Tweyongyere Robert, Mawa Patrice A, Emojong Nicholas O, Mpairwe Harriet, Jones Frances M, Duong Trinh, Dunne David W, Vennervald Birgitte J, Katunguka-Rwakishaya Eli, Elliott Alison M
Faculty of Veterinary Medicine, Makerere University, Kampala, Uganda.
BMC Infect Dis. 2009 Mar 18;9:32. doi: 10.1186/1471-2334-9-32.
Praziquantel treatment of schistosomiasis during pregnancy was only recommended in 2002; hence the effects of treatment during pregnancy are not fully known. We have therefore evaluated the effects on infection intensity and the immunological effects of praziquantel treatment against Schistosoma mansoni during pregnancy, compared with treatment after delivery.
A nested cohort of 387 Schistosoma mansoni infected women was recruited within a larger trial of de-worming during pregnancy. Women were randomised to receive praziquantel or placebo during pregnancy. All women were treated after delivery. Infection intensity after treatment was assessed by a single Kato-Katz examination of stool samples with duplicate slides and categorised as undetected, light (1-99 eggs per gram (epg)), moderate (100-399 epg) or heavy (>or=400 epg). Antibodies against S. mansoni worm and egg antigens were measured by ELISA. Results were compared between women first treated during pregnancy and women first treated after delivery.
At enrollment, 252 (65.1%) of the women had light infection (median (IQR) epg: 35 (11, 59)), 75 (19.3%) moderate (median (IQR) epg: 179(131, 227)) and 60 (15.5%) had heavy infection (median (IQR) epg: 749 (521, 1169)) with S. mansoni. At six weeks after praziquantel treatment during pregnancy S. mansoni infection was not detectable in 81.9% of the women and prevalence and intensity had decreased to 11.8% light, 4.7% moderate and 1.6% heavy a similar reduction when compared with those first treated after delivery (undetected (88.5%), light (10.6%), moderate (0.9%) and heavy (0%), p = 0.16). Parasite specific antibody levels were lower during pregnancy than after delivery. Praziquantel treatment during pregnancy boosted anti-worm IgG isotypes and to a lesser extent IgE, but these boosts were less pronounced than in women whose treatment was delayed until after delivery. Praziquantel had limited effects on antibodies against egg antigens.
S mansoni antigen-specific antibody levels and praziquantel-induced boosts in antibody levels were broadly suppressed during pregnancy, but this was not associated with major reduction in the efficacy of praziquantel. Long-term implications of these findings in relation to resistance to re-infection remain to be explored.
吡喹酮治疗妊娠期血吸虫病直到2002年才被推荐使用;因此,孕期治疗的效果尚不完全清楚。我们因此评估了孕期吡喹酮治疗曼氏血吸虫病对感染强度的影响以及免疫效应,并与产后治疗进行比较。
在一项更大规模的孕期驱虫试验中招募了387名感染曼氏血吸虫病的女性组成嵌套队列。这些女性被随机分为在孕期接受吡喹酮或安慰剂治疗。所有女性在产后均接受治疗。治疗后通过对粪便样本进行单份粪便的加藤厚涂片检查(一式两份玻片)评估感染强度,并分类为未检测到、轻度(每克粪便含1 - 99个虫卵(epg))、中度(100 - 399 epg)或重度(≥400 epg)。通过酶联免疫吸附测定法(ELISA)检测针对曼氏血吸虫虫体和虫卵抗原的抗体。比较孕期首次接受治疗的女性和产后首次接受治疗的女性的结果。
入组时,252名(65.1%)女性为轻度感染(中位数(四分位间距)epg:35(11,59)),75名(19.3%)为中度感染(中位数(四分位间距)epg:179(131,227)),60名(15.5%)为重度感染(中位数(四分位间距)epg:749(521,1169))。孕期接受吡喹酮治疗六周后,81.9%的女性未检测到曼氏血吸虫感染,患病率和感染强度降至轻度(11.8%)、中度(4.7%)和重度(1.6%),与产后首次接受治疗的女性相比有类似程度的降低(未检测到(88.5%)、轻度(10.6%)、中度(0.9%)和重度(0%),p = 0.16)。孕期寄生虫特异性抗体水平低于产后。孕期吡喹酮治疗可增强抗虫IgG同种型,在较小程度上增强IgE,但这些增强作用不如治疗延迟至产后的女性明显。吡喹酮对针对虫卵抗原的抗体影响有限。
孕期曼氏血吸虫抗原特异性抗体水平和吡喹酮诱导的抗体水平增强在很大程度上受到抑制,但这与吡喹酮疗效的大幅降低无关。这些发现对再次感染抵抗力的长期影响仍有待探索。