Eosinophilic granulocytes have been implicated as possible effector cells in host resistance to Trypanosoma cruzi infection. Eosinophils have been found in the parasite-containing lesions of hosts with acute Chagas' disease (Koberle, 1968, Adv. Parasit. (B. Dawes, ed.) 6: 63-110) and are thought to function as the cellular component of an antibody dependent cellular cytotoxicity (ADCC) response against the parasite. Indeed, eosinophils from man (Kierszenbaum, 1979, Am. J. trop. Med. Hyg. 28: 965-968) and rodents (Sanderson et al., 1977, Nature, Lond. 268: 340341; Kipnis et al., 1981, Am. J. trop. Med. Hyg. 30: 47-53) have been shown capable of destroying trypanosomes by ADCC in the presence of immune serum. If eosinophils play a role in host protection against T. cruzi, the dynamics of this cell type during infection becomes an important consideration. To evaluate eosinophil levels through T. cruzi infection, the bone marrows of 8 wk old C3H(He) (Dominion Labs, Dublin, VA) and C57B1/6 (Jackson Labs, Bar Harbor, ME) female mice infected intraperitoneally with 1 x 103 Brazil strain trypomastigotes were assayed by 2 methods. One technique involved removal of the left femur from mice asphyxiated with CO2 and flushing the marrow with 1.0 ml of Alsever's solution (femoral bone marrow wash; FBMW). The resulting cell suspension was examined microscopically by standard hemocytometer methods for the total nucleated cell count by Turk's stain and the number of eosinophils using Discombe's stain (Discombe, 1946, Lancet 1, pp. 195-196). Discombe's stain (8 parts dH2O, 1 part 3% eosin Y and 1 part acetone) was incubated for 5 min at a 1 part cell suspension to 10 parts stain ratio prior to counting. The level of eosinophils for each animal was estimated as follows: % eosinophils = (# eosinophils per ml FBMW/# of nucleated cells per ml FBMW) x 100. Eosinophil percent data were normalized by the arcsin transformation before statistical analysis using ANOVA and Duncan's statistical tests (Zar, 1974. Biostatistical analysis. PrenticeHall, Inc., Englewood Cliffs, NJ). Parasitemia determination was done by microscopic examination of 4 ul of tail vein blood under an 18 mm circular coverslip (Kuhn et al., 1975, Int. J. Parasit. 5: 557-560). C3H(He) mice, on days 7, 14, 21, and 28 of acute infection, and C57B1/6 mice, on days 14, 28, and 42 of acute infection and day 90 representing post-acute infection, were sacrificed and
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