CoChat
Sign Up
Cited by 77

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Galactose α-1,3-galactose phenotypes

Levin, Michael, Apostolovic, Danijela, Biedermann, Tilo, Commins, Scott P., Iweala, Onyinye I., Platts-Mills, Thomas A.E., Savi, Eleonora, van Hage, Marianne, Wilson, Jeffrey M.·2019·Annals of Allergy, Asthma & Immunology
DOI 10.1016/j.anai.2019.03.021PMC PMC6839685
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.anai.2019.03.021

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 1 references

Research works printed but not linked: 58

  1. Koike, 2007, Functionally important glycosyltransferase gain and loss during catarrhine primate emergence, Proc Natl Acad Sci U S A, 104, 559, 10.1073/pnas.0610012104 · DOI
  2. Galili, 2013, Anti-gal: an abundant human natural antibody of multiple pathogeneses and clinical benefits, Immunology, 140, 1, 10.1111/imm.12110 · DOI · Paper page
  3. Galili, 2015, Significance of the evolutionary α1,3-galactosyltransferase (GGTA1) gene inactivation in preventing extinction of apes and old world monkeys, J Mol Evol, 80, 1, 10.1007/s00239-014-9652-x · DOI
  4. Van Nunen, 2009, An association between tick bite reactions and red meat allergy in humans, Med J Aust, 190, 510, 10.5694/j.1326-5377.2009.tb02533.x · DOI
  5. Commins, 2009, Delayed anaphylaxis, angioedema, or urticaria after consumption of red meat in patients with IgE antibodies specific for galactose-alpha-1,3-galactose, J Allergy Clin Immunol, 123, 426, 10.1016/j.jaci.2008.10.052 · DOI
  6. O’Neil, 2007, High incidence of cetuximab-related infusion reactions in Tennessee and North Carolina and the association with atopic history, J Clin Oncol, 25, 3644, 10.1200/JCO.2007.11.7812 · DOI
  7. Chung, 2008, Cetuximab-induced anaphylaxis and IgE specific for galactose-α-1,3-galactose, N Engl J Med, 358, 1109, 10.1056/NEJMoa074943 · DOI · Paper page
  8. Qian, 2007, Structural characterization of N-linked oligosaccharides on monoclonal antibody cetuximab by the combination of orthogonal matrix-assisted laser desorption/ionization hybrid quadrupole-quadrupole time-of-flight tandem mass spectrometry and sequential enzy, Anal Biochem, 364, 8, 10.1016/j.ab.2007.01.023 · DOI
  9. Jacquenet, 2009, Mammalian meat-induced anaphylaxis: clinical relevance of anti-galactose-α-1,3-galactose IgE confirmed by means of skin tests to cetuximab, J Allergy Clin Immunol, 124, 603, 10.1016/j.jaci.2009.06.014 · DOI
  10. Apostolovic, 2016, The red meat allergy syndrome in Sweden, Allergo J, 25, 29, 10.1007/s15007-016-1044-7 · DOI
  11. Mabelane, 2018, Alpha gal allergy in rural black African subjects associated with a high prevalence of abdominal manifestations and a more rapid onset of symptoms, J Allergy Clin Immunol, 141, AB200, 10.1016/j.jaci.2017.12.633 · DOI
  12. Commins, 2016, Delayed anaphylaxis to alpha-gal, an oligosaccharide in mammalian meat, Allergol Int, 65, 16, 10.1016/j.alit.2015.10.001 · DOI
  13. Commins, 2011, The relevance of tick bites to the production of IgE antibodies to the mammalian oligosaccharide galactose-α-1,3-galactose, J Allergy Clin Immunol, 127, 1286, 10.1016/j.jaci.2011.02.019 · DOI · Paper page
  14. Fischer, 2017, Prevalence of type I sensitization to alpha-gal in forest service employees and hunters, Allergy, 72, 1540, 10.1111/all.13156 · DOI
  15. Venturini, 2018, IgE antibodies to alpha-gal in foresters and forest workers from La Rioja, North of Spain, J Investig Allergol Clin Immunol, 28, 106, 10.18176/jiaci.0218 · DOI
  16. Schmidle, 2019, Recall urticaria—a new clinical sign in the diagnosis of alpha-gal syndrome, J Allergy Clin Immunol Pract, 7, 685, 10.1016/j.jaip.2018.08.026 · DOI
  17. Hashizume, 2018, Repeated Amblyomma testudinarium tick bites are associated with increased galactose-α-1,3-galactose carbohydrate IgE antibody levels: a retrospective cohort study in a single institution, J Am Acad Dermatol, 78, 1135, 10.1016/j.jaad.2017.12.028 · DOI
  18. Hamsten, 2013, Identification of galactose-α-1,3-galactose in the gastrointestinal tract of the tick Ixodes ricinus: possible relationship with red meat allergy, Allergy, 68, 549, 10.1111/all.12128 · DOI
  19. Araujo, 2016, Amblyomma sculptum tick saliva: α-Gal identification, antibody response and possible association with red meat allergy in Brazil, Int J Parasitol, 46, 213, 10.1016/j.ijpara.2015.12.005 · DOI
  20. Chinuki, 2016, Haemaphysalis longicornis tick bites are a possible cause of red meat allergy in Japan, Allergy, 71, 421, 10.1111/all.12804 · DOI
  21. Cabezas-Cruz, 2018, Tick galactosyltransferases are involved in α-Gal synthesis and play a role during Anaplasma phagocytophilum infection and Ixodes scapularis tick vector development, Sci Rep, 8, 14224, 10.1038/s41598-018-32664-z · DOI
  22. Commins, 2017, Development of a novel murine model of alpha-gal meat allergy, J Allergy Clin Immunol, 139, AB193, 10.1016/j.jaci.2016.12.628 · DOI
  23. Tjernberg, 2017, IgE reactivity to α-Gal in relation to Lyme borreliosis, PLoS One, 12, e0185723, 10.1371/journal.pone.0185723 · DOI
  24. Wilson, 2017, Galactose-α-1,3-galactose: atypical food allergen or model IgE hypersensitivity?, Curr Allergy Asthma Rep, 17, 8, 10.1007/s11882-017-0672-7 · DOI
  25. Ohta, 2017, Skin CD4+memory T cells play an essential role in acquired anti-tick immunity through interleukin-3-mediated basophil recruitment to tick-feeding sites, Front Immunol, 8, 1348, 10.3389/fimmu.2017.01348 · DOI
  26. Arkestl, 2011, Impaired allergy diagnostics among parasite-infected patients caused by IgE antibodies to the carbohydrate epitope galactose-α1,3-galactose, J Allergy Clin Immunol, 127, 1024, 10.1016/j.jaci.2011.01.033 · DOI
  27. Mozzicato, 2014, Porcine or bovine valve replacement in 3 patients with IgE antibodies to the mammalian oligosaccharide galactose-alpha-1,3-galactose, J Allergy Clin Immunol Pract, 2, 637, 10.1016/j.jaip.2014.04.016 · DOI
  28. Stone, 2017, Anaphylaxis after zoster vaccine: Implicating alpha-gal allergy as a possible mechanism, J Allergy Clin Immunol, 10.1016/j.jaci.2016.10.037 · DOI
  29. Fischer, 2017, Alpha-gal is a possible target of IgE-mediated reactivity to antivenom, Allergy, 72, 764, 10.1111/all.13073 · DOI
  30. Apostolovic, 2014, Immunoproteomics of processed beef proteins reveal novel galactose-α-1,3-galactose-containing allergens, Allergy, 69, 1308, 10.1111/all.12462 · DOI
  31. Ristivojevic, 2018, alpha-Gal on the protein surface affects uptake and degradation in immature monocyte derived dendritic cells, Sci Rep, 8, 12684, 10.1038/s41598-018-30887-8 · DOI
  32. Caponetto, 2013, Gelatin-containing sweets can elicit anaphylaxis in a patient with sensitization to galactose-α-1,3-galactose, J Allergy Clin Immunol Pract, 1, 302, 10.1016/j.jaip.2013.01.007 · DOI
  33. Morisset, 2012, Anaphylaxis to pork kidney is related to IgE antibodies specific for galactose-alpha-1,3-galactose, Allergy, 67, 699, 10.1111/j.1398-9995.2012.02799.x · DOI
  34. Fischer, 2014, Galactose-alpha-1,3-galactose sensitization is a prerequisite for pork-kidney allergy and cofactor-related mammalian meat anaphylaxis, J Allergy Clin Immunol, 134, 755, 10.1016/j.jaci.2014.05.051 · DOI
  35. Fischer, 2016, Clinical spectrum of α-Gal syndrome: from immediate-type to delayed immediate-type reactions to mammalian innards and meat, Allergol J Int, 25, 55, 10.1007/s40629-016-0099-z · DOI
  36. Steinke, 2016, Altered metabolic profile in patients with IgE to galactose-alpha-1,3-galactose following in vivo food challenge, J Allergy Clin Immunol, 138, 1465, 10.1016/j.jaci.2016.05.021 · DOI
  37. Roenneberg, 2016, α-Gal-a new clue for anaphylaxis in mastocytosis, J Allergy Clin Immunol, 138, 1465
  38. Wölbing, 2013, About the role and underlying mechanisms of cofactors in anaphylaxis, Allergy, 68, 1085, 10.1111/all.12193 · DOI
  39. Commins, 2014, Delayed clinical and ex vivo response to mammalian meat in patients with IgE to galactose-alpha-1,3-galactose, J Allergy Clin Immunol, 134, 108, 10.1016/j.jaci.2014.01.024 · DOI
  40. Hamsten, 2013, Red meat allergy in Sweden: association with tick sensitization and B-negative blood groups, J Allergy Clin Immunol, 132, 1431, 10.1016/j.jaci.2013.07.050 · DOI
  41. Kennedy, 2013, Galactose-α-1,3-galactose and delayed anaphylaxis, angioedema, and urticaria in children, Pediatrics, 131, e1545, 10.1542/peds.2012-2585 · DOI
  42. Oostingh, 2003, Potential implications of ABO blood group for vascular rejection in pig to human kidney xenotransplantation, Xenotransplantation, 10, 278, 10.1034/j.1399-3089.2003.02060.x · DOI
  43. Rispens, 2013, IgE production to α-gal is accompanied by elevated levels of specific IgG1 antibodies and low amounts of IgE to blood group B, PLoS One, 8, e55566, 10.1371/journal.pone.0055566 · DOI
  44. Apostolovic, 2018, Immunoprofile of alpha-Gal- and B-antigen-specific responses differentiates red meat-allergic patients from healthy individuals, Allergy, 73, 1525, 10.1111/all.13400 · DOI
  45. Brestoff, 2018, The B antigen protects against the development of red meat allergy, J Allergy Clin Immunol Pract, 6, 1790, 10.1016/j.jaip.2018.02.010 · DOI
  46. Kollmann, 2017, The quantity and quality of α-gal-specific antibodies differ in individuals with and without delayed red meat allergy, Allergy, 72, 266, 10.1111/all.12948 · DOI
  47. Cabezas-Cruz, 2017, Effect of blood type on anti-a-Gal immunity and the incidence of infectious diseases, Exp Mol Med, 49, e301, 10.1038/emm.2016.164 · DOI
  48. Carter, 2018, Identification of alpha-gal sensitivity in patients with a diagnosis of idiopathic anaphylaxis, Allergy, 73, 1131, 10.1111/all.13366 · DOI
  49. Pattanaik, 2018, The changing face of anaphylaxis in adults and adolescents, Ann Allergy Asthma Immunol, 121, 594, 10.1016/j.anai.2018.07.017 · DOI
  50. Mateos-Hernández, 2017, Tick-host conflict: immunoglobulin E antibodies to tick proteins in patients with anaphylaxis to tick bite, Oncotarget, 8, 20630, 10.18632/oncotarget.15243 · DOI
  51. Gauci, 1989, Allergic reactions to the Australian paralysis tick, Ixodes holocyclus: diagnostic evaluation by skin test and radioimmunoassay, Clin Exp Allergy, 19, 279, 10.1111/j.1365-2222.1989.tb02384.x · DOI
  52. Van Wye, 1991, IgE antibodies in tick bite-induced anaphylaxis, J Allergy Clin Immunol, 88, 968, 10.1016/0091-6749(91)90257-O · DOI
  53. Molins, 2017, Metabolic differentiation of early Lyme disease from southern tick-associated rash illness (STARI), Sci Transl Med, 9, eaal2717, 10.1126/scitranslmed.aal2717 · DOI
  54. D’Alessandro, 2002, Alterations in serum anti-alpha-galactosyl antibodies in patients with Crohn’s disease and ulcerative colitis, Clin Immunol, 103, 63, 10.1006/clim.2001.5180 · DOI
  55. Mangold, 2011, Anti-Gal titers in healthy adults and inflammatory bowel disease patients, Transplant Proc, 43, 3964, 10.1016/j.transproceed.2011.09.074 · DOI
  56. Etienne-Decerf, 1987, Elevated anti-alpha-galactosyl antibody titres: a marker of progression in autoimmune thyroid disorders and in endocrine ophthalmopathy?, Acta Endocrinol (Copenh), 115, 67
  57. Wilson, 2018, IgE to the mammalian oligosaccharide galactose-alpha-1,3-galactose is associated with increased atheroma volume and plaques with unstable characteristics: brief report, Arterioscler Thromb Vasc Biol, 38, 1665, 10.1161/ATVBAHA.118.311222 · DOI
  58. Sun, 2007, Mast cells promote atherosclerosis by releasing proinflammatory cytokines, Nat Med, 13, 719, 10.1038/nm1601 · DOI

Cited by

Sorted by citations

See all 77

Metadata

Authors
Levin, M., Apostolovic, D., Biedermann, T., Commins, S. P., Iweala, O. I., Platts-Mills, T. A. E., Savi, E., van Hage, M., & Wilson, J. M.
Venue
Annals of Allergy, Asthma & Immunology
Publisher
Elsevier BV
Published
2019-06
Volume
122
Issue
6
Pages
598-602
ISSN
1081-1206
DOI
10.1016/j.anai.2019.03.021
PMC
PMC6839685
Cited by
77
References
1
Language
en
Licence

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Galactose α-1,3-galactose phenotypes. https://app.cochat.ai/papers/10.1016/j.anai.2019.03.021
The paper
Levin, M., Apostolovic, D., Biedermann, T., Commins, S. P., Iweala, O. I., Platts-Mills, T. A. E., Savi, E., van Hage, M., & Wilson, J. M. (2019). Galactose α-1,3-galactose phenotypes. Annals of Allergy, Asthma & Immunology. https://doi.org/10.1016/j.anai.2019.03.021