Federico Martinón-Torres1, Jacek Wysocki, Kimberly J Center, Hanna Czajka, Ewa Majda-Stanislawska, Felix Omeñaca, Ana Concheiro-Guisan, Francisco Gimenez-Sanchez, Leszek Szenborn, Daniel Blázquez-Gamero, Laura Moreno-Galarraga, Peter C Giardina, Gang Sun, William C Gruber, Daniel A Scott, Alejandra Gurtman. 1. From the *Translational Pediatrics and Infectious Diseases, Pediatrics Department, Hospital Clínico Universitario de Santiago de Compostela and Vaccine Research Unit, Genetics, Vaccines, Infections and Pediatrics Research Group (GENVIP), Healthcare Research Institute of Santiago, Santiago de Compostela, Spain; †Department of Preventive Medicine, Poznań University of Medical Sciences, Poznań, Poland; ‡Vaccine Research, Pfizer Inc, Collegeville, Pennsylvania; §Department of Infectious Diseases, Infectious Diseases Outpatient Clinic, Kraków, Poland; ¶Department of Pediatric Infectious Diseases, Medical University of Łódź, Łódź, Poland; ‖Sección Servicio Neonatología, Hospital Infantil La Paz, Madrid, Spain; **Departamento Pediatria, Complexo Hospitalario Universitario de Vigo, Vigo, Spain; ††Pediatrics Department, Hospital Torrecardenas, Almeria, and Balmis Institute of Vaccines, Spain; ‡‡Department of Pediatric Infectious Diseases, Medical University, Wrocław, Poland; §§Pediatric Infectious Diseases and Immunodeficiencies Unit, Hospital Universitario 12 de Octubre, Madrid, Spain; ¶¶Pediatrics Department, Vaccine Research Unit, Fundación Miguel Servet, Complejo Hospitalario de Navarra, IdiSNA, Pamplona, Spain; ‖‖Vaccine Research, Pfizer Inc, Pearl River, New York; and ***Biostatistics, PBU in Ventiv Health Clinical, LLC, Princeton, New Jersey.
Abstract
BACKGROUND: Premature infants have lower short-term immune responses to vaccination than term infants, but patterns of antibody persistence in preterm infants over longer periods are not well established. This study assessed the persistence of antibody response to the 13-valent pneumococcal conjugate vaccine (PCV13) in formerly preterm versus term infants. METHODS: In total, 100 preterm and 100 term infants received PCV13 with routine vaccines at ages 2, 3, 4 and 12 months. Serotype-specific anticapsular immunoglobulin G (IgG)-binding antibodies and opsonophagocytic activity were determined 1 and 2 years after the last PCV13 dose. RESULTS: At 1 and 2 years after the last vaccination (toddler dose), IgG geometric mean concentrations (GMCs) for all serotypes had declined from levels measured 1 month after the toddler dose but remained above pretoddler dose levels. IgG GMCs were significantly lower in preterm than term subjects for a majority of serotypes at both follow-up time points. IgG GMCs increased in both groups for some serotypes from the 1-year to 2-year follow-up, whereas others declined. Opsonophagocytic activity results supported the IgG results. CONCLUSIONS: The routine (3 + 1) vaccination schedule is likely to offer long-term protection against invasive pneumococcal disease in preterm infants and should be initiated regardless of gestational age or weight at birth, without delay of the toddler dose.
BACKGROUND: Premature infants have lower short-term immune responses to vaccination than term infants, but patterns of antibody persistence in preterm infants over longer periods are not well established. This study assessed the persistence of antibody response to the 13-valent pneumococcal conjugate vaccine (PCV13) in formerly preterm versus term infants. METHODS: In total, 100 preterm and 100 term infants received PCV13 with routine vaccines at ages 2, 3, 4 and 12 months. Serotype-specific anticapsular immunoglobulin G (IgG)-binding antibodies and opsonophagocytic activity were determined 1 and 2 years after the last PCV13 dose. RESULTS: At 1 and 2 years after the last vaccination (toddler dose), IgG geometric mean concentrations (GMCs) for all serotypes had declined from levels measured 1 month after the toddler dose but remained above pretoddler dose levels. IgG GMCs were significantly lower in preterm than term subjects for a majority of serotypes at both follow-up time points. IgG GMCs increased in both groups for some serotypes from the 1-year to 2-year follow-up, whereas others declined. Opsonophagocytic activity results supported the IgG results. CONCLUSIONS: The routine (3 + 1) vaccination schedule is likely to offer long-term protection against invasive pneumococcal disease in preterm infants and should be initiated regardless of gestational age or weight at birth, without delay of the toddler dose.
Authors: Deborah Lehmann; Wendy Kirarock; Anita H J van den Biggelaar; Megan Passey; Peter Jacoby; Gerard Saleu; Geraldine Masiria; Birunu Nivio; Andrew Greenhill; Tilda Orami; Jacinta Francis; Rebecca Ford; Lea-Ann Kirkham; Vela Solomon; Peter C Richmond; William S Pomat Journal: Pneumonia (Nathan) Date: 2017-12-25
Authors: Ángela Domínguez; Pilar Ciruela; Sergi Hernández; Juan José García-García; Núria Soldevila; Conchita Izquierdo; Fernando Moraga-Llop; Alvaro Díaz; Mariona F de Sevilla; Sebastià González-Peris; Magda Campins; Sonia Uriona; Johanna Martínez-Osorio; Anna Solé-Ribalta; Gemma Codina; Cristina Esteva; Ana María Planes; Carmen Muñoz-Almagro; Luis Salleras Journal: PLoS One Date: 2017-08-14 Impact factor: 3.240