Molecular epidemiology and clinical features of hand, foot and mouth disease requiring hospitalization after the use of enterovirus A71 inactivated vaccine in chengdu, China, 2017-2022: a descriptive study

Emerg Microbes Infect. 2022 Dec;11(1):2510-2519. doi: 10.1080/22221751.2022.2125346.

Abstract

Three inactivated enterovirus A71 (EV-A71) vaccines have been widely vaccinated among children in the targeted age group in mainland China since mid-2016. However, comprehensive virological surveillance of hand, foot and mouth disease (HFMD) over multiple years after the use of EV-A71 vaccines has rarely been conducted. Using long-term data extracted from the Public Health and Clinical Center of Chengdu, we described the clinical, aetiological, and epidemiological characteristics of HFMD inpatients after the use of EV-A71 vaccines from 2017 through 2022. A total of 5115 patients were selected for analysis with a male-to-female ratio of 1.63:1 and were mostly under 5 years of age (97.6%). Among these cases, 4.3% presented with severe symptoms, and 4.1% of severe cases experienced significant complications. EV-A71 was no longer the major serotype for laboratory-confirmed HFMD, responsible for 15.6% of severe cases and 1.2% of mild cases. A significant downwards trend of EV-A71 infections was observed after the use of EV-A71 vaccines (P for trend < 0.001). Coxsackievirus A6 was the predominant pathogen, accounting for 63.5% of mild cases and 36.2% of severe cases. Coxsackievirus A10 (CV-A10) and A16 were sporadically detected, and an upwards trend was observed in the proportion of CV-A10 infections. This study provides baseline molecular epidemiology for the evaluation of EV-A71 vaccination impact and potential serotype replacement based on HFMD inpatients. Additional nationwide and population-based epidemiologic and serologic studies are essential to elucidate HFMD dynamics after the use of EV-A71 vaccines, and to inform public health authorities to introduce optimized intervention strategies.

Keywords: EV-A71 vaccine; Hand foot and mouth disease; clinical features; enterovirus; molecular epidemiology.

MeSH terms

  • AIDS Vaccines*
  • Antigens, Viral
  • BCG Vaccine
  • Child
  • China / epidemiology
  • Diphtheria-Tetanus-Pertussis Vaccine
  • Enterovirus A, Human* / genetics
  • Enterovirus Infections* / diagnosis
  • Enterovirus Infections* / epidemiology
  • Enterovirus Infections* / prevention & control
  • Enterovirus* / genetics
  • Female
  • Hand, Foot and Mouth Disease* / complications
  • Hand, Foot and Mouth Disease* / epidemiology
  • Hand, Foot and Mouth Disease* / prevention & control
  • Hospitalization
  • Humans
  • Influenza Vaccines*
  • Male
  • Measles-Mumps-Rubella Vaccine
  • Molecular Epidemiology
  • Papillomavirus Vaccines*
  • Respiratory Syncytial Virus Vaccines*
  • SAIDS Vaccines*
  • Vaccines, Inactivated

Substances

  • Diphtheria-Tetanus-Pertussis Vaccine
  • antineoplaston A10
  • AIDS Vaccines
  • BCG Vaccine
  • Influenza Vaccines
  • Measles-Mumps-Rubella Vaccine
  • Respiratory Syncytial Virus Vaccines
  • SAIDS Vaccines
  • Vaccines, Inactivated
  • Antigens, Viral
  • Papillomavirus Vaccines

Grants and funding

This work was supported by the National Natural Science Foundation of China under Grant 81903375; China Postdoctoral Science Foundation under Grant 2018M643509; and Chengdu Science and Technology Bureau under Grant 2019-YF05-01080-SN.