Sadiq Asma, Khan Jadoon
Department of Microbiology, University of Jhang, Jhang, Pakistan.
Department of Allied and Health Sciences, IQRA University, Chak Shahzad Campus, Islamabad, Pakistan.
Front Microbiol. 2024 Jan 5;14:1297269. doi: 10.3389/fmicb.2023.1297269. eCollection 2023.
Rotavirus (RV) causes the loss of numerous children's lives worldwide each year, and this burden is particularly heavy in low- and lower-middle-income countries where access to healthcare is limited. RV epidemiology exhibits a diverse range of genotypes, which can vary in prevalence and impact across different regions. The human genotypes that are most commonly recognized are G1P[8], G2P[4], G3P[8], G4P[8], G8P[8], G9P[8], and G12P[8]. The diversity of rotavirus genotypes presents a challenge in understanding its global distribution and developing effective vaccines. Oral, live-attenuated rotavirus vaccines have undergone evaluation in various contexts, encompassing both low-income and high-income populations, demonstrating their safety and effectiveness. Rotavirus vaccines have been introduced and implemented in over 120 countries, offering an opportunity to assess their effectiveness in diverse settings. However, these vaccines were less effective in areas with more rotavirus-related deaths and lower economic status compared to wealthier regions with fewer rotavirus-related deaths. Despite their lower efficacy, rotavirus vaccines significantly decrease the occurrence of diarrheal diseases and related mortality. They also prove to be cost-effective in regions with a high burden of such diseases. Regularly evaluating the impact, influence, and cost-effectiveness of rotavirus vaccines, especially the newly approved ones for worldwide use, is essential for deciding if these vaccines should be introduced in countries. This is especially important in places with limited resources to determine if a switch to a different vaccine is necessary. Future research in rotavirus epidemiology should focus on a comprehensive understanding of genotype diversity and its implications for vaccine effectiveness. It is crucial to monitor shifts in genotype prevalence and their association with disease severity, especially in high-risk populations. Policymakers should invest in robust surveillance systems to monitor rotavirus genotypes. This data can guide vaccine development and public health interventions. International collaboration and data sharing are vital to understand genotype diversity on a global scale and facilitate the development of more effective vaccines.
轮状病毒(RV)每年在全球导致众多儿童死亡,在医疗保健服务有限的低收入和中低收入国家,这一负担尤为沉重。RV流行病学呈现出多种基因型,其流行率和影响在不同地区可能有所不同。最常见的人类基因型是G1P[8]、G2P[4]、G3P[8]、G4P[8]、G8P[8]、G9P[8]和G12P[8]。轮状病毒基因型的多样性给了解其全球分布和开发有效疫苗带来了挑战。口服减毒活轮状病毒疫苗已在各种环境中进行了评估,包括低收入和高收入人群,证明了其安全性和有效性。轮状病毒疫苗已在120多个国家引入和实施,为评估其在不同环境中的有效性提供了机会。然而,与轮状病毒相关死亡较少的富裕地区相比,这些疫苗在轮状病毒相关死亡较多且经济地位较低的地区效果较差。尽管效力较低,但轮状病毒疫苗显著降低了腹泻疾病的发生率和相关死亡率。它们在这类疾病负担较高的地区也被证明具有成本效益。定期评估轮状病毒疫苗,特别是新批准的全球使用疫苗的影响、作用和成本效益,对于决定这些疫苗是否应在各国引入至关重要。在资源有限的地方,这对于确定是否需要改用不同疫苗尤为重要。未来轮状病毒流行病学的研究应侧重于全面了解基因型多样性及其对疫苗有效性的影响。监测基因型流行率的变化及其与疾病严重程度的关联至关重要,尤其是在高危人群中。政策制定者应投资建立强大的监测系统来监测轮状病毒基因型。这些数据可指导疫苗开发和公共卫生干预措施。国际合作和数据共享对于在全球范围内了解基因型多样性和促进开发更有效的疫苗至关重要。