Table 1.
Approach | Study subjects and inclusion criteria | Immunizing reagent | Effects | Publication |
---|---|---|---|---|
Subcutaneous immunotherapy | Human adults including those with anaphylaxis | Peanut extract | ↑ oral tolerance and ↓ SPT; high rate of systemic reactions |
1997 [15] |
OIT | Children with no history of severe anaphylaxis | Peanut flour | 54–84% desensitized to target maintenance doses; side effects in 47 and 81% of treated subjects; ↑ IgG4 |
2011 [16] and 2014 [18] |
SLIT | Children [31] and adults [32] with no history of severe anaphylaxis | Liquid peanut extract | ↑ oral tolerance; mild side effects; ↓ SPT; ↑ IgG4 and ↓ basophil activation |
2011 [31] and 2013 [32] |
EPIT | Children with no history of severe anaphylaxis | Patch containing 100 μg of peanut proteins | ↑ oral tolerance in up to 67% mild side effects; ↑ IgG4 |
2014 [41] |
Recombinant hypoallergenic peanut allergens and bacterial adjuvants | Human adults with no history of severe anaphylaxis | mAra h 1–3 plus heat/phenol-inactivated E. coli | ↓ SPT; ↓ basophil activation; high rate of systemic reactions |
2013 [52] |
Recombinant hypoallergenic peanut allergens | Murine model of peanut anaphylaxis | mAra h 2 | Reduced clinical symptom scores and histamine release | 2001 [48] |
RBL-2H3 cells and PBMCs from 4 peanut-allergic patients | mAra h 2 | Partially reduced IgE reactivity with retained T cell reactivity | 2005 [45] | |
Peanut extract and bacterial adjuvants | Brown Norway rat model for peanut allergy | Peanut extract plus L. casei Shirota | Downregulation of peanut allergic response in 2 of 8 rats | 2008 [69] |
Balb/c mice | Peanut extract, cholera toxin and CpG | Prevention of oral sensitization by previous subcutaneous administration of the mix | 2007 [131] | |
Peanut-allergic C3H/HeJ mice | Modified Ara h 1–3 plus HKLM | Reduced histamine levels, peanut-specific IgE, bronchial constriction and anaphylaxis symptoms | 2003 [50] | |
Peanut-allergic C3H/HeJ mice | HKE-mAra h 1–3 | Reduced production of IL-4, IL-5 and IL-13 by splenocytes and long-term downregulation of peanut hypersensitivity | 2003 [51] | |
T cell epitope-based peptide vaccines | Peanut-allergic C3H/HeJ mice | 30 overlapping Ara h 2 20-mers | Reduced histamine release and anaphylaxis symptoms | 2007 [81] |
DNA-based vaccines | AKR/J mice | Complex of chitosan and Ara h 2-encoding DNA | Reduction of peanut-induced anaphylaxis, reduced level of IgE | 1999 [86] |
AKR/J, Balb/c and C3H/HeJ mice | Plasmid DNA encoding Ara h 2 | Strain-dependent induction of allergic sensitization | 1999 [87] | |
Hypoallergenic transgenic plants | Western blot with sera from peanut-allergic patients | Seed proteins from transgenic peanut plants with silenced Ara h 2 and Ara h 6 | Significant reduction of IgE-binding | 2008 [96] |