Pediatric Respiratory and Enteric Virus Acquisition and Immunogenesis in US Mothers and Children Aged 0-2: PREVAIL Cohort Study.

RSV birth cohort immunology influenza norovirus pediatrics rotavirus vaccine effectiveness vaccines

Journal

JMIR research protocols
ISSN: 1929-0748
Titre abrégé: JMIR Res Protoc
Pays: Canada
ID NLM: 101599504

Informations de publication

Date de publication:
12 Feb 2021
Historique:
received: 14 07 2020
accepted: 12 12 2020
revised: 19 11 2020
entrez: 12 2 2021
pubmed: 13 2 2021
medline: 13 2 2021
Statut: epublish

Résumé

Acute gastroenteritis (AGE) and acute respiratory infections (ARIs) cause significant pediatric morbidity and mortality. Developing childhood vaccines against major enteric and respiratory pathogens should be guided by the natural history of infection and acquired immunity. The United States currently lacks contemporary birth cohort data to guide vaccine development. The PREVAIL (Pediatric Respiratory and Enteric Virus Acquisition and Immunogenesis Longitudinal) Cohort study was undertaken to define the natural history of infection and immune response to major pathogens causing AGE and ARI in US children. Mothers in Cincinnati, Ohio, were enrolled in their third trimester of pregnancy, with intensive child follow-up to 2 years. Blood samples were obtained from children at birth (cord), 6 weeks, and 6, 12, 18, and 24 months. Whole stool specimens and midturbinate nasal swabs were collected weekly and tested by multipathogen molecular assays. Saliva, meconium, maternal blood, and milk samples were also collected. AGE (≥3 loose or watery stools or ≥1 vomiting episode within 24 hours) and ARI (cough or fever) cases were documented by weekly cell phone surveys to mothers via automated SMS text messaging and review of medical records. Immunization records were obtained from registries and providers. follow-up ended in October 2020. Pathogen-specific infections are defined by a PCR-positive sample or rise in serum antibody. Of the 245 enrolled mother-child pairs, 51.8% (n=127) were White, 43.3% (n=106) Black, 55.9% (n=137) publicly insured, and 86.5% (n=212) initiated breastfeeding. Blood collection was 100.0% for mothers (n=245) and 85.7% for umbilical cord (n=210). A total of 194/245 (79.2%) mother-child pairs were compliant based on participation in at least 70% (≥71/102 study weeks) of child-weeks and providing 70% or more of weekly samples during that time, or blood samples at 18 or 24 months. Compliant participants (n=194) had 71.0% median nasal swab collection (IQR 30.0%-90.5%), with 98.5% (191/194) providing either an 18- or 24-month blood sample; median response to weekly SMS text message surveys was 95.1% (IQR 76.5%-100%). Compliant mothers reported 2.0 AGE and 4.5 ARI cases per child-year, of which 25.5% (160/627) and 38.06% (486/1277) of cases, respectively, were medically attended; 0.5% of AGE (3/627) and 0.55% of ARI (7/1277) cases were hospitalized. The PREVAIL Cohort demonstrates intensive follow-up to document the natural history of enteric and respiratory infections and immunity in children 0-2 years of age in the United States and will contribute unique data to guide vaccine recommendations. Testing for pathogens and antibodies is ongoing. RR1-10.2196/22222.

Sections du résumé

BACKGROUND BACKGROUND
Acute gastroenteritis (AGE) and acute respiratory infections (ARIs) cause significant pediatric morbidity and mortality. Developing childhood vaccines against major enteric and respiratory pathogens should be guided by the natural history of infection and acquired immunity. The United States currently lacks contemporary birth cohort data to guide vaccine development.
OBJECTIVE OBJECTIVE
The PREVAIL (Pediatric Respiratory and Enteric Virus Acquisition and Immunogenesis Longitudinal) Cohort study was undertaken to define the natural history of infection and immune response to major pathogens causing AGE and ARI in US children.
METHODS METHODS
Mothers in Cincinnati, Ohio, were enrolled in their third trimester of pregnancy, with intensive child follow-up to 2 years. Blood samples were obtained from children at birth (cord), 6 weeks, and 6, 12, 18, and 24 months. Whole stool specimens and midturbinate nasal swabs were collected weekly and tested by multipathogen molecular assays. Saliva, meconium, maternal blood, and milk samples were also collected. AGE (≥3 loose or watery stools or ≥1 vomiting episode within 24 hours) and ARI (cough or fever) cases were documented by weekly cell phone surveys to mothers via automated SMS text messaging and review of medical records. Immunization records were obtained from registries and providers. follow-up ended in October 2020. Pathogen-specific infections are defined by a PCR-positive sample or rise in serum antibody.
RESULTS RESULTS
Of the 245 enrolled mother-child pairs, 51.8% (n=127) were White, 43.3% (n=106) Black, 55.9% (n=137) publicly insured, and 86.5% (n=212) initiated breastfeeding. Blood collection was 100.0% for mothers (n=245) and 85.7% for umbilical cord (n=210). A total of 194/245 (79.2%) mother-child pairs were compliant based on participation in at least 70% (≥71/102 study weeks) of child-weeks and providing 70% or more of weekly samples during that time, or blood samples at 18 or 24 months. Compliant participants (n=194) had 71.0% median nasal swab collection (IQR 30.0%-90.5%), with 98.5% (191/194) providing either an 18- or 24-month blood sample; median response to weekly SMS text message surveys was 95.1% (IQR 76.5%-100%). Compliant mothers reported 2.0 AGE and 4.5 ARI cases per child-year, of which 25.5% (160/627) and 38.06% (486/1277) of cases, respectively, were medically attended; 0.5% of AGE (3/627) and 0.55% of ARI (7/1277) cases were hospitalized.
CONCLUSIONS CONCLUSIONS
The PREVAIL Cohort demonstrates intensive follow-up to document the natural history of enteric and respiratory infections and immunity in children 0-2 years of age in the United States and will contribute unique data to guide vaccine recommendations. Testing for pathogens and antibodies is ongoing.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID) UNASSIGNED
RR1-10.2196/22222.

Identifiants

pubmed: 33576746
pii: v10i2e22222
doi: 10.2196/22222
pmc: PMC7910118
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e22222

Informations de copyright

©Ardythe L Morrow, Mary A Staat, Emily A DeFranco, Monica M McNeal, Allison R Cline, Shannon C Conrey, Elizabeth P Schlaudecker, Alexandra M Piasecki, Rachel M Burke, Liang Niu, Aron J Hall, Michael D Bowen, Susan I Gerber, Gayle E Langley, Natalie J Thornburg, Angela P Campbell, Jan Vinjé, Umesh D Parashar, Daniel C Payne. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 12.02.2021.

Références

J Infect Dis. 2013 Apr;207(7):1058-65
pubmed: 23300161
Emerg Infect Dis. 2011 Aug;17(8):1381-8
pubmed: 21801613
Clin Diagn Lab Immunol. 1996 Jul;3(4):477-9
pubmed: 8807217
Clin Infect Dis. 2011 Feb 15;52(4):466-74
pubmed: 21258098
Clin Infect Dis. 2014 Feb;58(4):483-91
pubmed: 24300042
Rev Panam Salud Publica. 2000 Nov;8(5):305-31
pubmed: 11190969
PLoS One. 2014 May 05;9(5):e96674
pubmed: 24797911
Clin Infect Dis. 2019 Jul 2;69(2):357-365
pubmed: 30753367
J Biomed Inform. 2019 Jul;95:103208
pubmed: 31078660
Bull World Health Organ. 1995;73(6):793-8
pubmed: 8907773
J Pediatr Gastroenterol Nutr. 2013 Oct;57(4):514-9
pubmed: 23676445
N Engl J Med. 2009 Feb 5;360(6):588-98
pubmed: 19196675
N Engl J Med. 2013 Mar 21;368(12):1121-30
pubmed: 23514289
Rev Infect Dis. 1991 May-Jun;13 Suppl 6:S454-62
pubmed: 1862276
J Biomed Inform. 2009 Apr;42(2):377-81
pubmed: 18929686
Pediatr Infect Dis J. 2008 Mar;27(3):207-12
pubmed: 18277934
J Infect Dis. 1976 Sep;134(3):211-7
pubmed: 977992
Emerg Infect Dis. 2011 Jan;17(1):16-22
pubmed: 21192849
JAMA Pediatr. 2016 Sep 1;170(9):829-30
pubmed: 27366973
Clin Infect Dis. 2014 Feb;58(4):492-4
pubmed: 24300039
Clin Infect Dis. 2016 Jan 1;62(1):11-18
pubmed: 26508510
J Med Virol. 1981;7(4):263-71
pubmed: 7038043
Science. 2014 Nov 7;346(6210):755-9
pubmed: 25378626
Bull World Health Organ. 2015 Jan 1;93(1):19-28
pubmed: 25558104
J Infect Dis. 2020 Oct 13;222(10):1731-1739
pubmed: 32095831
Clin Vaccine Immunol. 2015 Aug;22(8):923-9
pubmed: 26041041
Lancet Infect Dis. 2002 Jan;2(1):25-32
pubmed: 11892493
Clin Infect Dis. 2015 Jun 1;60(11):1631-8
pubmed: 25744498
J Infect Dis. 2014 Nov 15;210(10):1582-9
pubmed: 24903663
JAMA Pediatr. 2020 Apr 1;174(4):383-385
pubmed: 31961393
Commun Dis Intell Q Rep. 2011 Jun;35(2):177-84
pubmed: 22010512
Bull World Health Organ. 2008 Sep;86(9):710-7
pubmed: 18797647
Epidemiology. 2007 Nov;18(6):800-4
pubmed: 18049194
Pediatrics. 2004 Jun;113(6):1758-64
pubmed: 15173503
J Pediatr. 1981 May;98(5):708-15
pubmed: 7229749
N Engl J Med. 1996 Oct 3;335(14):1022-8
pubmed: 8793926
Rev Infect Dis. 1989 May-Jun;11(3):498-505
pubmed: 2665005

Auteurs

Ardythe L Morrow (AL)

Department of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Mary A Staat (MA)

Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Emily A DeFranco (EA)

Department of Obstetrics and Gynecology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Monica M McNeal (MM)

Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Allison R Cline (AR)

Department of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Shannon C Conrey (SC)

Department of Environmental and Public Health Sciences, Division of Epidemiology, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.

Elizabeth P Schlaudecker (EP)

Division of Infectious Diseases, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Alexandra M Piasecki (AM)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Rachel M Burke (RM)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Liang Niu (L)

Department of Environmental and Public Health Sciences, Division of Biostatistics and Bioinformatics, University of Cincinnati College of Medicine, Cincinnati, OH, United States.

Aron J Hall (AJ)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Michael D Bowen (MD)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Susan I Gerber (SI)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Gayle E Langley (GE)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Natalie J Thornburg (NJ)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Angela P Campbell (AP)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Jan Vinjé (J)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Umesh D Parashar (UD)

Division of Viral Diseases, National Center for Immunization and Respiratory Disease, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Daniel C Payne (DC)

Division of Foodborne, Waterborne, and Environmental Diseases, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, United States.

Classifications MeSH