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Comprehensive analysis and selection of anthrax vaccine adsorbed immune correlates of protection in rhesus macaques.
Chen, Ligong; Schiffer, Jarad M; Dalton, Shannon; Sabourin, Carol L; Niemuth, Nancy A; Plikaytis, Brian D; Quinn, Conrad P.
Affiliation
  • Chen L; Centers for Disease Control and Prevention, Atlanta, Georgia, USA Atlanta Research and Education Foundation, Inc., Decatur, Georgia, USA.
  • Schiffer JM; Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Dalton S; Centers for Disease Control and Prevention, Atlanta, Georgia, USA Atlanta Research and Education Foundation, Inc., Decatur, Georgia, USA.
  • Sabourin CL; Battelle, Columbus, Ohio, USA.
  • Niemuth NA; Battelle, Columbus, Ohio, USA.
  • Plikaytis BD; Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
  • Quinn CP; Centers for Disease Control and Prevention, Atlanta, Georgia, USA cquinn@cdc.gov.
Clin Vaccine Immunol ; 21(11): 1512-20, 2014 Nov.
Article in En | MEDLINE | ID: mdl-25185577
ABSTRACT
Humoral and cell-mediated immune correlates of protection (COP) for inhalation anthrax in a rhesus macaque (Macaca mulatta) model were determined. The immunological and survival data were from 114 vaccinated and 23 control animals exposed to Bacillus anthracis spores at 12, 30, or 52 months after the first vaccination. The vaccinated animals received a 3-dose intramuscular priming series (3-i.m.) of anthrax vaccine adsorbed (AVA) (BioThrax) at 0, 1, and 6 months. The immune responses were modulated by administering a range of vaccine dilutions. Together with the vaccine dilution dose and interval between the first vaccination and challenge, each of 80 immune response variables to anthrax toxin protective antigen (PA) at every available study time point was analyzed as a potential COP by logistic regression penalized by least absolute shrinkage and selection operator (LASSO) or elastic net. The anti-PA IgG level at the last available time point before challenge (last) and lymphocyte stimulation index (SI) at months 2 and 6 were identified consistently as a COP. Anti-PA IgG levels and lethal toxin neutralization activity (TNA) at months 6 and 7 (peak) and the frequency of gamma interferon (IFN-γ)-secreting cells at month 6 also had statistically significant positive correlations with survival. The ratio of interleukin 4 (IL-4) mRNA to IFN-γ mRNA at month 6 also had a statistically significant negative correlation with survival. TNA had lower accuracy as a COP than did anti-PA IgG response. Following the 3-i.m. priming with AVA, the anti-PA IgG responses at the time of exposure or at month 7 were practicable and accurate metrics for correlating vaccine-induced immunity with protection against inhalation anthrax.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Biomarkers / Anthrax Vaccines / Anthrax Type of study: Prognostic_studies Limits: Animals Language: En Journal: Clin Vaccine Immunol Journal subject: ALERGIA E IMUNOLOGIA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2014 Document type: Article Affiliation country: United States Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Biomarkers / Anthrax Vaccines / Anthrax Type of study: Prognostic_studies Limits: Animals Language: En Journal: Clin Vaccine Immunol Journal subject: ALERGIA E IMUNOLOGIA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2014 Document type: Article Affiliation country: United States Country of publication: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA