Table 3.
Donor of DCs | Recipient with EAM after challenge | Mean score (0+–4+) ± SD |
---|---|---|
S2-16:IFA | 1/8 | 0 ± 0.3* |
S2-16:IFA (+ anti-IL-10) | 4/6 | 1.9 ± 1.8 |
S2-1:IFA | 0/3 | 0† |
PBS:IFA | 0/3 | 0† |
S2-16:CFA | 6/8 | 1.6 ± 1.1 |
Naive | 4/5 | 1.7 ± 1.1 |
Lewis rats were treated with S2-16:IFA. Control rats were treated with S2-16:CFA, S2-1:IFA, PBS:IFA, or left untreated. Splenic DCs were obtained from each group of animals 2 weeks after treatment, and were cultured in vitro with peptide S2-16, together with LPS plus anti-rat CD40 antibody for 12 hours. One group of S2-16:IFA-treated rats were incubated with antibody against rat IL-10 in addition. DC aliquot (106) was injected into each naïve Lewis rat intravenously. The recipients were concomitantly challenged by active immunization with S2-16:CFA after transfer, and sacrificed 3 weeks after challenge. Myocarditis was identified in the fixed heart sections by histopathological examination.
P < 0.01 for groups: S2-16:IFA versus naïve, S2-16:IFA versus S2-16:IFA (+ anti-IL-10), and S2-16:IFA versus S2-16:CFA.
P < 0.05 for groups: S2-1:IFA versus naïve, and PBS:IFA versus naive.