2002
DOI: 10.1006/cyto.2002.1980
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SERUM ANTIBODY RESPONSE AND NASAL LYMPHOID TISSUE (NALT) STRUCTURE IN THE ABSENCE OF IL-4 OR IFN-γ

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Cited by 4 publications
(6 citation statements)
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“…Sera antibody responses accompanying these immunization regimes were predominantly IgG (81, 82). Similar findings were obtained in gene knockout mice (92). IgA was not detectable in sera or gut washes but was found readily in nasal washes (81, 82).…”
Section: Immune Responsessupporting
confidence: 86%
See 1 more Smart Citation
“…Sera antibody responses accompanying these immunization regimes were predominantly IgG (81, 82). Similar findings were obtained in gene knockout mice (92). IgA was not detectable in sera or gut washes but was found readily in nasal washes (81, 82).…”
Section: Immune Responsessupporting
confidence: 86%
“…In other experiments, IN antigen exposure elicited IgA responses in salivary, respiratory, intestinal, and vaginal secretions (86, 94). IN infection with influenza virus (92) or respiratory syncytial virus (93) elicited antigen‐specific IgA‐secreting cells in the NALT and cervical lymph nodes, again suggesting NALT cell traffic. These findings are consistent with NALT cell trafficking capability, especially to distant mucosae and to peripheral lymph nodes (82, 91), but this finding has yet to be confirmed by specific cell trafficking studies.…”
Section: Immune Responsesmentioning
confidence: 99%
“…Construction, amplification, purification of nonreplicative recombinant adenovirus expressing the human TSHR A subunit (Ad‐TSHR289) and determination of the viral particle concentration were performed as previously described [7]. Female wild type (wt) BALB/c mice (eight to 12 weeks old; Charles River Laboratory Inc., Tokyo, Japan) and IFN‐ γ KO and IL‐4 KO BALB/c mice (Jackson Laboratory Inc., Bar Harbor, ME, USA) [8] were injected in the quadriceps with 100 µ l PBS containing 10 10 particles of Ad‐TSHR289 twice at a three‐week‐interval. Blood, spleens and thyroid tissues were obtained two weeks after the second immunization.…”
Section: Methodsmentioning
confidence: 99%
“…Nesse ponto, as vacinas administradas pelas vias intranasal ou oral induzem a produção de IgA local via NALT e o desenvolvimento de imunidade mediada por células específicas nos tratos respiratório e gastrointestinal, respectivamente. A IgA local protege contra a invasão de agentes infecciosos e é um benefício significativo em doenças que envolvem principalmente estas áreas (DHEIN;GORHAM, 1986;STRAVER, 1989;HALL et al, 1991;HERITAGE et al, 1997HERITAGE et al, , 1998ANDOH et al, 2002;HISHIKI et al, 2004).…”
Section: Vias De Administraçãounclassified
“…Muitos estudos identificaram que existe grande contribuição local de IgA à defesa imune do trato respiratório contra uma variedade de agentes potencialmente patogênicos associada a papel específico de tecidos linfoides associados à mucosa, como o NALT (DHEIN;GORHAM, 1986;HERITAGE et al, 1997HERITAGE et al, , 1998ANDOH et al, 2002;HISHIKI et al, 2004).…”
Section: Pesquisa De Anticorposunclassified