scholarly journals Oral immunization of a rAd vector expressing norovirus VP1 elicits a potent mucosal immune response without an increase in anti-vector immunity

2018 ◽  
Vol 73 ◽  
pp. 69
Author(s):  
S. Tucker ◽  
L. Kim ◽  
D. Liebowitz ◽  
K. Lin ◽  
K. Kasparek ◽  
...  
1999 ◽  
Vol 67 (2) ◽  
pp. 520-526 ◽  
Author(s):  
Wim Van den Broeck ◽  
Eric Cox ◽  
Bruno M. Goddeeris

ABSTRACT F4 receptor-positive (F4R+) and F4 receptor-negative (F4R−) pigs were orally vaccinated with purified F4 fimbriae of enterotoxigenic Escherichia coli (ETEC). Serum immunoglobulin G (IgG) and IgA responses were readily detected in F4R+ animals, whereas immune responses were not detected in F4R− animals. Even after a subsequent oral infection with virulent F4+ ETEC and a booster immunization with F4, the F4R− animals remained F4 seronegative whereas the unvaccinated F4R+ pigs exhibited clear IgA and IgG responses. These results clearly demonstrate that F4Rs are a prerequisite for an immune response following oral immunization. Furthermore, indications that oral F4 vaccination can induce mucosal protection were obtained, since the experimental ETEC infection did not induce a systemic booster response or fecal ETEC excretion in orally vaccinated F4R+ pigs, in contrast to the clear immune response and ETEC excretion of unvaccinated F4R+ animals. F4-specific IgA antibodies could be found in the feces of the vaccinated F4R+ pigs. They are secreted at the intestinal mucosal surface and appear to prevent ETEC infection. The F4R-dependent induction of a mucosal immune response can be used as a model to better understand mucosal immunization and mucosal immune responses and can contribute to the development of oral vaccines in veterinary as well as in human medicine.


1983 ◽  
Vol 157 (2) ◽  
pp. 572-582 ◽  
Author(s):  
S N Emancipator ◽  
G R Gallo ◽  
M E Lamm

To test the hypothesis that IgA nephropathy can result from a mucosal immune response, mice were orally immunized with one of three protein antigens for 14 wk. Such mice exhibited an essentially pure mucosal antibody response characterized by specific IgA-producing plasma cells in exocrine sites and specific IgA antibodies in serum. Furthermore, 73% of immunized mice had IgA and 88% had immunogen deposited in the glomerular mesangium, and 64% of immunized mice examined ultrastructurally had electron-dense mesangial deposits. All three were present concurrently in 57% of the immunized mice. No differences in regard to IgG or IgM were observed between immunized and control mice for any of these parameters. Mucosal immunization therefore can result in a specific immune response that leads to mesangial deposition of immune complexes containing IgA antibody. In its fundamental features the experimental renal lesion resembles that seen in the human disease IgA nephropathy.


2021 ◽  
Vol 113 ◽  
pp. 185-195
Author(s):  
Tasok Leya ◽  
Irshad Ahmad ◽  
Rajendran Kooloth Valappil ◽  
Pani Prasad Kurcheti ◽  
Gayatri Tripathi ◽  
...  

1999 ◽  
Vol 43 (3) ◽  
pp. 253-258 ◽  
Author(s):  
Takeyuki Kohno ◽  
Hiroko Tanaka ◽  
Kazuhito Watabe ◽  
Shinji Yamashita ◽  
Hitoshi Sezaki ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (10) ◽  
pp. e47979 ◽  
Author(s):  
John Wei ◽  
Shiven Bhatt ◽  
Lisa M. Chang ◽  
Hugh A. Sampson ◽  
Madhan Masilamani

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