Eosinophils are components of inflammatory responses to a variety of p
athogens. Although a variety of beneficial and harmful functions have
been ascribed to these cells, their role in protection against infecti
ous agents remains uncertain. Previous studies have reported eosinophi
lic pneumonia in mice infected intratracheally with Cryptococcus neofo
rmans. We confirmed this observation and studied the inflammatory resp
onse in the lung at day 14 by light and electron microscopy. Immunosta
ining for glucuronoxylomannan showed isolated cryptococci inside the e
osinophilic cuffs. Eosinophils were found to be in close association w
ith C. neoformans in vivo. Cryptococci were associated with eosinophil
s within eosinophilic perivascular cuffs, within granulomas, and linin
g the alveolar space, To further investigate this phenomenon in vitro,
we isolated rat peritoneal eosinophils and studied cryptococcus-eosin
ophil interactions in the presence and absence of anticapsular immunog
lobulin G1 (IgG1) and IgE monoclonal antibody (MAb). Eosinophils phago
cytosed C. neoformans only in the presence of specific antibody. Phago
cytosis was rapid, and dense rings that appeared to consist of granule
contents were formed around the organisms. Mast cells were observed t
o occasionally phagocytose C. neoformans in vitro in the presence of I
gE MAb. Our observations suggest that eosinophils may be effector cell
s against C. neoformans.