Table 1 Correlation between infliximab (IFX), anti-IFX antibodies (antibodies towards IFX, ATI) determined by SPR and ELISA in the serum of patients treated with IFX (trough levels, just before the next infusion) and clinical characteristics of the patient population during the study period.
PT ID | Centre | Diagnosis | Months of IFX therapy | Dose regimen at sampling | Disease activity | Concomitant thiopurines | IFX (μg/mL undiluted serum) | ATI (μg Eq/mL undiluted serum)§ | ||
---|---|---|---|---|---|---|---|---|---|---|
SPR | ELISA | SPR | ELISA | |||||||
#1 | ICH | CD | 29 | 2 = 5 mg/kg E4W | Remission | No | 4.76 ± 0.03 | 3.89–4.55 | <LLOQ | <LLOQ |
#2 | ICH | CD | 21 | 5 mg/kg E8W | Moderate | No | 7.70 ± 0.13 | 6.92–7.86 | <LLOQ | <LLOQ |
#3 | ICH | CD | 29 | 5 mg/kg E8W | Remission | No | 3.03 ± 0.03 | 3.57–3.22 | <LLOQ | <LLOQ |
#4 | ICH | UC | 97 | 5 mg/kg E8W | Remission | No | 2.31 ± 0.01 | 2.57–2.74 | <LLOQ | <LLOQ |
#5 | ICH | CD | 46 | 5 mg/kg E8W | Remission | No | 2.63 ± 0.02 | 2.76-2.77 | <LLOQ | <LLOQ |
#6 | ICH | CD | 30 | 5 mg/kg E8W | Mild | No | <LLOQ | <LLOQ | 37.57 ± 0.21 | 3.9-4.0* |
#7 | ICH | CD | 22 | 5 mg/kg E8W | Remission | No | <LLOQ | <LLOQ | <LLOQ | 0.04–0.07 |
#8 | ICH | UC | 7 | 5 mg/kg E8W | Remission | Yes | <LLOQ | <LLOQ | 6.64 ± 0.14 | over |
#9 | ICH | CD | 30 | 5 mg/kg E8W | Remission | No | 7.48 ± 0.02 | 6.61–7.90 | <LLOQ | <LLOQ |
#10 | ICH | UC | 3 | 5 mg/kg E8W | Remission | No | <LLOQ | <LLOQ | 5.67 ± 0.10 | 0.57–0.63* |
#11 | ICH | CD | 7 | 5 mg/kg E8W | Remission | No | 1.39 ± 0.05 | 1.52–1.69 | 2.54 ± 0.04 | <LLOQ |
#12 | FI | CD | 4 | 5 mg/kg E8W | Mild | Yes | 4.62 ± 0.10 | 4.84–5.32 | <LLOQ | <LLOQ |
#13 | FI | CD | 4 | 5 mg/kg E8W | Remission | No | 4.09 ± 0.03 | 4.13–4.32 | <LLOQ | <LLOQ |
#14 | FI | CD | 5 | 5 mg/kg E8W | Remission | No | 4.11 ± 0.04 | 3.98–4.35 | <LLOQ | <LLOQ |
#15 | FI | UC | 7 | 5 mg/kg E8W | Remission | No | <LLOQ | <LLOQ | 3.60 ± 0.34 | 0.08-0.09 |