scholarly journals IgE antibodies increase honeybee venom responsiveness and detoxification efficiency of mast cells

Allergy ◽  
2021 ◽  
Author(s):  
Philipp Starkl ◽  
Nicolas Gaudenzio ◽  
Thomas Marichal ◽  
Laurent L. Reber ◽  
Riccardo Sibilano ◽  
...  
2017 ◽  
Vol 263 ◽  
pp. e9
Author(s):  
Alexia Loste ◽  
Marc Clément ◽  
Sandrine Delbosc ◽  
Anh Thu Gaston ◽  
Marion Morvan ◽  
...  
Keyword(s):  

1985 ◽  
Vol 27 (4) ◽  
pp. 179-185 ◽  
Author(s):  
T. A. Mota-Santos ◽  
A. F. S. Oliveira ◽  
S. E. Gerken ◽  
N. M. Vaz

Methods generally utilized for studies on anaphylaxis to protein antigens such as determination of histamine release to the blood, hemoconcentration, histamine release from peritoneal mast cells and passive cutaneous anaphylaxis (PCA) were used to investigate some aspects of the anaphylaxis to parasite antigens in Schistosoma mansoni infected mice. The release of histamine to the blood and significant rates of hemoconcentration were induced by intravenous injection of schistosomula or cercarial extracts into 10-13 weeks infected mice. Cercarial, schistosomula, worm tegument and soluble egg antigens were able to trigger histamine release from peritoneal mast cells from chronically infected mice. In spite of the PCA reaction beeing detected within 2 hours of sensitization (IgG1antibodies) in 6 of 8 tested sera from chronically infected mice, no detectable reactions were obtained after 48 hours sensitization (IgE antibodies). Although IgE was not detected in the circulation, by the PCA technique, the results indicate that the infected mice contained IgE antibodies bound to their mast cells.


2018 ◽  
Vol 20 (1) ◽  
pp. 45 ◽  
Author(s):  
Yuhki Yanase ◽  
Yoshimi Matsuo ◽  
Tomoko Kawaguchi ◽  
Kaori Ishii ◽  
Akio Tanaka ◽  
...  

Basophils and mast cells have high affinity IgE receptors (FcεRI) on their plasma membrane and play important roles in FcεRI-associated allergic diseases, such as pollen allergy, food allergy, chronic spontaneous urticarial (CSU), and atopic dermatitis (AD). To date, several reports have revealed that high IgE antibody concentrations activate mast cells—which reside in tissue—in the absence of any antigens (allergens). However, IgE antibody-induced activation of basophils—which circulate in blood—has not been reported. Here, we investigated whether IgE antibodies may regulate functions of human peripheral basophils without antigens in vitro. We successfully removed IgE antibodies bound to FcεRI on the surface of human peripheral basophils by treating with 0.1% lactic acid. We also demonstrated that high IgE antibody concentrations (>1 μM) induced histamine release, polarization, and CD203c upregulation of IgE antibody-stripped basophils. Thus, high IgE antibody concentrations directly activate basophils, which express IgE-free FcεRI on the cell surface. This mechanism may contribute to the pathogenesis of patients with AD and CSU who have higher serum IgE concentrations compared to healthy donors.


2009 ◽  
Vol 132 (1) ◽  
pp. 53-61 ◽  
Author(s):  
Bettina Wagner ◽  
William H. Miller ◽  
Hollis N. Erb ◽  
D. Paul Lunn ◽  
Douglas F. Antczak
Keyword(s):  

2019 ◽  
Vol 31 (4) ◽  
pp. 969-974
Author(s):  
Mire Spasov ◽  
Icko Gjorgoski

The allergic reaction or type I hypersensitivity is a hypersensitive disorder to the immune system, which occurs by ingress of non-pathogenic agents from the external environment in the body. Antigens, in this case allergens, are substances from the environment that are harmless to most people. In allergies there is an inherent tendency to inherit the genes that make these people susceptible to allergies. Rapid sensitization may occur as a local reaction, which is just unpleasant (seasonal rhinitis or hay fever), severe exhaustion (asthma), or culminating in a fatal systemic disorder (anaphylaxis). Allergens in the body are inserted by inhalation, ingestion or injection, and move to mucous membranes, where they are accepted by T-lymphocytes. TN2 lymphocytes produce IL-4, which stimulate B-lymphocytes to differentiate into plasma cells. These cells excrete IgE, which recognize allergens. Excreted IgE antibodies sensitize mast cells that originate from the bone marrow. When sensitized individuals again expose themselves to an allergen from the external environment, they bind to specific IgE-antibodies to the mast cells (memory cells), whereby various mediators are excreted, causing inflammatory response, mucus secretion, vasoconstriction of blood vessels, and spasm of the airways. The aim of the study was to investigate the allergenic effect of Daucus carotte on the change in the number of leukocytes, lymphocytes, monocytes, granulocytes, basophils, and immunoglobulins as important components of the immune system. From the pollen of this plant, recombinant allergen is extracted, in the form of injections with a volume of 150μI. In the experiments, as experimental models were used Wistar white rats at the age of 6 to 9 weeks. We injected the allergen into the first, second, third and fourth week in a group of 6 rats in an amount of 5 μl and a second group of 6 rats in an amount of 2.5 μl allergen absorbed in 100 μl AI (OH) 3 (Serva, Heidelburg, Germany, 2 μg / mI) in a total volume of 150μI sterile PbS. The third group of 6 rats was a control group. The results showed that the Dacus carota causes an allergic reaction in Wistar white rats and its intensity depends directly on the volume of the allergen and the individuals that come into contact with it. Once we compared the values of blood parameters, leukocytes, lymphocytes, monocytes, granulocytes, and basophils, as well as the IgG, IgG1, IgG2a, and IgE IgG, IgG1, IgG2a, and IgE concentrations, we concluded that the higher concentration of Daucus carota causes a higher elevation in blood parameters and concentrations of immunoglobulins, compared to the smaller concentration of the same allergen. From the studies conducted over a period of one month, it was found that Dacus carota causes an allergic reaction, which is classified in Type I hypersensitivity in white laboratory rats of the Wistar strain.


1985 ◽  
Vol 77 (1-2) ◽  
pp. 238-240 ◽  
Author(s):  
S. Ahlstedt ◽  
B. Björkstén ◽  
J. Borwell ◽  
I. Hammarström ◽  
J.-O. Nybacka

2014 ◽  
Vol 133 (2) ◽  
pp. AB225
Author(s):  
Philipp Starkl ◽  
Thomas Marichal ◽  
Laurent L. Reber ◽  
Janet Kalesnikoff ◽  
Hans C. Oettgen ◽  
...  

Blood ◽  
1989 ◽  
Vol 74 (3) ◽  
pp. 925-929
Author(s):  
A Kuriu ◽  
S Sonoda ◽  
Y Kanakura ◽  
K Jozaki ◽  
A Yamatodani ◽  
...  

The fate of mast cells after degranulation was investigated. Purified peritoneal mast cells of WBB6F1-+/+ mice were sensitized with monoclonal anti-dinitrophenol (DNP) IgE antibodies and stimulated with DNP conjugated with human serum albumin. Mast cells were vitally stained with neutral red, and highly degranulated mast cells were identified under a phase-contrast microscope and individually picked up with the micromanipulator. When these highly degranulated mast cells were individually plated in methylcellulose, their potential to produce a cluster or a colony was comparable to that of morphologically intact mast cells. Moreover, when highly degranulated mast cells were injected into the skin of genetically mast cell-deficient WBB6F1-W/Wv mice, the proportion of injection sites at which mast cell clusters appeared was comparable to the value observed when morphologically intact mast cells were injected. The present result indicates that proliferative potential of mast cells is not reduced by their degranulation.


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