Literature DB >> 28892455

Modeling specific antibody responses to natural immunization to predict a correlate of protection against infection before commencing a clinical vaccine trial.

Anthony Almudevar1, Michael E Pichichero2.   

Abstract

BACKGROUND: Clinical trials of vaccines for children to prevent acute otitis media (AOM) infections caused by the bacteria Streptococcus pneumonia (Spn) are in Phase I. The objective of this study was to use serum antibody measurements to pneumococcal purified protein candidate antigens that occurred after natural "immunization" to predict a correlate of protection response needed following an injectable vaccine against AOM in children.
METHODS: 590 nasal and serum samples were collected from 129 healthy children at 6, 9, 12, 15, 18, 24 and 30-36 months of age and when the child developed AOM. Middle ear fluid to detect Spn was collected at every episode of AOM. Quantitative ELISA was used to determine serum IgG against 7 Spn vaccine antigens: PspA clade 3, PspA clade 5, PhtD, PhtE, LytB, PcpA and Ply. A correlate of protection (COP) was estimated by regressing AOM events against age adjusted antibody levels induced by nasopharyngeal colonization and AOM infections, using logistic regression and generalized estimating equation methods.
RESULTS: A significant COP was found for Spn PhtD (p = 0.0015), PhtE (p = 0.00034), LytB (p = 0.004), PcpA (p = 0.002), and Ply (p = 0.007) between higher antibody levels and reduced frequency of AOM. We estimated that a 2-fold higher antibody level in a child than the mean antibody level induced by NP colonization (after adjusting for subject age) to PhtD, LytB, PcpA, PhtE or Ply reduced the risk of AOM by 14-21%, a 4-fold higher level reduced it by 25-38% and a 10-fold higher level reduced it by 39-54%.
CONCLUSION: We developed a model to predict the necessary level of serum antibody and fold higher above a threshold to PhtD, PhtE, LytB, PcpA and Ply that would correlate with a reduced likelihood of AOM in children age 6-24 months old if enrolled in a Phase III clinical efficacy trial.

Entities:  

Keywords:  Streptococcus pneumoniae; antibody response; nasopharyngeal colonization

Mesh:

Substances:

Year:  2017        PMID: 28892455      PMCID: PMC5647974          DOI: 10.1080/21645515.2017.1329064

Source DB:  PubMed          Journal:  Hum Vaccin Immunother        ISSN: 2164-5515            Impact factor:   3.452


  31 in total

Review 1.  Dynamics of nasopharyngeal colonization by potential respiratory pathogens.

Authors:  J A García-Rodríguez; M J Fresnadillo Martínez
Journal:  J Antimicrob Chemother       Date:  2002-12       Impact factor: 5.790

2.  When co-colonizing the nasopharynx haemophilus influenzae predominates over Streptococcus pneumoniae except serotype 19A strains to cause acute otitis media.

Authors:  Qingfu Xu; Janet R Casey; Arthur Chang; Michael E Pichichero
Journal:  Pediatr Infect Dis J       Date:  2012-06       Impact factor: 2.129

3.  Development of natural antibodies to pneumococcal surface protein A, pneumococcal surface adhesin A and pneumolysin in Filipino pregnant women and their infants in relation to pneumococcal carriage.

Authors:  Emma Holmlund; Beatriz Quiambao; Jukka Ollgren; Hanna Nohynek; Helena Käyhty
Journal:  Vaccine       Date:  2005-08-03       Impact factor: 3.641

4.  Correlation of higher antibody levels to pneumococcal proteins with protection from pneumococcal acute otitis media but not protection from nasopharyngeal colonization in young children.

Authors:  Q Xu; J R Casey; A Almudevar; M E Pichichero
Journal:  Clin Microbiol Infect       Date:  2017-01-28       Impact factor: 8.067

5.  Nasopharyngeal colonization elicits antibody responses to staphylococcal and pneumococcal proteins that are not associated with a reduced risk of subsequent carriage.

Authors:  Sabine M P J Prevaes; Willem J B van Wamel; Corné P de Vogel; Reinier H Veenhoven; Elske J M van Gils; Alex van Belkum; Elisabeth A M Sanders; Debby Bogaert
Journal:  Infect Immun       Date:  2012-03-26       Impact factor: 3.441

6.  Synchrony in serum antibody response to conserved proteins of Streptococcus pneumoniae in young children.

Authors:  Dabin Ren; Anthony L Almudevar; Michael E Pichichero
Journal:  Hum Vaccin Immunother       Date:  2015       Impact factor: 3.452

7.  Immunization of healthy adults with a single recombinant pneumococcal surface protein A (PspA) variant stimulates broadly cross-reactive antibodies to heterologous PspA molecules.

Authors:  G S Nabors; P A Braun; D J Herrmann; M L Heise; D J Pyle; S Gravenstein; M Schilling; L M Ferguson; S K Hollingshead; D E Briles; R S Becker
Journal:  Vaccine       Date:  2000-03-06       Impact factor: 3.641

8.  Emergence of a multiresistant serotype 19A pneumococcal strain not included in the 7-valent conjugate vaccine as an otopathogen in children.

Authors:  Michael E Pichichero; Janet R Casey
Journal:  JAMA       Date:  2007-10-17       Impact factor: 56.272

9.  Vaccination with a Streptococcus pneumoniae trivalent recombinant PcpA, PhtD and PlyD1 protein vaccine candidate protects against lethal pneumonia in an infant murine model.

Authors:  David Verhoeven; Qingfu Xu; Michael E Pichichero
Journal:  Vaccine       Date:  2014-04-13       Impact factor: 3.641

10.  Nasopharyngeal bacterial interactions in children.

Authors:  Qingfu Xu; Anthony Almudervar; Janet R Casey; Michael E Pichichero
Journal:  Emerg Infect Dis       Date:  2012-11       Impact factor: 6.883

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  1 in total

Review 1.  Panel 8: Vaccines and immunology.

Authors:  Mark R Alderson; Tim Murphy; Stephen I Pelton; Laura A Novotny; Laura L Hammitt; Arwa Kurabi; Jian-Dong Li; Ruth B Thornton; Lea-Ann S Kirkham
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2019-12-18       Impact factor: 1.675

  1 in total

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