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Infect. Immun., 05 1995, 1645-1651, Vol 63, No. 5
SM Muth and JW Murphy
Immunizing CBA/J mice with intact Cryptococcus neoformans cells or with a
cryptococcal culture filtrate antigen (CneF) induces an anticryptococcal
delayed-type hypersensitivity response. Recently, it has been shown that
two phenotypically different T-cell populations are responsible for
delayed-type hypersensitivity reactivity in mice immunized with intact
cryptococcal cells, whereas only one of those populations is present in
mice immunized with soluble cryptococcal antigens in complete Freund's
adjuvant (CFA). The purpose of this study was to determine if differences
occur with regard to direct anticryptococcal activity between
T-lymphocyte-enriched populations from mice immunized with intact viable or
dead cryptococcal cells and similar cell populations from mice immunized
with the soluble cryptococcal culture filtrate antigen, CneF, emulsified in
CFA. The percentage of lymphocytes which form conjugates with C. neoformans
and the percentage of cryptococcal growth inhibition in vitro are greater
with T-lymphocyte-enriched populations from mice sublethally infected with
C. neoformans or from mice immunized with intact heat-killed cryptococcal
cells in the presence or absence of CFA than with lymphocyte populations
from mice immunized with CneF-CFA. Enhanced anticryptococcal activity of T
lymphocytes could be induced by immunizing mice with heat-killed C.
neoformans cells of serotype A, B, C, or D as well as by immunizing with a
similar preparation of an acapsular C. neoformans mutant but not by
immunizing with CFA emulsified with CneF prepared from any one of the C.
neoformans isolates. These data indicate that the soluble cryptococcal
culture filtrate antigens do not induce the same array of functional T
lymphocytes as whole cryptococcal cells.
Copyright © 1995, American Society for Microbiology
Effects of immunization with Cryptococcus neoformans cells or cryptococcal culture filtrate antigen on direct anticryptococcal activities of murine T lymphocytes
Department of Microbiology and Immunology, University of Oklahoma Health Science Center, Oklahoma City 73190, USA.
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