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2021 中国共识文件:过敏原诊断(英文)

作者:中华医学网发布时间:2026-01-20 20:01浏览:

2021《China Consensus Document on Allergy Diagnostics》(AAIR,2021;DOI:10.4168/aair.2021.13.2.177)由中国多学会联合制定,是国内首部过敏性疾病病因诊断指南,聚焦 IgE 介导机制,规范体内外检测路径、组分诊断与临床决策,适配中国过敏原分布特征PubMed。以下为结构化英文要点解读。
 

 

一、Basic Principles & Diagnostic Algorithm

 
  1. Core Purpose
    • Standardize in vivo/in vitro testing, clarify cross-sensitization/co-sensitization interpretation, and integrate clinical history with test results for etiological diagnosisPubMed.
     
  2. Diagnostic Workflow
    1. Clinical assessment: History (symptom pattern, exposure triggers, comorbidities)+physical examination (mucosal edema, wheezing, skin rash).
    2. Initial screening: Skin prick test (SPT) or serum specific IgE (sIgE) → positive = IgE-mediated allergy.
    3. Local allergy evaluation: If SPT/sIgE negative, test local secretions (nasal/bronchial) sIgE → positive = local allergic rhinitis/asthma.
    4. Definitive confirmation: Allergen provocation test or elimination-challenge if above negative but clinically suspected.
     
 

 

二、In Vivo Testing (Core In Vivo Methods)

 
Test Indications Procedure Result Interpretation Strengths/Limitations
SPT Initial screening for inhalant/food allergens 20-30 min after pricking, measure wheal ≥3 mm vs. negative control ≥3 mm = positive; fresh food SPT for fruit/vegetable allergy Fast, cost-effective; contraindicated in severe skin disease/antihistamine use
Intradermal test Low SPT reactivity, drug allergy 0.01-0.02 mL allergen injected intradermally, read at 15-20 min Wheal ≥5 mm = positive High sensitivity; higher false-positive rate, risk of systemic reaction
Allergen provocation test (nasal/bronchial/oral) Refractory cases, local allergy confirmation Controlled exposure to allergen, monitor symptoms/signs Positive if symptoms reproduce with objective markers Gold standard for local allergy; requires experienced team, risk of severe reaction
 

 

三、In Vitro Testing (Key Laboratory Tools)

 
Assay Target Clinical Value Cut-off/Interpretation Notes
Serum sIgE Allergen-specific IgE Identify sensitization; predict reaction severity Class 0: <0.35 kUA/L (negative); Class 1-6: ≥0.35 kUA/L (positive, higher class = higher reactivity) Widely available; unaffected by antihistamines; cannot distinguish active allergy from sensitization
Component-resolved diagnosis (CRD) Allergen components (e.g., Der p 1/Der p 2, Phl p 1/5) Differentiate cross-sensitization (e.g., birch-pollen-food syndrome), predict severe reaction risk Component sIgE positive indicates true sensitization vs. cross-reactivity Critical for immunotherapy candidate selection; costlier, limited component availability
Basophil activation test (BAT) CD63/CD203c expression on basophils Diagnose drug allergy, severe anaphylaxis; monitor immunotherapy response Activation rate ≥15% = positive High specificity; requires fresh blood, technical expertise
Total IgE Total serum IgE level Screen atopy; not diagnostic alone Normal range varies by age/laboratory Elevated in atopy but non-specific
 

 

四、Allergen Spectrum & Regional Distribution (China-Specific)

 
  1. Inhalant Allergens
    • Northern China: Dust mites (Der p/f), Artemisia, Humulus japonicus, birch pollen.
    • Southern China: Dust mites, mold (Aspergillus/Cladosporium), cockroach, ragweedPubMed.
     
  2. Food Allergens
    • Common: Cow’s milk, egg, peanut, shrimp, wheat.
    • Regional: Mango (Southern), peach (Northern), buckwheat (some areas).
     
  3. Cross-Sensitization Patterns
    • Pollen-food syndrome: Birch pollen (Bet v 1) cross-reacts with apple/peach; mugwort (Art v 1) with celery/carrot.
    • Dust mite-cockroach: Tropomyosin cross-reactivity.
     
 

 

五、Special Populations & Clinical Pearls

 
  1. Children
    • SPT preferred for ≥3 years; serum sIgE for <3 years or antihistamine use.
    • CRD helps distinguish true food allergy from cross-sensitization.
     
  2. Pregnancy/Lactation
    • SPT/intradermal test avoided in first trimester; serum sIgE safe.
     
  3. Elderly
    • Consider polypharmacy (e.g., beta-blockers) affecting test results; lower skin reactivity may require intradermal test.
     
  4. Common Pitfalls
    • Over-reliance on sIgE class without clinical correlation (sensitization ≠ allergy).
    • Neglecting local allergy (normal serum sIgE but positive local secretion sIgE).
    • Misinterpreting cross-sensitization as true allergy (CRD essential).
     
 

 

六、Core Recommendations

 
  1. Diagnosis
    • Prioritize clinical history + SPT/serum sIgE as first-line screening.
    • Use CRD for cross-sensitization differentiation and immunotherapy candidate selection.
    • Allergen provocation test reserved for refractory/local allergy cases.
     
  2. Testing Standardization
    • SPT: Use standardized extracts, avoid antihistamines 3-7 days prior.
    • Serum sIgE: Follow manufacturer cut-offs; results should be laboratory-commutable.
     
  3. Result Interpretation
    • Combine test results with symptoms, exposure history, and response to avoidance/medication.