Measles is one of the major causes of childhood mortality in developin
g countries, despite current prevention of over 2 million child deaths
each year by measles vaccination programmes. New strategies, such as
mass campaigns, and possibly new preparations oi measles vaccines, may
facilitate further progress in controlling the disease and improving
the prospects for its ultimate eradication. To evaluate the potential
for non-percutaneous routes oi vaccine administration to improve contr
ol, we reviewed studies of serological responses to measles vaccine af
ter intradermal, conjunctival, oral, aerosol and intranasal administra
tion. The response to intradermal vaccination exceeded percutaneous re
sults in only one of eight instances in live studies where such compar
isons could be made, often producing substantially lower seroresponses
. Further, intradermal administration using a needle and syringe is mo
re difficult than subcutaneous vaccination. Alter oral administration
of vaccine, less than 50% of children seroconverted in three small stu
dies. Intranasal administration has not been studied extensively, but
it may be susceptible to interference by upper respiratory infections.
Seroconversion after conjunctival administration was very variable, a
nd this route was difficult practically in young children. In infants
below 9 months oi age, aerosol administration of vaccine resulted in 8
0% or better seroresponse in seven of nine trials, with the Edmonston-
Zagreb strain in standard titre doses consistently producing better re
sults than the Schwarz strain. However, seroresponses after subcutaneo
us administration clearly exceeded those from aerosols oi the same vac
cine in four of six comparisons. Several trials noted practical diffic
ulties in aerosol administration in young infants. in contrast, older
seronegative children generally responded well to aerosol administrati
on oi vaccine (above 90% and often 100% seroresponse), regardless of v
accine strain and often with surprisingly low estimated retained doses
. In each of three studies where it was possible to compare the same v
accines given percutaneously and by aerosol to seropositive children,
better seroresponses followed aerosols. In older children, aerosols of
the Edmonston-Zagreb strain also rather consistently provided better
seroresponses than aerosols of the Schwarz strain, with the most notab
le differences in seropositive children. Thus; with the possible excep
tion of very young infants, the aerosol route is promising and offers
several theoretical and practical advantages as well. Further randomiz
ed trials should be conducted to evaluate comparative responses to aer
osolized, intranasal, and subcutaneous vaccine, especially in those ag
e ranges targeted for mass campaigns (most commonly 9 months to 15 yea
rs). The development oi improved technology for aerosol delivery of me
asles vaccine would greatly advance the potential for wide scale use o
i this route, especially in mass campaigns in low income countries. (C
) 1997 The international Association of Biological Standardization.