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. Author manuscript; available in PMC: 2020 Sep 1.
Published in final edited form as: J Allergy Clin Immunol Pract. 2019 Mar 30;7(7):2348–2358.e4. doi: 10.1016/j.jaip.2019.03.031

TABLE II.

(A) Component analysis of subjects reporting allergic reactions to red meat but not having α-Gal sIgE ≥ 0.35 IU/mL. (B) Component analysis of 2 subjects reporting allergic reactions to red meat with α-Gal sIgE ≥ 0.35 IU/mL, but component signature suggestive of pork-cat syndrome

Demographic Timing Total IgE α-Gal Beef Pork Milk Cat Fel d 2 Sus s 1
(A) Component analysis of subjects reporting allergic reactions to red meat but not having α-Gal sIgE ≥ 0.35 IU/mL
 Low titer α-Gal
  42 M 6 h 113 0.26 0.22 0.13 0.19 <0.10 0.13 nd
  49 F 4-8 h 25 0.18 <0.10 <0.10 <0.10 <0.10 <0.10 nd
  58 F 0:20-0:30 62 0.16 nd nd Nd nd nd nd
  52 F 0:30 13 0.16 <0.10 <0.35 <0.10 <0.10 <0.10 nd
  30 M 1:30 356 0.19 <0.10 <0.10 <0.10 <0.10 <0.10 nd
 Suggestive of primary beef allergy
  68 F 2 h 85 0.2 0.42 0.11 0.24 <0.10 <0.10 nd
  47 F 4 h 5 <0.10 1.30 <0.10 <0.35 <0.35 <0.35 nd
  42 F 3 h 1157 <0.10 0.18 0.11 <0.35 <0.35 <0.10 nd
 Suggestive of pork-cat syndrome
  51 M 1 h 83 <0.10 <0.10 0.65 <0.35 3.74 2.28 0.62
  16 M 6-8 h 277 <0.10 <0.10 0.28 0.11 2.83 0.10 0.19
  43 F 0:15-5 h 42 <0.35 <0.35 0.37 <0.35 3.87 4.18 nd
 No component diagnosis
  32 F 2 h 71 <0.10 <0.10 <0.10 <0.10 <0.35 <0.35 nd
  50 F 6 h 88 <0.10 <0.10 <0.10 <0.10 <0.10 <0.10 nd
  45 F 0:30-1 h 22 <0.10 <0.10 <0.10 <0.10 <0.10 <0.10 nd
  20 M 4 h 74 <0.10 <0.10 <0.10 <0.10 0.13 <0.10 nd
  28 M 6 h 63 <0.10 <0.10 <0.10 <0.10 <0.10 <0.10 nd
(B) Component analysis of 2 subjects reporting allergic reactions to red meat with α-Gal sIgE ≥ 0.35 IU/mL but component signature suggestive of pork-cat syndrome
  47 F 8-12h 197 0.62 0.11 3.40 <0.10 17.70 26.80 0.28
  21 F 0:05 328 1.41 1.10 7.10 5.08 5.71 12.30 nd

α-Gal, Galactose-α-1,3-galactose; sIgE, specific IgE.

Key for demographics and symptom onset: shown are age (y), sex (M-male, F-female), and time (min) between mammalian meat ingestion and self-reported symptom onset (in cases with 2 values a range of times were reported, reflecting onset during different allergic reactions). All values expressed in IU/mL. Limit of detection varied as either 0.10 IU/mL or 0.35 IU/mL, as indicated; nd denotes serum was not available for assay; values in bold type indicate labs that are consistent with the relevant syndrome.