Circulation, Vol 82, 982-989, Copyright © 1990 by American Heart Association
C Kishimoto, KA Thorp and WH Abelmann
To test the therapeutic efficacy of immunosuppression with cyclophosphamide
(CYP) on coxsackievirus B3 (CB3) myocarditis, 2-week- old DBA/2 mice were
inoculated with 3 X 10(2) plaque-forming units of CB3 virus. CYP (100
mg/kg/day s.c.) was administered daily on days 0-8 (experiment 1; group 2),
days 8-21 (experiment 2; group 4), and days 21- 34 (experiment 3; group 6).
Groups 1, 3, and 5 were infected control groups for each experiment.
Spleen, thymus, and body weights were measured. In experiment 1, survival
rate in group 2 on day 8 was low compared with group 1 (nine of 51 versus
eight of 28; p = NS), and myocardial virus titers in group 2 on day 8 were
higher (p less than 0.05) compared with group 1; however, cellular
infiltration and myocardial necrosis in group 2 were less severe (p less
than 0.05), and serum neutralizing antibody titers were decreased (p less
than 0.01). In experiment 2, survival rate in group 4 on day 21 was
significantly lower (six of 24 versus 12 of 16; p less than 0.01), but
cellular infiltration, myocardial necrosis, and calcification in group 4
were significantly less severe, and serum neutralizing antibody titers were
decreased (p less than 0.01). In experiment 3, survival rate, cardiac
histopathology, and serum neutralizing antibody titers did not differ
between groups 5 and 6. In experiments 1, 2, and 3, the treated groups were
characterized by lower spleen-to-body-weight and thymus-to-body- weight
ratios and by marked cellular depletion in spleen and thymus.(ABSTRACT
TRUNCATED AT 250 WORDS)
ARTICLES
Immunosuppression with high doses of cyclophosphamide reduces the severity of myocarditis but increases the mortality in murine Coxsackievirus B3 myocarditis
Charles A. Dana Research Institute, Beth Israel Hospital, Boston, MA 02215.
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