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Human Nasal Challenge with Streptococcus pneumoniae Is Immunising in the Absence of Carriage

Title: Human Nasal Challenge with Streptococcus pneumoniae Is Immunising in the Absence of Carriage
Authors: Adam K. A. Wright; Daniela M. Ferreira; Jenna F. Gritzfeld; Angela D. Wright; Kathryn Armitage; Kondwani C. Jambo; Emily Bate; Sherouk El Batrawy; Andrea Collins; Stephen B. Gordon
Contributors: The Pennsylvania State University CiteSeerX Archives
Source: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/88/83/PLoS_Pathog_2012_Apr_5_8(4)_e1002622.tar.gz
Collection: CiteSeerX
Description: Infectious challenge of the human nasal mucosa elicits immune responses that determine the fate of the host-bacterial interaction; leading either to clearance, colonisation and/or disease. Persistent antigenic exposure from pneumococcal colonisation can induce both humoral and cellular defences that are protective against carriage and disease. We challenged healthy adults intra-nasally with live 23F or 6B Streptococcus pneumoniae in two sequential cohorts and collected nasal wash, bronchoalveolar lavage (BAL) and blood before and 6 weeks after challenge. We hypothesised that both cohorts would successfully become colonised but this did not occur except for one volunteer. The effect of bacterial challenge without colonisation in healthy adults has not been previously assessed. We measured the antigen-specific humoral and cellular immune responses in challenged but not colonised volunteers by ELISA and Flow Cytometry. Antigen-specific responses were seen in each compartment both before and after bacterial challenge for both cohorts. Antigen-specific IgG and IgA levels were significantly elevated in nasal wash 6 weeks after challenge compared to baseline. Immunoglobulin responses to pneumococci were directed towards various protein targets but not capsular polysaccharide. 23F but not 6B challenge elevated IgG anti-PspA in BAL. Serum immunoglobulins did not increase in response to challenge. In neither challenge cohort was there any alteration in the frequencies of TNF, IL-17 or IFNc producing CD4 T cells before or after challenge in BAL or blood. We show that simple, low dose mucosal exposure with pneumococci may immunise mucosal
Document Type: text
File Description: application/zip
Language: English
Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.271.1379
Availability: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.271.1379
Rights: Metadata may be used without restrictions as long as the oai identifier remains attached to it.
Accession Number: edsbas.6FFDF5EF
Database: BASE