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. 2004 Sep;113(1):106–113. doi: 10.1111/j.1365-2567.2004.01930.x

Table 1.

ISS-ODN modulation of Th2-biased adaptive immune profiles

Intervention %IgE increase %IgG1 increase IL-4 (pg/ml) IL-5 (pg/ml) IL-13 (pg/ml) IFN-γ (pg/ml)
None 478 ± 83 432 ± 119 2379 ± 840 2468 ± 783 146 140 ± 32 680 159 ± 23
ISS-ODN (i.d.) 187 ± 34* 166 ± 44* 472 ± 221* 154 ± 60* n.d.* 772 ± 163*
C-ODN (i.d.) 549 ± 186 798 ± 27 6086 ± 3039 2452 ± 1170 112 112 ± 21 493 173 ± 71
ISS-ODN (i.n.) 197 ± 47* 134 ± 67* 459 ± 137* 186 ± 35* 856 ± 856* 617 ± 131*
C-ODN (i.n.) 425 ± 101 413 ± 57 2517 ± 704 2459 ± 619 105 151 ± 5704 133 ± 37
DXM 200 ± 37* 286 ± 175 2782 ± 1196 902 ± 86 197 433 ± 81 995 164 ± 41

Mice (four mice/group) were sensitized and challenged as outlined in Fig. 1. Sera were collected for OVA-specific IgE and IgG1 determinations 1 day before the first and 1 day after the last i.n. OVA challenges. (Post-challenge immunoglobulin/pre-challenge immunoglobulin) × 100=% immunoglobulin increase. Splenocytes were harvested to assess OVA specific cytokine production at the time of the second bleed. Results are reflective of three separate experiments.

n.d.=none detected.

*

P ≤ 0.05 for comparisons to OVA sensitized and challenged mice receiving no intervention.