In contrast to HBV-specific IFN-γ+ responses that did not differ significantly between phases (Figure 1 B), HBV-specific (background subtracted) IL-2+ SFU were significantly higher in IC compared to IA+ patients ( p =0.0185) and approached significance between IC and IT patients (Figure 1 E).
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IL-2 produced by HBV-specific T cells as a biomarker of viral control and predictor of response to PD-1 therapy across clinical phases of chronic hepatitis B.
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