Kavaz Tufan Asli, Ozak Batibay Fatma, Kaya Aksoy Gulsah, Gulhan Bora, Demircioglu Kilic Beltinge, Dursun Ismail, Buyukkaragoz Bahar, Caltik Yilmaz Aysun, Nalcacioglu Hulya, Becerir Tulay, Cetin Nuran, Celegen Kubra, Dinleyici Meltem, Kaya Mucahit, Kilic Omer, Dinleyici Ener Cagri
Department of Pediatric Nephrology, Faculty of Medicine, Eskisehir Osmangazi University, 26040 Eskisehir, Türkiye.
Department of Pediatric Nephrology, Faculty of Medicine, Akdeniz University, 07070 Antalya, Türkiye.
Children (Basel). 2024 Sep 25;11(10):1164. doi: 10.3390/children11101164.
BACKGROUND/OBJECTIVES: Eculizumab is a first-line treatment for atypical hemolytic uremic syndrome (aHUS), and patients undergoing eculizumab therapy may become more susceptible to infection caused by (). While meningococcal vaccination is required for patients undergoing eculizumab therapy, there is limited knowledge about meningococcal carriage in children with aHUS. We aimed to evaluate (1) the prevalence of carriage, (2) serogroup distribution, and (3) the immunization status of children undergoing eculizumab treatment for aHUS.
The Meningo-aHUS study is a prospective, multi-center study evaluating meningococcal carriage in children and adolescents in Türkiye receiving eculizumab for aHUS. We noted the age, gender, daycare, school, or university attendance, passive smoking status, previous infection and antibiotic use, and previous immunization history, including meningococcal vaccines, from the medical records of those children with aHUS. We collected nasopharyngeal samples, tested them for using real-time polymerase chain reaction, and performed a serogroup analysis on the positive samples.
We collected nasopharyngeal samples from 62 children with aHUS. Out of 62 children, 61 (98.4%) had received at least one dose of the meningococcal vaccine. The median time since the last meningococcal vaccine dose was 15 months (1-59 months). We detected meningococcal carriage in three (4.8%, 95% CI 1.0-13.5) children, and all three strains were non-groupable (NG). No other serogroups were detected.
Almost all the children received their risk-group meningococcal immunization, including booster doses. A 4.8% of children with aHUS carried NG meningococci and, no vaccine serogroups were detected. Patients treated with eculizumab remain profoundly susceptible to IMD due to these NG meningococcal strains. The occurrence of breakthrough cases and carriage of , especially NG strains, highlights the significance of maintaining a state of constant alertness, promptly seeking medical attention, and swiftly treating any symptoms that align with IMD, regardless of their vaccination status or antibiotic prophylaxis.
背景/目的:依库珠单抗是治疗非典型溶血性尿毒症综合征(aHUS)的一线药物,接受依库珠单抗治疗的患者可能更容易感染由()引起的疾病。虽然接受依库珠单抗治疗的患者需要接种脑膜炎球菌疫苗,但对于aHUS患儿的脑膜炎球菌携带情况了解有限。我们旨在评估(1)携带情况的患病率,(2)血清群分布,以及(3)接受依库珠单抗治疗aHUS的儿童的免疫状态。
Meningo-aHUS研究是一项前瞻性、多中心研究,评估在土耳其接受依库珠单抗治疗aHUS的儿童和青少年中的脑膜炎球菌携带情况。我们从这些aHUS患儿的病历中记录年龄、性别、日托、学校或大学就读情况、被动吸烟状况、既往感染和抗生素使用情况,以及既往免疫史,包括脑膜炎球菌疫苗接种情况。我们采集鼻咽样本,使用实时聚合酶链反应对其进行检测,并对阳性样本进行血清群分析。
我们从62例aHUS患儿中采集了鼻咽样本。在62例患儿中,61例(98.4%)至少接种过一剂脑膜炎球菌疫苗。自上次接种脑膜炎球菌疫苗以来的中位时间为15个月(1 - 59个月)。我们在3例(4.8%,95%CI 1.0 - 13.5)患儿中检测到脑膜炎球菌携带,所有3株菌株均不可分组(NG)。未检测到其他血清群。
几乎所有儿童都接受了风险组脑膜炎球菌免疫接种,包括加强剂量。4.8%的aHUS患儿携带NG脑膜炎球菌,未检测到疫苗血清群。由于这些NG脑膜炎球菌菌株,接受依库珠单抗治疗的患者仍然极易感染侵袭性脑膜炎球菌病。突破性病例的出现以及(尤其是NG菌株)的携带情况,凸显了保持持续警惕状态、及时就医以及迅速治疗任何与侵袭性脑膜炎球菌病相符症状的重要性,无论其疫苗接种状况或抗生素预防情况如何。