4.6 Article

Cases of Acute Flaccid Paralysis Associated with Coxsackievirus A2: Findings of a 20-Year Surveillance in the Russian Federation

期刊

MICROORGANISMS
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/microorganisms10010112

关键词

acute flaccid paralysis (AFP); coxsackievirus A2 (CV-A2); poliomyelitis; polioviruses; non-polio enteroviruses; epidemiological surveillance

资金

  1. Federal Budget of the Russian Federation
  2. WHO Polio Eradication Programme
  3. WHO Regional Office for Europe
  4. Russian Scientific Foundation (RSF) [19-15-00055]
  5. Russian Science Foundation [19-15-00055] Funding Source: Russian Science Foundation

向作者/读者索取更多资源

Surveillance for acute flaccid paralysis syndrome (AFP) in children under 15 is crucial for the Global Polio Eradication Initiative. The identification of non-polio enteroviruses (NPEV) alongside polioviruses in stool samples of AFP cases has provided valuable insights. Enteroviruses A71 and D68 have been definitively linked to AFP, while the association of Enterovirus Coxsackie A2 (CVA2) with AFP is less understood. This study suggests that CVA2 may be a cause of AFP, highlighting the importance of AFP surveillance for both polio control and the study of uncommon AFP agents.
Surveillance for acute flaccid paralysis syndrome (AFP) in children under 15 is the backbone of the Global Polio Eradication Initiative. Laboratory examination of stool samples from AFP cases allows the detection of, along with polioviruses, a variety of non-polio enteroviruses (NPEV). The etiological significance of these viruses in the occurrence of AFP cases has been definitively established only for enteroviruses A71 and D68. Enterovirus Coxsackie A2 (CVA2) is most often associated with vesicular pharyngitis and hand, foot and mouth disease. Among 7280 AFP cases registered in Russia over 20 years (2001-2020), CVA2 was isolated only from five cases. However, these included three children aged 3 to 4 years, without overt immune deficiency, immunized with 4-5 doses of poliovirus vaccine in accordance with the National Vaccination Schedule. The disease resulted in persistent residual paralysis. Clinical and laboratory data corresponded to poliomyelitis developing during poliovirus infection. These findings are compatible with CVA2 being the cause of AFP. Molecular analysis of CVA2 from these patients and a number of AFP cases in other countries did not reveal association with a specific phylogenetic group, suggesting that virus genetics is unlikely to explain the pathogenic profile. The overall results highlight the value of AFP surveillance not just for polio control but for studies of uncommon AFP agents.

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