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*
Department of Pathology, University of Connecticut Health Center, Farmington, CT 06030;
Department of Biology, Louisiana State University, Baton Rouge, LA 70803; and
The Jackson Laboratory, Bar Harbor, ME 04609
Human lymphatic filariasis, which afflicts an estimated 120 million
people worldwide, is caused by the large nematode parasites
Wuchereria bancrofti and Brugia malayi.
Filarial nematodes require both an arthropod vector and a mammalian
host to complete their life cycle. Within the definitive (mammalian)
host, the lymphatic filarial parasites reside in the lymph nodes and
lymphatics, a seemingly hostile environment for infectious agents,
since the location exposes them to the immune defenses of the host. We
present data here that suggest that the growth of B.
malayi in the mammalian host is dependent on host NK cell
function. Comparisons of worm survival and development in different
strains of mice with varying levels of NK cell activity reveal that
NOD/LtSz-scid/scid and NOD/LtSz-scid/scid
B2mnull mice (with diminished to absent NK cell activity
respectively), are nonpermissive to worm growth, while
C.B-17-scid/scid mice with normal NK cell activity are
highly permissive. Depletion of NK cells in the permissive
C57BL/6J-scid/scid mice renders them nonpermissive to
B. malayi growth, whereas stimulation of NK cells in
NOD/LtSz-scid/scid mice makes them permissive. Tg
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mice, which lack NK and T cells, are nonpermissive, but, when
reconstituted with NK cells by adoptive transfer of bone marrow cells
from C57BL/6J-scid/scid mice, are rendered permissive.
This requirement for NK cell activity may explain the site specificity
of these parasites. Furthermore, these data suggest that the
interaction of the host immune system with the filarial parasite is
double edged, with both host protective and parasite growth-promoting
activities emanating from the former.
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