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The International Journal of the Royal Society of Thailand
              Volume XI - 2019



              by combining the vaccine with antimalarial prophylactic drugs aiming to increase
              the duration of malaria protection.

                      Before evaluating RTS,S/AS01 in large-scale trials we assessed whether
              the vaccine, administered with and without antimalarial drugs, is safe and
              immunogenic. The study recruited 193 healthy adult volunteers randomized

              to 7 arms of variable regimens of RTS,S with and without the MDA regimen
              (dihydroartemisinin-piperaquine) plus primaquine. One month after the last
              vaccination all study participants had seroconversion of the PfCSP (NANP)6 and
              the PfCSP Full Length (N + C-Terminal). More than 90% of vaccine recipients had
              seroconverted to the Pfanti-C-Term CSP. All studied subjects were followed for
              6 months. The results showed no drug-vaccine interactions. Neither was there a
              relevant change of the drug concentrations nor the antibody levels when vaccine
              and antimalarial drugs were combined. This study found that RTS,S/AS01 with
              and without dihydroartemisinin-piperaquine plus single low dose primaquine is
              safe and immunogenic (Figure 6). This integrated approach of vaccine and
              antimalarial drugs could be useful for malaria prevention in endemic areas.

















              Figure 6 Antibodies levels of the two RTS,S doses (dash lines) and the corresponding comparison
              with RTS,S + DHA-PPQ + primaquine (solid lines). RTS,S vaccine (at monthly interval for 3
              months) is given 3 standard doses (yellow) and 2 standard doses plus 1 fractional dose (green)
              (von Seidlein et al., 2019).


                      Mass Drug Administration

                      We started a Mass Drug Administration (MDA) project in Savannakhet
              Province, Laos in 2018. The main objective was to access the effectiveness and
              safety of MDA, including the impact on asymptomatic P. falciparum infections in
              4 malaria-endemic villages (Figure 7). The population studied consisted of 1,909
              villagers. Two villages each were randomized to MDA (3 rounds of a 3-day course





              20                                   Precision Tools for Malaria Control and Mahidol University’s
                                                                    Research on the Malaria Elimination



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