Why the study?
Does LS 2616 reduce myocardial damage and alter lymphocyte subpopulations in murine Coxsackievirus B3 myocarditis?
Does LS 2616 reduce myocardial damage and alter lymphocyte subpopulations in murine Coxsackievirus B3 myocarditis?
In a murine model of Coxsackievirus B3 myocarditis, the immunomodulator LS 2616 reduced myocardial damage and altered lymphocyte subpopulations, suggesting potential therapeutic utility.
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Hypothesis-generating for LS 2616 in murine viral myocarditis; requires human trials before clinical consideration.
Quinoline-3-carboxamide (LS 2616) is a broadly acting immunostimulator with anti-inflammatory effects in Coxsackie virus B3-induced myocarditis in female BALB/c mice. This infection caused extensive inflammatory and necrotic lesions in the myocardium 7 days after inoculation (6.8% of tissue section area). The damaged area was reduced (to 3.7% (p less than 0.05] and the lethality decreased when LS 2616 was administered over 14 days, starting 7 days before the inoculation. The response pattern of lymphocyte subsets in situ in myocardial inflammatory lesions was elucidated by a newly developed immune histochemical staining technique. LS 2616 increased the number of class II-expressing cells 3-fold (p less than 0.01) and the CTL, Ts:Th cell ratio by 55% (p less than 0.05), whereas Lyt-1+ and TIB+ cells were unaffected. After 7 days of LS 2616 treatment, spleen lymphocyte activity tended to increase (T cells by 21% (NS) and B cells by 60% (p less than 0.05), respectively). The activity of NK cells increased by 51% (p less than 0.01). LS 2616 may thus have potential in therapy of human inflammatory disorders, such as myocarditis.
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Ilbäck et al. (1989) studied this question.
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