The current unfavourable trends in asthma and atopy prevalences have raised
great concern and have challenged investigators to accelerate search for n
ew risk factors for atopic diseases. The lack or scarcity of intense, syste
mic infections in early life has been postulated to increase susceptibility
of becoming sensitized to otherwise harmless allergens in later life. This
hygiene hypothesis is considered one of the most plausible explanations fo
r the current trends in atopic diseases to date. There are data to suggest
that measles, hepatitis A, and Mycobacterium tuberculosis infection in earl
y life may prevent the subsequent development of atopic diseases. The hypot
hesis is based on the concept that certain viral and bacterial infections,
which induce a strongly polarized T helper (Th)-1 type response and a long-
lasting memory immunity, are in early life able to reverse or prevent the b
iased Th1/Th2 balance in individuals prone to atopy and asthma. Evidence fo
r the ability of mycobacterial infections to alter the Th1/Th2 balance has
also been obtained from murine models. In humans, the critical time period
during which immunomodulation with long-lasting effects is considered most
successful is within the first two years of life. Possibly also nonpathogen
ic residents of the intestinal mucosa are involved in the proper maturation
of the immune system. The use of antibiotics has been shown to be positive
ly associated with the development of asthma and atopy. The mechanisms unde
rlying these associations remain largely unknown.