scholarly journals Allergen-Specific Immunotherapy With Liposome Containing CpG-ODN in Murine Model of Asthma Relies on MyD88 Signaling in Dendritic Cells

2020 ◽  
Vol 11 ◽  
Author(s):  
Ricardo Wesley Alberca-Custodio ◽  
Lucas D. Faustino ◽  
Eliane Gomes ◽  
Fernanda Peixoto Barbosa Nunes ◽  
Mirian Krystel de Siqueira ◽  
...  
2005 ◽  
Vol 19 (9) ◽  
pp. 1152-1154 ◽  
Author(s):  
Mila Ayash‐Rashkovsky ◽  
Gadi Borkow ◽  
Heather L. Davis ◽  
Ronnald B. Moss ◽  
Richard Bartholomew ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Guillem Montamat ◽  
Cathy Leonard ◽  
Aurélie Poli ◽  
Ludger Klimek ◽  
Markus Ollert

Prevalence and incidence of IgE-mediated allergic diseases have increased over the past years in developed and developing countries. Allergen-specific immunotherapy (AIT) is currently the only curative treatment available for allergic diseases that has long-term efficacy. Although AIT has been proven successful as an immunomodulatory therapy since its beginnings, it still faces several unmet needs and challenges today. For instance, some patients can experience severe side effects, others are non-responders, and prolonged treatment schedules can lead to lack of patient adherence and therapy discontinuation. A common strategy to improve AIT relies on the use of adjuvants and immune modulators to boost its effects and improve its safety. Among the adjuvants tested for their clinical efficacy, CpG oligodeoxynucleotide (CpG-ODN) was investigated with limited success and without reaching phase III trials for clinical allergy treatment. However, recently discovered immune tolerance-promoting properties of CpG-ODN place this adjuvant again in a prominent position as an immune modulator for the treatment of allergic diseases. Indeed, it has been shown that the CpG-ODN dose and concentration are crucial in promoting immune regulation through the recruitment of pDCs. While low doses induce an inflammatory response, high doses of CpG-ODN trigger a tolerogenic response that can reverse a pre-established allergic milieu. Consistently, CpG-ODN has also been found to stimulate IL-10 producing B cells, so-called B regulatory cells (Bregs). Accordingly, CpG-ODN has shown its capacity to prevent and revert allergic reactions in several animal models showing its potential as both preventive and active treatment for IgE-mediated allergy. In this review, we describe how CpG-ODN-based therapies for allergic diseases, despite having shown limited success in the past, can still be exploited further as an adjuvant or immune modulator in the context of AIT and deserves additional attention. Here, we discuss the past and current knowledge, which highlights CpG-ODN as a potential adjuvant to be reevaluated for the enhancement of AIT when used in appropriate conditions and formulations.


2017 ◽  
Vol 174 (2) ◽  
pp. 86-96 ◽  
Author(s):  
Nicki Yat Hin Leung ◽  
Christine Yee Yan Wai ◽  
Shang An Shu ◽  
Christopher C. Chang ◽  
Ka Hou Chu ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Maria J. Rodriguez ◽  
Andrea Wangorsch ◽  
Francisca Gomez ◽  
Stefan Schülke ◽  
Maria J. Torres ◽  
...  

Background. The use of hypoallergenic derivatives is considered beneficial to promote the safety and efficacy of allergen-specific immunotherapy. We aimed to assess the efficacy of reduced and alkylated (R/A) Pru p 3, a hypoallergenic folding variant of the major peach allergen, in subcutaneous immunotherapy (SCIT) using a murine model of peach allergy. Methods and Results. After sensitization with Pru p 3, BALB/c mice received SCIT with Pru p 3 or R/A Pru p 3 and were challenged with Pru p 3. SCIT with Pru p 3, but not with R/A Pru p 3, suppressed anaphylaxis upon the challenge significantly. SCIT with Pru p 3 did not suppress Pru p 3-specific IgE and IgG1 production, but enhanced IgG2a production. In contrast, SCIT with R/A Pru p 3 suppressed IgE and IgG1 production, but enhanced IgG2a production only moderately. The therapeutic efficacy of SCIT with Pru p 3 was associated with induction of IL-10 and IFN-γ. Conclusion. Hypoallergenic folding variant of Pru p 3 is not likely an efficacious therapeutic component in SCIT of peach allergy. The lower efficacy of R/A Pru p 3 might be attributed to poor antigenicity and/or weak stability due to its unfolded conformation.


PLoS ONE ◽  
2017 ◽  
Vol 12 (6) ◽  
pp. e0178563 ◽  
Author(s):  
Antonio Aguilar-Pimentel ◽  
Anke Graessel ◽  
Francesca Alessandrini ◽  
Helmut Fuchs ◽  
Valerie Gailus-Durner ◽  
...  

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