Evaluation of IFN-γ Enzyme-linked Immunospot Assay (ELISPOT) as a First-line Test in the Diagnosis of Non-Immediate Hypersensitivity to Amoxicillin and Penicillin
Language English Country Czech Republic Media print
Document type Journal Article, Observational Study
Grant support
00023884
Ministerstvo Zdravotnictví Ceské Republiky
IG144102
Ministerstvo Zdravotnictví Ceské Republiky
PubMed
29665345
DOI
10.14712/23362936.2018.3
PII: pmr_2018119010030
Knihovny.cz E-resources
- Keywords
- Allergy, Amoxicillin, ELISPOT, Hypersensitivity, Penicillin,
- MeSH
- Amoxicillin adverse effects immunology MeSH
- Anti-Bacterial Agents adverse effects immunology MeSH
- Adult MeSH
- Enzyme-Linked Immunospot Assay methods MeSH
- Immunoenzyme Techniques MeSH
- Drug Hypersensitivity diagnosis immunology MeSH
- Middle Aged MeSH
- Humans MeSH
- Penicillins adverse effects immunology MeSH
- Prospective Studies MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Observational Study MeSH
- Names of Substances
- Amoxicillin MeSH
- Anti-Bacterial Agents MeSH
- Penicillins MeSH
The current diagnostic algorithm for beta-lactam allergy is based on skin and provocation tests, both of which carry a certain risk of inducing hypersensitivity reactions. Thus, non-invasive in vitro tests reliable enough to replace skin and provocation tests at least in a portion of patients are desirable. We aimed to verify the utility of IFN-γ ELISPOT as a first-line test in patients with suspected non-immediate hypersensitivity reaction to amoxicillin (AMX) and penicillin (PNC). The prospective observational study included 24 patients with recent, suspected non-immediate hypersensitivity reaction to AMX or PNC and 6 recently-exposed healthy subjects. In vitro tests were performed in all patients and healthy subjects: a) IFN-γ ELISPOT with PNC, AMX and amoxicillin plus clavulanic acid (AMX-CL); b) penicillin specific IgE; c) basophil activation test (BAT). Skin and provocation tests followed only in certain patients. IFN-γ ELISPOT results with PNC and AMX stimulation did not differ from the unstimulated condition. The highest IFN-γ responses to AMX-CL were close to previously published criteria in three patients; one of which had true hypersensitivity according to drug provocation tests. Five patients with confirmed hypersensitivity by skin tests showed no response to the culprit antibiotic on IFN-γ ELISPOT assay. Our results did not support the utility of IFN-γ ELISPOT in the diagnosis of mild, non-immediate hypersensitivity to amoxicillin and penicillin.
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