With a murine model of invasive aspergillosis we investigated cytokine production by CD4(+) T helper cells and the effects of cytokine administration or neutralization on the course and outcome of infection. Patterns of susceptibility and resistance to infection were obtained with different strains of mice injected with different inocula of Aspergillus fumigatus conidia. Mice surviving the primary infection also resisted a subsequent lethal infection that was associated with production of gamma interferon by CD4(+) T splenocytes. Impaired neutrophil antifungal activity, observed in susceptible mice, was concomitant with a predominant production of interleukin-4 (IL-4) by CD4(+) splenocytes. In these mice, exogenous administration of IL-12 failed to induce resistance to infection; in contrast, treatment with soluble IL-4 receptor cured more than 70% of the mice from primary infection and resulted in the onset of acquired resistance to a subsequent lethal infection. These findings indicate that in murine invasive aspergillosis, production of IL-4 by CD4(+) T cells may be one major factor discriminating susceptibility and resistance to infection.
机构:
HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
NICKERSON, P
STEURER, W
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HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
STEURER, W
STEIGER, J
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HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
STEIGER, J
ZHENG, XX
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HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
ZHENG, XX
STEELE, AW
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HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
STEELE, AW
STROM, TB
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HARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USAHARVARD UNIV, BETH ISRAEL HOSP, SCH MED, DIV IMMUNOL, BOSTON, MA 02215 USA
机构:
Univ New Mexico, Sch Med, Albuquerque Vet Affairs Med Ctr, Albuquerque, NM 87108 USAUniv New Mexico, Sch Med, Albuquerque Vet Affairs Med Ctr, Albuquerque, NM 87108 USA
Schuyler, M
JOURNAL OF LABORATORY AND CLINICAL MEDICINE,
1998,
131
(03):
: 194
-
196
机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USA
Rose, S
Abdulghani, A
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USA
Abdulghani, A
Raja, K
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USA
Raja, K
Chandramouli, R
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USA
Chandramouli, R
Gottlieb, A
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USAUniv Med & Dent New Jersey, Robert Wood Johnson Med Sch, Clin Res Ctr, Div Clin Pharmacol, New Brunswick, NJ 08903 USA