Nguyen-Dinh P, Schwartz I K, Sexton J D, Egumb B, Bolange B, Ruti K, Nkuku-Pela N, Wery M
Bull World Health Organ. 1985;63(2):325-30.
From April to June 1983, combined in vivo and in vitro studies were conducted to assess the response to chloroquine of Plasmodium falciparum in Kinshasa and Mbuji-Mayi, Zaire. A total of 109 patients were treated with chloroquine, either as a single dose of 10 mg/kg or as a full dose of 25 mg/kg. All patients rapidly cleared their asexual parasitaemia, no recurrence being noted during the subsequent 3 weeks of follow-up. In the fourth week, recurrences were noted in 3 out of 66 patients treated with the full dose of chloroquine and in 10 out of 43 patients treated with the single dose. A total of 101 in vitro tests (30 macro tests, 39 micro tests, and 32 48-hour tests) were successfully performed with blood samples collected from 51 of these patients. Full sensitivity to chloroquine was demonstrated in all but 3 of the successful in vitro tests, the results from these 3 tests being contradicted either by alternative in vitro tests or by the corresponding in vivo findings. These investigations thus failed to detect chloroquine resistance at the level reported in East Africa or eastern Zaire (in Kivu).
1983年4月至6月,在扎伊尔的金沙萨和姆布吉-马伊开展了体内和体外联合研究,以评估恶性疟原虫对氯喹的反应。共有109名患者接受了氯喹治疗,剂量为10毫克/千克单剂量或25毫克/千克全剂量。所有患者均迅速清除了无性疟原虫血症,在随后3周的随访中未发现复发情况。在第四周,接受全剂量氯喹治疗的66名患者中有3名复发,接受单剂量治疗的43名患者中有10名复发。从其中51名患者采集的血样成功进行了总计101次体外试验(30次宏观试验、39次微观试验和32次48小时试验)。除3次成功的体外试验外,其余试验均显示对氯喹完全敏感,这3次试验的结果与其他体外试验结果或相应的体内研究结果相矛盾。因此,这些研究未能检测到东非或扎伊尔东部(基伍)报告水平的氯喹耐药性。