Ml. Cross et al., MODULATION OF MURINE CELLULAR IMMUNE-RESPONSES AND CYTOKINES BY SALIVARY-GLAND EXTRACT OF THE BLACK FLY SIMULIUM-VITTATUM, Tropical medicine and parasitology, 45(2), 1994, pp. 119-124
Salivary gland extract (SGE) of the blood-feeding black fly Simulium v
ittatum is known to modulate immunological responses. In the present s
tudy, the ability of S. vittatum SGE to modulate responses during hete
rologous antigenic challenge was investigated in a murine model, with
particular emphasis on characterizing the patterns of cytokine respons
e. Mice were injected repeatedly with SGE or saline (sham), then chall
enged with the T dependent antigen ovalbumin (OVA) to generate antigen
-specific lymphoblasts. Spleen cells from OVA-primed mice were then co
-cultured with OVA in vitro to stimulate cytokine secretion. Cells fro
m mice that had been injected with SGE prior to OVA challenge produced
lower levels of interleukins 5 and 10 (IL-5 and IL-10) in in vitro cu
lture, when stimulated with OVA, compared to mice that had been sham-i
njected with saline. Levels of IFN-gamma IL-2 and IL-4 did not differ
significantly between SGE- and saline-injected groups. Mice injected r
epeatedly with SGE prior to OVA challenge had fewer circulating eosino
phils than sham-injected mice, while other leukocyte levels were unaff
ected by SGE. Prior exposure to SGE did not affect levels of serum IgE
or IgA significantly. The effect of SGE on the ability of murine sple
en cells to respond in vitro to the recombinant cytokines IL-2 and IL-
4 was also investigated. Naive spleen cells pre-incubated with SGE pro
liferated less in response to both IL-2 and IL-4 in in vitro culture t
han cells pre-incubated with saline as a control. Residual levels of I
L-4 were higher in culture supernatants of SGE-treated cells following
cytokine stimulation, suggesting that SGE had inhibited the cells' ab
ility to utilize exogenous IL-4. This report emphasizes that immunolog
ical studies of vector-borne diseases should not overlook the importan
t contribution of the vector to host immunocompetence. Results are dis
cussed with particular emphasis on the use of murine models in studies
of onchocerciasis.