1.Basophil Markers for Identification and Activation in the Indirect Basophil Activation Test by Flow Cytometry for Diagnosis of Autoimmune Urticaria.
Zehwan KIM ; Bong Seok CHOI ; Jong Kun KIM ; Dong Il WON
Annals of Laboratory Medicine 2016;36(1):28-35
BACKGROUND: The indirect basophil activation test using flow cytometry is a promising tool for autoimmune urticaria diagnosis. We aimed to identify better donor basophils (from atopic vs. non-atopic donors and interleukin-3 primed vs. unprimed basophils) and improve basophil identification and activation markers (eotaxin CC chemokine receptor-3 [CCR3] vs. CD123 and CD63 vs. CD203c). METHODS: Donor basophils were obtained from non-atopic and atopic group O donors. Positive control sera were artificially prepared to simulate autoimmune urticaria patients' sera. Patient sera were obtained from nine children with chronic urticaria. Assay sensitivity was compared among each variation by using positive control sera (n=21), applying cutoff values defined from negative control sera (n=20). RESULTS: For basophil identification, a combination of CCR3 and CD123 markers revealed a higher correlation with automated complete blood count (r=0.530) compared with that observed using CD123 (r=0.498) or CCR3 alone (r=0.195). Three activation markers on the atopic donor basophils attained 100% assay sensitivity: CD203c on unprimed basophils, CD63+CD203+ or CD63 alone on primed basophils; however, these markers on the non-atopic donor basophils attained lower assay sensitivity. CONCLUSIONS: For basophil identification markers, a combination of CD123 and CCR3 is recommended, while CD123 alone may be used as an alternative. Donor basophils should be obtained from an atopic donor. For basophil activation markers, either CD203c alone on unprimed basophils or CD203c and CD63 on primed basophils are recommended, while CD63 alone on primed basophils may be used as an alternative.
Autoimmune Diseases/blood/*diagnosis/immunology
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Basophils/*immunology/metabolism
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Biomarkers/blood
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Child
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Flow Cytometry
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Humans
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Interleukin-3 Receptor alpha Subunit/blood
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Male
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Receptors, CCR3/blood
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Urticaria/blood/*diagnosis/immunology
2.Basophil Activation Test for Chronic Urticaria.
Annals of Laboratory Medicine 2016;36(5):499-500
No abstract available.
Basophils/cytology/*metabolism
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Flow Cytometry
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HLA-DR Antigens/metabolism
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Humans
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Interleukin-3 Receptor alpha Subunit/metabolism
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Leukocyte Count
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Phosphoric Diester Hydrolases/metabolism
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Pyrophosphatases/metabolism
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Receptors, CCR3/metabolism
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Urticaria/*diagnosis/immunology/metabolism
3.Immunologic Evaluation of Immediate Hypersensitivity to Cefaclor.
Hye Soo YOO ; Seung Hyun KIM ; Hyouk Soo KWON ; Tae Bum KIM ; Young Hee NAM ; Young Min YE ; Hae Sim PARK
Yonsei Medical Journal 2014;55(6):1473-1483
PURPOSE: Cefaclor is widely prescribed for various infectious diseases. As its consumption increases, the number of hypersensitivity reactions to cefaclor has increased. This study aimed to evaluate the immunologic findings of immediate hypersensitivity to cefaclor. MATERIALS AND METHODS: We enrolled 47 patients with immediate hypersensitivity to cefaclor from Ajou University Hospital and Asan Medical Center. Serum specific IgE, IgG1, and IgG4 antibodies to cefaclor-human serum albumin (HSA) conjugate were measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: The most common phenotype was anaphylaxis (Group I, 78.7%), followed by urticaria (Group II, 21.3%). The detection of specific IgE, IgG1, and IgG4 to cefaclor-HSA conjugate by ELISA tended to be higher in Group I (40.5%, 41.7%, 21.6%) than in Group II (20.0%, 20.0%, 0%) with no statistical significance. Significant associations were found between specific IgE and IgG1 or IgG4 (p<0.001, p=0.019). ELISA inhibition tests showed significant inhibitions by both free cefaclor and cefaclor-HSA conjugate. For basophil activation tests in patients having no specific IgE antibody, the CD63 expression level on basophils increased with incubations of free cefaclor. CONCLUSION: The most common manifestation of immediate hypersensitivity to cefaclor was anaphylaxis, most of which was mediated by IgE; however, a non-IgE mediated direct basophil activation mechanism was suggested in a subset of anaphylaxis patients.
Adolescent
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Adult
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Aged
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Anaphylaxis/*chemically induced/immunology
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Anti-Bacterial Agents/adverse effects/*immunology
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Antigens, CD63
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Basophils/metabolism
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Cefaclor/*adverse effects/immunology
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Enzyme-Linked Immunosorbent Assay
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Female
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Humans
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Hypersensitivity, Immediate/chemically induced/diagnosis/*immunology
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Immunoglobulin E/*blood
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Immunoglobulin G/immunology
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Male
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Middle Aged
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Retrospective Studies
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Skin Tests
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Urticaria/chemically induced/diagnosis/immunology
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Young Adult