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. 2015 Dec;15(12):1450–1458. doi: 10.1016/S1473-3099(15)00239-X

Table 2.

Determinants of immunogenicity of RTS,S

Primary schedule (n=2650)
Booster dose (n=1093)
Estimate (95% CI) p value Estimate (95% CI) p value
RTS,S (5–17 months): intercept 3·01 (2·91 to 3·10) .. 1·36 (1·08 to 1·65) ..
RTS,S (6–12 weeks) −0·88 (−1·00 to −0·76) <0·0001 −0·62 (−0·07 to −0·28) <0·0001
Age (5–17 months)* −0·015 (−0·022 to −0·009) <0·0001 −0·006 (−0·015 to 0·003) 0·19
Age (6–12 weeks)* 0·022 (−0·038 to 0·081) 0·48 0·085 (−0·0002 to 0·174) 0·058
HIV positive −0·53 (−0·64 to −0·42) <0·0001 −0·22 (−0·51 to 0·07) 0·136
log10(CSbase; 5–17 months) 0·14 (0·05 to 0·24) 0·003 .. ..
log10(CSbase; 6–12 weeks) −0·58 (−0·70 to −0·46) <0·0001 .. ..
log10(CSpeak; 5–17 months) .. .. 0·42 (0·34 to 0·51) <0·0001
log10(CSpeak; 6–12 weeks) .. .. 0·17 (0·06 to 0·29) 0·0025

Estimates from linear regression analyses of the effect of covariates on peak anti-circumsporozoite antibody titre after primary vaccination of RTS,S/AS01 (log10[CSpeak/(EU/mL)]) or after a booster dose (log10[CSboost/(EU/mL)]). The intercept is taken to be vaccination of a child aged 5–17 months. Trial site was included in the regression models as a random effect. Transmission intensity, sex, preterm delivery, low weight-for-age Z score, and previous cases of clinical malaria were all tested as covariates but were not significant (appendix).

*

Change associated with a 1 month change in age.

Change associated with a ten-fold change in titre.