Wa. Nish et al., THE EFFECT OF IMMUNOTHERAPY ON THE CUTANEOUS LATE-PHASE RESPONSE TO ANTIGEN, Journal of allergy and clinical immunology, 93(2), 1994, pp. 484-493
Background: This study used the skin chamber model to evaluate prospec
tively the effect of immunotherapy (IT) on the cutaneous early and lat
e phase response (LPR) to epicutaneous antigen challenge. Methods: Nin
e subjects with allergic rhinitis were studied at three time points: b
efore starting IT, after 3 months of IT, and after 6 months of IT. Ski
n chamber histamine content was measured hourly for it hours, and cell
counts performed hourly during hours 6 to 12. An intradermal skin tes
t was placed, and the reaction was measured hourly for 12 hours. Skin
biopsy specimens were obtained 8 hours after intradermal placement and
evaluated for cellular infiltrate and major basic protein deposition.
Serum antigen-specific IgG and IgE levels were measured at each time
point to confirm physiologic effect of IT. Results: Six months of IT s
ignificantly (p < 0.05) decreased both early and LPR shin test reactiv
ity and skin chamber histamine for hours 1 to 3, 4 to 6, and 9 to 12.
Skin chamber LPR cellular influx decreased significantly (p < 0.05) fo
r neutrophils only. Decrease in LPR histamine after 6 months of IT was
significantly correlated with both decrease in mononuclear cells (R(2
) = 0.817, p = 0.002) and decrease in neutrophils (R(2) = 0.813, p = 0
.009). Also significantly correlated were decrease in LPR skin test re
activity, with percent change in skin chamber mononuclear cells (R(2)
= 0.800, p = 0.009) and decrease in early skin test reactivity (R(2) =
0.675, p = 0.01). Biopsy specimens showed no consistent change in eit
her dermal cellular infiltrate or deposition of major basic protein. C
onclusion: IT significantly attenuates cutaneous histamine release and
skin test reactivity and is accompanied by a decrease in skin chamber
LPR neutrophil influx without significantly altering the dermal infil
trate at 8 hours.