Current issues relating to in vitro testing for
allergen-specific IgE: a workshop repotr
Annals of Allergy, Asthma, and Immunology;
May 1999
Purpose of Workshop
To discuss the current status of in vitro testing for allergen-specific
IgE and to examine various applications of this technology in routine
clinical practice. Workshop panelists consisted of a distinguished
group of physicians and scientists and known thought leaders in
the areas of allergy and immunology. Combined, this auspicious
group has published 792 articles in this field.
Use of IgE in Clinical Practice
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Patient history is not enough for specific allergen identification,
which is necessary for appropriate treatment.
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Well standardized
in vitro tests are an alternative to skin testing and there
are special situations where in vitro testing may be preferable
or specifically indicated.
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Every physician who is seeing a suspected allergic patient
should consider testing for allergen specific IgE to identify
the specific cause.
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In vitro testing by generalist physicians (family practitioners,
internists, pediatricians) is appropriate to effectively
manage and properly refer patients. They suggest initial screening
with a basic panel based on patient history.
In vitro (Blood) Testing vs.
Skin Testing
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NIH guidelines
for asthma recommend either in vivo or in vitro to identify
specific allergen sensitivities.
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"Compared with skin testing, in vitro testing may be easier to standardize and performance characteristics
can be defined."
Comparison of in vitro Technology
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Results from proficiency
testing surveys suggest that not all in vitro tests for IgE
perform equally well; further, they acknowledged that
in vitro
technology has significantly advanced since its inception.
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Specific
IgE Assay Calibrators should be standardized against the
WHO Reference Preparation for IgE for true quantitative results.
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