Lg. Arlian et al., RESISTANCE AND IMMUNE-RESPONSE IN SCABIES-INFESTED HOSTS IMMUNIZED WITH DERMATOPHAGOIDES MITES, The American journal of tropical medicine and hygiene, 52(6), 1995, pp. 539-545
Citations number
40
Categorie Soggetti
Public, Environmental & Occupation Heath","Tropical Medicine
Seventy-one percent of rabbits immunized with a mixed (50:50) Dermatop
hagoides farinae and D. pteronyssinus house dust mite extract were res
istant to infestation by Sarcoptes scabiei var. canis. The resistance
was evidenced by a marked reduction in parasite load. All immunized ho
sts developed similar immunogen-specific antibody titers that were ind
ependent of the levels of scabies infestation that developed when the
hosts were infested with scabies. Resistant hosts exhibited significan
tly lower scabies-specific immunoglobulin titers and produced antibody
to fewer scabies antigens than did nonresistant hosts. All infested h
osts (resistant and nonresistant) showed a cellular infiltrate in the
scabietic lesions that was composed of neutrophils, plasma cells, macr
ophages, and mononuclear cell. Resistant hosts were characterized by f
ewer plasma cells in the infiltrate than were observed for non-resista
nt hosts. Resistant hosts exhibited a gradual increase in the number o
f infiltrating neutrophils, followed by a decrease that correlated wit
h a decrease in the mite burden. Nonresistant hosts exhibited an early
rapid increase, a decrease, and then a gradual increase in the concen
tration of neutrophils as the mite load increased. These results clear
ly showed that D. farinae/D. pteronyssinus antigens/epitopes can sensi
tize the hosts to scabies mites and induce protective immunity. The lo
wer circulating antibody levels and generally stronger inflammatory ce
ll-mediated response of resistant hosts compared with nonresistant hos
ts suggested that the mechanism by which immunization with Dermatophag
oides mites induces immunity to scabies mites involved a down-regulate
d T helper cell type 2 (Th2) response with reduced antibody production
but an up-regulated and stronger Th1 (inflammatory cell-mediated) res
ponse to scabies.