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Infect. Immun., 01 1995, 280-288, Vol 63, No. 1
G Arancia, A Molinari, P Crateri, A Stringaro, C Ramoni, ML Dupuis, MJ Gomez, A Torosantucci and A Cassone
During incubation in vitro with yeast or germ tube forms of Candida
albicans, only 2 to 6% of freshly isolated human natural killer (NK) cells
(> 85% CD16+, CD56+, CD3-; < 15% CD3+; cytolytic for the NK-
susceptible target K562 but not for the NK-resistant target DAUDI), were
seen to interact with the fungal cells. As seen under the electron
microscope, the contact area had a limited extent and was narrow, and
neither the surface nor the intracytoplasmic organization of the NK cell
was altered. In contrast, more than 30% of interleukin-2-activated NK (LAK)
cells (> 96% CD16+, CD56+, CD3-; 1.5% CD3+; cytolytic for both K562 and
DAUDI targets) interacted closely with the fungus. This interaction was
particularly extensive with the surface of the fungal germ tube that was
intimately enveloped by villous protrusions from the lymphocyte surface.
The fungus-interacting LAK cell also showed a remarkable redistribution of
surface microvilli and polarization of cytoplasmic organelles, such as the
Golgi apparatus, centrioles, and granules, toward the area of fungal
contact. Together with the elevated cytolytic potential against the K562
and DAUDI targets, all the morphological data suggested the presence of a
potentially active lytic machinery in the fungus-interacting LAK cell.
Nonetheless, two independent assays for anticandidal activity did not show
consistent killing or fungal growth inhibition by either fresh NK or LAK
cells. While offering direct evidence of the strong interaction between
human LAK cells and the germ tubes, precursors of tissue-invasive hyphal
forms of C. albicans, our observations also suggest that this interaction
may not be sufficient to kill the fungus or arrest its growth.
Copyright © 1995, American Society for Microbiology
Noninhibitory binding of human interleukin-2-activated natural killer cells to the germ tube forms of Candida albicans
Department of Ultrastructures, Istituto Superiore di Sanita, Rome, Italy.
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