Models of filarial infection in laboratory inbred mice are valuable to
ols for assessing the relevance of antifilarial immune responses in pr
otection against these parasites. However, laboratory mice are not per
missive for those filarial species which are known to infect humans. T
herefore, immunity to the different stages of these filariae, i.e. inf
ective third stage larvae (L3), adults and microfilariae, has been ana
lyzed separately, as a surrogate approach. Although much information h
as been gathered by analysis of immunity and intervention in particula
r immune responses in these experimental systems, interference of diff
erent stage-specific responses as well as modulation of filarial matur
ation by the immune system cannot be assessed. A newly established inf
ection model of filariasis, namely infection of laboratory mice with L
itomosoides sigmodontis, accommodates the full developmental cycle of
the parasite and may overcome this deficiency. Although the disadvanta
ge of this latter model is that it deals with a filaria which is not p
athogenic to man, it is the only model in which immunity can be analyz
ed during maturation of infective larvae into adult worms, the period
considered most important for vaccination studies.