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Cell mediated immune responses following revaccination with an influenza A/H5N1 vaccine.
Mbawuike, Innocent N; Atmar, Robert L; Patel, Shital M; Corry, David B; Winokur, Patricia L; Brady, Rebecca C; Chen, Wilbur H; Edwards, Kathryn M; Creech, C Buddy; Walter, Emmanuel B; Frey, Sharon E; Belshe, Robert B; Goll, Johannes B; Hill, Heather; Keitel, Wendy A.
Afiliação
  • Mbawuike IN; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, United States.
  • Atmar RL; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, United States; Department of Medicine, Baylor College of Medicine, Houston, TX, United States. Electronic address: ratmar@bcm.edu.
  • Patel SM; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, United States; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • Corry DB; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
  • Winokur PL; Department of Internal Medicine, University of Iowa, Iowa City, IA, United States.
  • Brady RC; Gamble Program for Clinical Studies, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States.
  • Chen WH; Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, United States.
  • Edwards KM; Vanderbilt Vaccine Research Program, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, United States.
  • Creech CB; Vanderbilt Vaccine Research Program, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN, United States.
  • Walter EB; Duke Clinical Vaccine Unit, Department of Pediatrics, Duke University School of Medicine, Durham, NC, United States.
  • Frey SE; Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Belshe RB; Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO, United States.
  • Goll JB; EMMES Corporation, Rockville, MD, United States.
  • Hill H; EMMES Corporation, Rockville, MD, United States.
  • Keitel WA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, United States; Department of Medicine, Baylor College of Medicine, Houston, TX, United States.
Vaccine ; 34(4): 547-554, 2016 Jan 20.
Article em En | MEDLINE | ID: mdl-26657997
ABSTRACT

PURPOSE:

The study aims were to determine whether inactivated influenza A/H5N1 vaccine administration elicited cell mediated immune (CMI) responses and the impact of adjuvant, vaccine dose and subject age on these responses.

METHODS:

Adults who were previously primed with either adjuvanted or unadjuvanted, inactivated, A/H5N1/Vietnam/1203/2004 (Clade 1) vaccine or unprimed (received placebo) in previous vaccine studies were randomized to receive one (primed) or two (unprimed) 15- or 90-mcg doses of inactivated, A/H5N1/Indonesia/05/05 (Clade 2) vaccine. Peripheral blood mononuclear cells (PBMCs) were collected and analyzed from a subset of vaccinees to assess CMI responses using IFN-γ and granzyme B ELISPOT assays. Cytokine measurements were performed on PBMC supernatants after stimulation with H5N1 virus.

RESULTS:

PBMCs were available from 177 participants; 88 and 89 received 15-mcg and 90-mcg of unadjuvanted clade 2 vaccine, respectively. Following H5N1 clade 1 stimulation, IFN-γ but not granzyme B normalized spot-forming cell numbers had statistically significant increased numbers at each of the post-vaccination timepoints compared to baseline in pooled analyses of all vaccine doses and age groups. Clade 2 stimulation resulted in statistically significant increased numbers of IFN-γ cells only 180 days following the last vaccination. Responses were similar among younger and older study participants, as were responses among those primed with alum-adjuvanted or non-adjuvanted clade 1 H5N1 vaccines. The dosage of clade 2 vaccine did not impact CMI responses among primed subjects, but responses were statistically significantly greater in unprimed recipients of the 90-mcg dosage compared to unprimed recipients of the 15-mcg dosage. IFN-γ levels in the supernatants of stimulated PBMC were strongly correlated with IFN-γ ELISPOT results.

CONCLUSION:

CMI responses occur in adults administered influenza A/H5N1 inactivated influenza vaccine.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Imunização Secundária / Influenza Humana / Imunidade Celular Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vacinas contra Influenza / Imunização Secundária / Influenza Humana / Imunidade Celular Idioma: En Ano de publicação: 2016 Tipo de documento: Article