A. Vigano et al., ELEVATION OF IGE IN HIV-INFECTED CHILDREN AND ITS CORRELATION WITH THE PROGRESSION OF DISEASE, Journal of allergy and clinical immunology, 95(2), 1995, pp. 627-632
Background: According to recent data, a switch from a T-H1 to a T-H2 p
attern of cytokines might be a critical step in the progression of hum
an immunodeficiency virus (HN) infection. Previous studies have demons
trated a disturbance in IgE synthesis in HIV-infected adults. Methods:
Fifty-eight children infected vertically with HN and 35 children with
seroreversion, aged 4 months to 11 years, were evaluated for IgE seru
m level, CD4(+) cell count, skin prick test responses to common airbor
ne and food allergens individual and family history of atopy, and pres
ence of opportunistic infections. In thirty of the 58 HIV-infected chi
ldren serum interleukin-4 and interferon-gamma levels were assessed. T
hirty-three of the 58 HIV-infected children had a follow-up of 1 year
for IgE levels, CD4(+) cell count, and occurrence of opportunistic inf
ections and recurrent bacterial infections. Results: Both IgE concentr
ation and the percentage of children with IgE elevation were markedly
increased (with no correlation to skin prick test responses or opportu
nistic infections) in the group of 58 HIV-infected children as compare
d with the 35 children with seroreversion (p < 0.05). The same paramet
ers were higher in children with acquired immunodeficiency syndrome as
compared with children with asymptomatic or mildly symptomatic diseas
e (p < 0.05). Serum interleukin-4 and interferon-gamma levels do not a
ccount for IgE hyperproduction. There was a significant association be
tween persistent IgE elevation and severe decline (greater than or equ
al to 30% over 1 year) in CD4(+) counts, as well as increased suscepti
bility to bacterial infections. Conclusions: Our study demonstrates a
spectrum of IgE dysfunction in children, which is similar to that obse
rved in adults. A persistent IgE hyperproduction appears to be associa
ted with a severe decline in CD4(+) cell count, suggesting that this c
linical test is a useful marker of disease progression.