scholarly journals Bovine Holo-Beta-Lactoglobulin Cross-Protects Against Pollen Allergies in an Innate Manner in BALB/c Mice: Potential Model for the Farm Effect

2021 ◽  
Vol 12 ◽  
Author(s):  
Sheriene Moussa Afify ◽  
Isabella Pali-Schöll ◽  
Karin Hufnagl ◽  
Gerlinde Hofstetter ◽  
Maha Abdel-Rafea El-Bassuoni ◽  
...  

The lipocalin beta-lactoglobulin (BLG) is a major protein compound in cow’s milk, and we detected it in cattle stable dust. BLG may be a novel player in the farm protective effect against atopic sensitization and hayfever. In previous studies, we demonstrated that only the ligand-filled holo-form of BLG prevented sensitization to itself. Here, we investigated whether holo-BLG could, in an innate manner, also protect against allergic sensitization to unrelated birch pollen allergens using a murine model. BALB/c mice were nasally pretreated four times in biweekly intervals with holo-BLG containing quercetin–iron complexes as ligands, with empty apo-BLG, or were sham-treated. Subsequently, mice were intraperitoneally sensitized two times with apo-BLG or with the unrelated birch pollen allergen apo-Bet v 1, adjuvanted with aluminum hydroxide. After subsequent systemic challenge with BLG or Bet v 1, body temperature drop was monitored by anaphylaxis imaging. Specific antibodies in serum and cytokines of BLG- and Bet v 1-stimulated splenocytes were analyzed by ELISA. Additionally, human peripheral blood mononuclear cells of pollen allergic subjects were stimulated with apo- versus holo-BLG before assessment by FACS. Prophylactic treatment with the holo-BLG resulted in protection against allergic sensitization and clinical reactivity also to Bet v 1 in an unspecific manner. Pretreatment with holo-BLG resulted in significantly lower BLG-as well as Bet v 1-specific antibodies and impaired antigen-presentation with significantly lower numbers of CD11c+MHCII+ cells expressing CD86. Pretreatment with holo-BLG also reduced the release of Th2-associated cytokines from Splenocytes in BLG-sensitized mice. Similarly, in vitro stimulation of PBMCs from birch pollen allergic subjects with holo-BLG resulted in a relative decrease of CD3+CD4+ and CD4+CRTh2 cells, but not of CD4+CD25+CD127− Treg cells, compared to apo-BLG stimulation. In conclusion, prophylactic treatment with holo-BLG protected against allergy in an antigen-specific and -unspecific manner by decreasing antigen presentation, specific antibody production and abrogating a Th2-response. Holo-BLG therefore promotes immune resilience against pollen allergens in an innate manner and may thereby contribute to the farm protective effect against atopic sensitization.

1996 ◽  
Vol 96 (3) ◽  
pp. 433-438 ◽  
Author(s):  
Ines Swoboda ◽  
Karin Hoffmann-Sommergruber ◽  
Gabriel O'Riordain ◽  
Otto Scheiner ◽  
Erwin Heberle-Bors ◽  
...  

1996 ◽  
Vol 96 (3) ◽  
pp. 433-438 ◽  
Author(s):  
Ines Swoboda ◽  
Karin Hoffmann-Sommergruber ◽  
Gabriel O'Riordain ◽  
Otto Scheiner ◽  
Erwin Heberle-Bors ◽  
...  

1996 ◽  
Vol 98 (5) ◽  
pp. 913-921 ◽  
Author(s):  
Susanne Vrtala ◽  
Peter Mayer ◽  
Fatima Ferreira ◽  
Markus Susani ◽  
Alec H. Sehon ◽  
...  

Vaccine ◽  
2013 ◽  
Vol 31 (46) ◽  
pp. 5405-5412 ◽  
Author(s):  
Martin Schwarzer ◽  
Dagmar Srutkova ◽  
Irma Schabussova ◽  
Tomas Hudcovic ◽  
Johnnie Akgün ◽  
...  

1996 ◽  
Vol 97 (1) ◽  
pp. 95-103 ◽  
Author(s):  
Fatima D. Ferreira ◽  
Peter Mayer ◽  
Wolfgang R. Sperr ◽  
Peter Valent ◽  
Susanne Seiberler ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Oluwatoyin Akinfenwa ◽  
Huey-Jy Huang ◽  
Birgit Linhart ◽  
Margarete Focke-Tejkl ◽  
Susanne Vrtala ◽  
...  

IgE-mediated allergy to birch pollen affects more than 100 million patients world-wide. Bet v 1, a 17 kDa protein is the major allergen in birch pollen responsible for allergic rhinoconjunctivitis and asthma in birch pollen allergic patients. Allergen-specific immunotherapy (AIT) based on therapeutic administration of Bet v 1-containing vaccines is an effective treatment for birch pollen allergy but no allergen-specific forms of prevention are available. We developed a mouse model for IgE sensitization to Bet v 1 based on subcutaneous injection of aluminum-hydroxide adsorbed recombinant Bet v 1 and performed a detailed characterization of the specificities of the IgE, IgG and CD4+ T cell responses in sensitized mice using seven synthetic peptides of 31-42 amino acids length which comprised the Bet v 1 sequence and the epitopes recognized by human CD4+ T cells. We then d.emonstrate that preventive systemic administration of a mix of synthetic non-allergenic Bet v 1 peptides to 3-4 week old mice significantly reduced allergic immune responses, including IgE, IgG, IgE-mediated basophil activation, CD4+ T cell and IL-4 responses to the complete Bet v 1 allergen but not to the unrelated major grass pollen allergen Phl p 5, without inducing Bet v 1-specific allergic sensitization or adaptive immunity. Our results thus demonstrate that early preventive administration of non-allergenic synthetic T cell epitope-containing allergen peptides could be a safe strategy for the prevention of allergen-specific IgE sensitization.


Sign in / Sign up

Export Citation Format

Share Document