Table 2.
Allergen | Sensitization | Challenge | Readout | Ref. |
Chaw components (wheat, soy bean, wheat middlings, yellow corn,fish meal) | Was−/−, Was−/− Il4−/−, Was−/− Rag2−/− mice: none (spontaneous sensitization) | None (spontaneous sensitization)orstarving for 3 h then fed 12.5 mg soy protein in 300 μl PBS | Surface LAMP-1,Intestinalmast cell expansion,Serum levels of mast cell protease 1 (MCPT1),body temperature by transponder | [46] |
Cyp c 1;Hypoallergenic mCyp c 1;carp extract | C3H/HeJ mice: 5× i.g. weekly 100 mg rCyp c 1 + 20 mg cholera toxin in 200 ml 0.2-mol bicarbonate buffer (pH 9)20 mg hypoallergenic mCyp c 1 + Alum s.c. 6 times every month;Carp extract–sensitized C3H/HeJ, 600 ml of heat-inactivated mCyp c 1-specific mouse antisera i.p. | i.g. 100 mg rCyp c 1i.g. 10 mg carp extract | Symptom score | [56] |
OVA | BALB/c mice: 2× i.p. 50 mg of OVA + Alum + magnesium hydroxide | 5× i.g. 50 mg of OVA every other day | Diarrhea,rectal temperature | [55] |
OVA | BALB/c mice: gavaged daily with diosgenin | repeatedly i.g.OVA | Foxp3+ Treg cells coexpressing Th1-type transcription factors, cytokines, chemokines in intestine,mRNA expression of chemokines corresponding to Th1-like Treg cells | [58] |
OVA | C57BL/6 mice or TLR5−/−:i.g. 0.1 mg OVA/mouse ± flagellin + cholera toxin (0.02 mg/mouse) weekly for 4 consecutive weeks | gavage-fed OVA (10 mg/mouse in 0.3 ml physiological saline) | Mast cell infiltration in the intestinal mucosa, intestinal CD4+ T-cell proliferation, core temperature, diarrhea | [48] |
OVA | BALBc/c mice: 2× i.p. 20 μg OVA + Alum | 5× orally 50 mg OVA every 3 days;Baicalein (20 mg/kg) orally administered daily from day 28–40 | Diarrhea, anaphylaxis,rectal temperature | [59] |
OVA | C57BL/6 mice or miR-17–92fl/fl: fed OVA 1 mg/mouse + cholera toxin (20 μg/mouse) weekly for 4 weeks;wild and miR-19a-deficient mice with recombinant IL-4 or/and LPS via i.p. injection daily for 5 days | Mast cell and eosinophil infiltration in intestinal mucosa, allergen-specific CD4+ T cells in the intestine;B cells isolated from intestine analyzed for IL-10 expression | [49] | |
OVA | BALB/C (AnNR/J) mice: i.p. 2 × 10 mg OVA + Alum | OVA p.o. (20 mg/mouse), 5× within a 10-day period | Rectal body temperature,clinical score (diarrhea severity, appearance of hirsute pelage) | [54] |
OVA | OVA (2 mg) i.g. 3×/week for lactating mothers 3 weeks after delivery or during lactation period ± VitA supplemention by maternal vitamin A-enriched diet from 2 days before delivery until the end of first week | 6–8-week-old adult mice: allergic airway inflammation to OVA by i.p. 10 mg OVA + Alum on days 0 and 7, day 17–21 mice exposed to OVA (0.5%) aerosols for 20 min in nebulizer | Serum OVA-specific IgE, IgA,eosinophils BAL;lung cell cytokinesecretion;ex vivo gut permeability;small intestine histology;serum retinol levels | [50] |
Peanut extract | NOD-scid IL2Rgammanull mice: transferred i.p. 3 × 107 bloodmononuclear cells from peanut allergic donors + 100 mg crude peanut extract;i.p. 2× 100 mg of crude peanut extract;therapy: AAVrh.10 anti-hIgE (1011 genome copies)at week 3, reconstituted with human donor blood mononuclear cells at week 0 | i.g. 300 mg crude peanut extract at weeks 5–10 | Clinical score,anaphylaxis score,histamine in plasma,PCA | [53] |
Peanut butter | huNSG mice: i.g. 22.5 mg (5 mg protein) skippy creamy peanut butter in 250 ml 0.2 mol sodium bicarbonate, pH 8.0, weekly for 8 weeks | Fed 350 mg peanut butter in 0.2 mol sodium bicarbonate | Temperature measurements using s.c. microchip transponders;PN-specific human IgE in serum;tissue mast cell expansion | [44▪▪] |
Peanut extract,pAra h 2,PLL-pAra h 2 | BALB/c mice: i.d.PLL-pAra h 2 or pAra h 2 (25 μg pAra h 2 DNA) 3×, followed i.p. 2.5 μg purified Ara h 2 + Alum | i.p. 5 mg CPE | Rectal temperature | [57] |
Peanut extract | i.p. 3× 500 mg peanut extract + Alum at 1 week interval | 7× orally peanut extract (15 mg) every 2 days | Body temperature, clinical symptoms:activity/lethargy, diarrhea, death | |
Peanut | C3H/HeJ mice: oralpeanut + cholera toxin;therapy: 4× fed CpG/PN-nanoparticles | 5× monthly oral peanut | Visualsymptom scores, body temperature | [51] |
Different allergens according to allergy of human donors | NOD.CB17-Prkdcscid/J γc−/−mice i.p. with 1 × 107 PBMCs from donors allergic to different allergens ± Treg cells (ratio of 1 : 10 or 1 : 20) ± respective allergen (20 mg) ± 4 mghuman recombinant GARP | i.p. allergen boost200 ml 0.9% NaCl | High-resolutionvideo endoscopicrectally | [45] |
Peanut paste | Atopic beagles:e.c. 2× weekly for 8 weeks under occlusion on the axillae | Day 56: orally with roasted peanut (2 g/kg)day 66 e.c. peanut paste on one pinna under occlusion | Systemic signs (e.g. vomiting, diarrhea, collapse), pruritus, CADESI,skin biopsies | [10] |
AAVrh.10anti-hIgE, adeno-associated rh.10 serotype vector coding for a full-length, high-affinity, antihIgE antibody from Fab fragment of anti-hIgE mAb omalizumab; Alum, aluminum hydroxide; e.c., epicutaneous; GARP. glycoprotein A repetitions predominant; huNSG, nonobese diabetic severe combined immunodeficient common gamma chain-deficient stem cell factor; i.d., intradermal; i.g., intragastric; i.p., intraperitoneal; LPS, lipopolysaccharide; OVA, ovalbumin; p.o., per os; pAra h 2, plasmid encoding Ara h 2; PBMC, peripheral blood mononuclear cells; PCA, passive cutaneous anaphylaxis; PN, peanut; PLL-pAra h 2, pAra h 2 pretreated with poly-L-lysine; WASP, Wiskott–Aldrich syndrome protein.