期刊
CURRENT OPINION IN INFECTIOUS DISEASES
卷 16, 期 6, 页码 553-558出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00001432-200312000-00007
关键词
Plasmodium falciparum; genetic markers for drug resistance; chloroquine; antifolates; mefloquine
Purpose of review Malaria and the increasing role of drug resistance as an obstacle to its control are global problems. The identification and implications of molecular markers for antimalarial drug resistance - the subject of this review - are key issues in elucidating and eventually controlling resistance. Recent findings Recent achievements include the successful expression of the Plasmodium falciparum chloroquine resistance transporter gene, pfcrt, in yeast, the identification of polymorphisms on the gamma-glutamylcysteine synthetase gene, ggcs, as potential determinants of chloroquine and mefloquine resistance, and the usefulness of a combined Plasmodium falciparum dihydrofolate reductase gene, pfdhfr, 59(ARG) and Plasmodium falciparum dihydropteroate synthase gene, pfdhps, 540(GLU) marker in reliably representing resistance to antifolates. Moreover, treatment with sulfadoxine-pyrimethamine in the presence of pfdhfr 108(ASP) alone delayed parasite clearance and increased gametocytogony without an overt loss of the overall therapeutic efficacy of the drug. Summary The use of pfdhfr and pfdhps markers in determining antifolate resistance of Plasmodium falciparum has been consolidated. Similar progress has been made with pfcrt markers for chloroquine resistance, auguring well the operational deployment of molecular techniques. Regarding the molecular basis of resistance to arylaminoalcolhols, related drugs, and artemisinin and its derivatives, answers remain elusive, but there are promising new leads.
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