TIMING OF LOW-LEVEL NO2 EXPOSURE ALTERS ANTIGEN-SPECIFIC IgE, IgG1, AND IgG2a ANTIBODY PRODUCTION IN MICE

1998 ◽  
Vol 10 (12) ◽  
pp. 1079-1093 ◽  
Author(s):  
Hidekazu Fujimaki
Toxicology ◽  
1997 ◽  
Vol 116 (1-3) ◽  
pp. 227-233 ◽  
Author(s):  
Hidekazu Fujimaki ◽  
Kensaku Saneyoshi ◽  
Fujio Shiraishi ◽  
Toru Imai ◽  
Tomohiko Endo

1994 ◽  
Vol 33 (7) ◽  
pp. 396-401 ◽  
Author(s):  
Tsugio NAKAZAWA ◽  
Shinobu HOUJYO ◽  
Kunio DOBASHI ◽  
Kumiko SATO

2004 ◽  
Vol 95 (2) ◽  
pp. 94-96 ◽  
Author(s):  
Soren Thor Larsen ◽  
Rikke Hansen ◽  
Otto Melchior Poulsen ◽  
Gunnar Damgard Nielsen

2012 ◽  
Vol 129 (2) ◽  
pp. AB235
Author(s):  
R.G. Robison ◽  
M. Makhija ◽  
L.M. Arguelles ◽  
D.M. Caruso ◽  
C. Szychlinski ◽  
...  
Keyword(s):  

2014 ◽  
Vol 59 (1) ◽  
Author(s):  
Niichiro Abe ◽  
Isao Teramoto

AbstractLive Anisakis simplex third-stage larvae (L3) penetrate gastrointestinal mucosa after they are ingested in raw or undercooked seafood, thereafter causing gastrointestinal manifestations and allergic manifestations such as urticaria and anaphylaxis. These allergic reactions are mediated by specific IgE to L3 allergens, especially excretory-secretory (ES) allergens. Recent evidences suggest that only live larvae can cause allergic reactions, although cases attributable to ingestion of cooked, frozen seafood have been reported. Therefore the risk of Anisakis-associated hypersensitivity by ingestion of properly cooked and frozen fish remains controversial. No prior report describes the kinetics of antibody production in experimental animals after oral inoculation with dead L3. This study used ELISA to assess antibody production in rats inoculated orally with dead L3. Positive absorbance value in IgG, IgM, and IgE specific to ES antigen from L3 were found in rats inoculated with live L3 but not with dead L3 (frozen, heated, cut, or homogenized). At one week post re-inoculation with live or frozen L3 to the initially sensitized rats, the absorbance value of the specific IgM and IgE to ES antigen elevated quickly and highly in rats that had been re-inoculated with live L3, but they decreased slightly or did not change in rats inoculated with frozen L3. These results suggest that only ingestion of live L3 can produce the specific antibody and induce initial and secondary sensitizations to L3.


2021 ◽  
Vol 127 (5) ◽  
pp. S114
Author(s):  
C. Cotter ◽  
A. Holsworth ◽  
T. Kelbel
Keyword(s):  

2021 ◽  
Vol 12 ◽  
Author(s):  
Daniel M. Mrochen ◽  
Patricia Trübe ◽  
Ilka Jorde ◽  
Grazyna Domanska ◽  
Cindy van den Brandt ◽  
...  

Protection against Staphylococcus aureus is determined by the polarization of the anti-bacterial immune effector mechanisms. Virulence factors of S. aureus can modulate these and induce differently polarized immune responses in a single individual. We proposed that this may be due to intrinsic properties of the bacterial proteins. To test this idea, we selected two virulence factors, the serine protease-like protein B (SplB) and the glycerophosphoryl diester phosphodiesterase (GlpQ). In humans naturally exposed to S. aureus, SplB induces a type 2-biased adaptive immune response, whereas GlpQ elicits type 1/type 3 immunity. We injected the recombinant bacterial antigens into the peritoneum of S. aureus-naïve C57BL/6N mice and analyzed the immune response. This was skewed by SplB toward a Th2 profile including specific IgE, whereas GlpQ was weakly immunogenic. To elucidate the influence of adjuvants on the proteins’ polarization potential, we studied Montanide ISA 71 VG and Imject™Alum, which promote a Th1 and Th2 response, respectively. Alum strongly increased antibody production to the Th2-polarizing protein SplB, but did not affect the response to GlpQ. Montanide enhanced the antibody production to both S. aureus virulence factors. Montanide also augmented the inflammation in general, whereas Alum had little effect on the cellular immune response. The adjuvants did not override the polarization potential of the S. aureus proteins on the adaptive immune response.


1996 ◽  
Vol 26 (12) ◽  
pp. 1420-1427 ◽  
Author(s):  
T. BRUNNEE ◽  
A. SEEBERGER ◽  
J. KLEINE-TEBBE ◽  
G. KUNKEL

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