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Infect. Immun., 07 1996, 2556-2562, Vol 64, No. 7
V McDonald, HA Robinson, JP Kelly and GJ Bancroft
The role of gut intraepithelial lymphocytes (IEL) in immunity to
cryptosporidial infection was investigated with a murine infection model
involving Cryptosporidium muris. Oocyst shedding was monitored in severe
combined immunodeficiency (SCID) mice infected with C. muris following
intravenous injection of mesenteric lymph node (MLN) cells or intestinal
IEL from BALB/c donor mice which were naive or previously infected with C.
muris. SCID mice receiving no lymphoid cells developed chronic infections
and excreted large numbers of oocysts until the end of the experiment. SCID
mice injected with IEL from immune animals, however, were able to overcome
the infection, and furthermore, these animals produced fewer oocysts and
recovered sooner than ones which received IEL or MLN cells from naive
BALB/c donors. Similar levels of protection were obtained in SCID mice
injected with either 2 X 10(6) IEL or MLN cells from immune donor mice.
Depletion of CD4+ cells from immune IEL, however, abrogated the ability to
transfer immunity to SCID mice, while depletion of CD8+ cells only
marginally reduced the protective capacity of immune IEL. Finally, control
SCID mice which received no lymphocytes had < or = 1% CD4+ cells in the
IEL from the small intestine, whereas the IEL from SCID mice recovered from
infection, as a result of injection with immune IEL, contained 15% CD4+
cells. Thus, the ability to control C. muris infection correlated with the
presence of the protective CD4+ cells in the gut epithelium.
Copyright © 1996, American Society for Microbiology
Immunity to Cryptosporidium muris infection in mice is expressed through gut CD4+ intraepithelial lymphocytes
Department of Clinical Sciences, London School of Hygiene and Tropical Medicine, London, United Kingdom.
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