This month, Rondón et al. (J Allergy Clin Immunol 2012;129:1460-1467)
present an important classificatory revision centered on their identification
of a new rhinitis phenotype: local allergic rhinitis (LAR). Building on their
previous research, the authors characterize LAR as local specific IgE (sIgE), TH2
local tissue response, and positive nasal allergen provocation test (NAPT)
results in the absence of clinical indicators of systemic atopy, such as positive
skin tests and serum specific-IgE. Patients with LAR are known to respond
positively to nasal corticosteroids. In addition, they note that conjunctivitis
and/or asthma can be comorbid with LAR.
Rondón et al. effectively argue that the
current allergic versus non-allergic rhinitis (AR and NAR, respectively) distinction
is not sufficient in light of the findings of localized atopy. They suggest
that patients diagnosed with idiopathic rhinitis or non-allergic rhinitis with
eosinophilia may in fact have LAR, which would decisively impact clinical
management as patients with true idiopathic or non-allergic (vasomotor)
rhinitis would not respond to therapy like LAR patients would.
The authors propose a revised rhinitis
classification (Table 1, pp#) that splits allergic rhinitis into systemic and
local atopy subcategories. They estimate prevalence from European data to be
between 47-62% of patients reporting seasonal or perennial allergy symptoms. Their
and other early results have shown that house dust mite, grass, and olive
pollen are common triggers, though they note that comprehensive findings are
needed to refine NAPT specificity.
Rondón et al. review the published
pathophysiology evidence as well as the reported clinical presentation. They clearly
identify the gaps that future research should fill, such as clinical management
overlap between AR and LAR, the need for more practical NAPT testing
procedures, the relationship between LAR and atopic march, and mechanisms of
localized allergic responses. The authors comment that patients with LAR
receiving subcutaneous immunotherapy have increased tolerance upon repeat NAPT
and also develop positive skin tests and detectable serum specific-IgE.
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