Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland, USA.
mBio. 2024 Aug 14;15(8):e0107924. doi: 10.1128/mbio.01079-24. Epub 2024 Jul 12.
Surveillance and sustained control of visceral leishmaniasis (VL) require reliable serodiagnostic tools. rK39, the gold standard antigen for VL diagnosis, is limited by its documented poor sensitivity in certain endemic regions, such as East Africa, and by the longevity of its antibodies, making it difficult to distinguish active from cured infections. In a recent publication in , Roberts et al. (A. J. Roberts, H.B. Ong, S. Clare, C. Brandt, et al., mBio 15:e00859-24, 2024, https://doi.org/10.1128/mbio.00859-24) identified new immunogenic candidates in dogs and humans. In dogs, combined antigens LdBPK_290790.1 + LdBPK_362700.1 (D4 +D46) distinguished symptomatic from asymptomatic infections. For humans, LdBPK_323600.1 (D36) antigen produced short-lived antibodies and performed well in patient cohorts from Bangladesh and Ethiopia, but not Kenya. This study adds promising new candidates to our serodiagnostic toolbox but highlights the need for more antigen discovery studies that may have to be focused on regional performance.
监测和持续控制内脏利什曼病(VL)需要可靠的血清诊断工具。rK39 是 VL 诊断的金标准抗原,但在东非等某些流行地区,其灵敏度存在问题,且抗体持续时间长,难以区分活动性感染和已治愈的感染。在最近发表于 的一篇文章中,Roberts 等人(A. J. Roberts、H.B. Ong、S. Clare、C. Brandt 等人,mBio 15:e00859-24, 2024, https://doi.org/10.1128/mbio.00859-24)在狗和人类中发现了新的免疫原性候选物。在狗中,组合抗原 LdBPK_290790.1 + LdBPK_362700.1(D4+D46)可区分有症状和无症状感染。对于人类,LdBPK_323600.1(D36)抗原产生的抗体持续时间短,在来自孟加拉国和埃塞俄比亚的患者队列中表现良好,但在肯尼亚则不然。这项研究为我们的血清诊断工具包增加了有前途的新候选物,但强调需要进行更多的抗原发现研究,这些研究可能必须侧重于区域性能。