiles

Abstract: The quality of virus-specific CD8+ CTL immune responses generated by mucosal and systemic poxvirus prime-boost vaccines were evaluated in terms of T cell avidity and single-cell analysis of effector gene expression. Intranasal (I.N.) immunization regimes generated higher avidity CTL responses specific for HIV KdGag197–205 (amino acid sequence AMQMLKETI; H-2Kd binding) compared with i.m. immunization regime. Single-cell RT-PCR of KdGag197–205-specific mucosal and systemic CTL revealed that the cytokine and gran… Show more

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Cited by 77 publications
(81 citation statements)
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“…Similar findings have been reported when mucosal and systemic poxvirus prime-boost routes of immunization were evaluated [102]. Mucosal (intranasal) immunization regimens induced higher avidity CD8 + T cells compared with intramuscular vaccination.…”
Section: Reviewsupporting
confidence: 77%
See 1 more Smart Citation
“…Similar findings have been reported when mucosal and systemic poxvirus prime-boost routes of immunization were evaluated [102]. Mucosal (intranasal) immunization regimens induced higher avidity CD8 + T cells compared with intramuscular vaccination.…”
Section: Reviewsupporting
confidence: 77%
“…Mucosal (intranasal) immunization regimens induced higher avidity CD8 + T cells compared with intramuscular vaccination. CD8 + CTLs expressing high levels of granzyme B were observed in the genital tract after mucosal HIV-1 recombinant homologous primeboost immunization [102]. Intranasal (mucosal) primewith intramuscular (systemic) boost immunization elicited a higher number of granzyme B-positive CD8 + CTLs in genital mucosa compared with an intramuscular primeboost protocol.…”
Section: Reviewmentioning
confidence: 95%
“…The route of immunization and vaccine delivery regimen are important variables in the in generation of functionally active and effective HIV-1-specific CD8 + CTL and antibody responses in mucosal and systemic sites [5,6,8,13,14,29,38,39,42,65,[109][110][111][112][113]. Our recent study demonstrates that mucosal prime and boost immunizations are essential to the induction of high avidity CD8 + CTL responses in inductive and effector sites of gastrointestinal mucosa, while IR vaccination with rMVA alone was not effective in generation of high avidity CD8 + CTL in the gut mucosa [38].…”
Section: Generation Of Functional Active Hiv-1-specific Immune Responmentioning
confidence: 99%
“…We chose to design a nested PCR reaction for each molecule to provide a highly sensitive means to detect these molecules in low cell sample numbers as used in murine experiments. 5,6 The multiplex primers were designed to result in bands with differing sizes readily detected on the final gel. With this assay we were able to readily detect all four cytolytic molecules from M. nemestrina bulk PBMCs together with CD8 and LAMP-1 (Fig.…”
Section: Rollman Et Al 1128mentioning
confidence: 99%
“…Granzymes and perforin molecules are differentially expressed in single CD8 T cells in murine influenza infection models, highlighting the complexity of mammalian cytotoxic molecules. 5,6 Several simian models of HIV-1 infection exist, with the most commonly studied models being SIV infection of rhesus (Macaca mulatta), and, increasingly, cynomolgus (M. fascicularis) and pigtail macaques (M. nemestrina). Most studies of cytotoxic molecules in nonhuman primates have employed only rhesus macaques.…”
mentioning
confidence: 99%