TABLE 3.
Treatment groupb | Body wt (g) on day 0c | % Body wt gain at day 56c | Survival
|
Liver wt and burdensd
|
Other target organsd
|
|||||
---|---|---|---|---|---|---|---|---|---|---|
No. of survivors at necropsy | Day post- infectionc | Wt (mg)c | LDUc | % Reduc- tion | Spleen wt (mg)c | No. of animals with positive:
|
||||
Spleen | Bone marrow | |||||||||
Treatment of acute infection on day 1 postinfection | ||||||||||
Control (no treatment) | 188 ± 38 | −69 ± 6 | 2 | 53 ± 5 | 8,056 ± 1,382 | 100,147 ± 58,715 | 828 ± 66 | 2 | 2 | |
MB-III at 0.2 mg/kg s.c. | 161 ± 16 | −52 ± 17 | 2 | 54 ± 3 | 7,082 ± 2,642 | 17,012 ± 21,508 | 83.0 | 1,477 ± 1,160 | 2 | 2 |
MB-III at 0.4 mg/kg s.c. | 200 ± 12 | −8 ± 7 | 3 | 51 ± 7 | 10,614 ± 2,663 | 172 ± 297 | 99.8 | 2,007 ± 1,563 | 3 | 3 |
MB-III at 0.8 mg/kg s.c. | 176 ± 30 | 6 ± 9 | 4 | 54 ± 5 | 9,608 ± 2543 | 0 ± 0 | 100 | 666 ± 195 | 4 | 0 |
Amphotericin Be at 5 mg/kg i.v.f | 163 ± 29 | 17 ± 8 | 5 | 56 ± 0 | 9,317 ± 1302 | 0 ± 0 | 100 | 629 ± 456 | 4 | 2 |
Treatment of chronic infection on day 28 postinfection | ||||||||||
Control (no treatment) | 142 ± 18 | NAg | 0 | 50 ± 7 | NDh | ND | ND | ND | ND | |
MB-III at 0.2 mg/kg s.c. | 157 ± 30 | NA | 0 | 48 ± 12 | ND | ND | ND | ND | ND | ND |
MB-III at 0.4 mg/kg s.c. | 146 ± 23 | NA | 0 | 68 ± 14 | ND | ND | ND | ND | ND | ND |
MB-III at 0.8 mg/kg s.c. | 158 ± 39 | −36 ± 13 | 3 | 78 ± 9 | 10,067 ± 1,972 | 5 ± 6 | ND | 475 ± 181 | 0 | 0 |
Amphotericin B at 5 mg/kg i.v.f | 173 ± 35 | −38 ± 26 | 3 | 81 ± 4 | 34,901 ± 39,093 | 1,347 ± 2,298 | ND | 572 ± 224 | 0 | 0 |
Early effects of treatment were determined by necropsy at day 56 posttreatment.
Groups of five animals each (males and females) received a single dose.
Values are means ± standard deviations.
Only survivers were evaluated.
Liposomal amphotericin B (AmBisome).
i.v., intravenously.
NA, not applicable.
ND, not done.