Mg. Karlsson et al., NASAL MESSENGER-RNA EXPRESSION OF INTERLEUKIN-2, INTERLEUKIN-4, AND INTERLEUKIN-5 IN PATIENTS WITH ALLERGIC RHINITIS, Diagnostic molecular pathology, 4(2), 1995, pp. 85-92
In nasal biopsies from 17 adult patients with seasonal allergic rhinit
is and from 10 healthy controls, cytokines were analyzed by reverse-tr
anscriptase polymerase chain reaction (RT-PCR), The time-course study
during winter included repeated local allergen provocation with subseq
uent nasal biopsies as well as biopsies taken during pollen season. Th
e RT-PCR for CD44 yielded positive bands in 65 of 71 cases, in which c
ases mRNA for interleukins 2, 4, and 5 (IL-2, IL-4, and IL-5) were thu
s investigated by means of seminested PCR. IL-4 mRNA was found almost
exclusively in the allergic patients. During provocation a significant
increase in IL-4 was noticed compared with controls (p = 0.043). Equa
lly, during the natural pollen season, IL-4 mRNA expression was signif
icantly higher in patients not using nasal corticosteroids compared wi
th those who did (p = 0.011). No differences in IL-2 or IL-5 were obse
rved between the groups. These findings also indicate, together with e
arlier observations of T-cell activation, a phenotype switch toward T-
helper 2 (Th2) cells, and the accumulation (homing) of these T cells i
n the nasal mucosa, that T cells constitute the main source for IL-4 i
n the nasal mucosa. Therefore, allergic patients have an increased syn
thesis of IL-4 when provoked with the allergen, and during natural pol
len season this synthesis can be downregulated by corticosteroids. Fur
thermore, this study exemplifies the versatility of molecular biology
in surgical pathology and that even low-copy-number cytokine mRNA can
be examined in routinely snap-frozen surgical specimens.