Functional T-cell deficiency in adolescents who experience serogroup C meningococcal disease despite receiving the meningococcal serogroup C conjugate vaccine
Functional T-cell deficiency in adolescents who experience serogroup C meningococcal disease despite receiving the meningococcal serogroup C conjugate vaccine
Some individuals have experienced meningococcal disease despite receiving the meningococcal serogroup C conjugate (MCC) vaccine in adolescence. We sought to determine whether this is due to subclinical functional B- or T-cell immunodeficiency. Of 53 vaccine failures identified by enhanced surveillance of England and Wales from 1999 to 2004, 15 received MCC vaccine in adolescence, 9 of whom were recruited 2 to 6 years following convalescence from meningococcal disease. Their peripheral blood mononuclear cells (PBMCs) were incubated with polyclonal activators designed to mimic T-cell-independent B-cell stimulation by bacterial polysaccharides and the T-cell stimulation provided by the protein component of the conjugate vaccine. Subsequent proliferation and activation of T and B lymphocytes were measured, along with T-cell help to B cells. Compared to age-, sex-, geographically, and ethnicity-matched controls, CD4 T-cell proliferation rates in response to both anti-CD3 (T-cell receptor [TCR]) stimulation and anti-CD3 in the presence of B cells activated through anti-IgD conjugated to dextran (alpha-delta-dex) were lower in PBMCs derived from vaccine failures (P = 0.044 and P = 0.029, respectively). There was reduced CD4 cell activation of the patient cells compared to controls following stimulation by CD3 (P = 0.048). B-cell activation during incubation of PBMCs with the T-cell stimuli, anti-CD3 (P = 0.044), or anti-CD3 plus anti-CD28 (P = 0.018) was relatively impaired in patients. Anti-tetanus toxoid IgG concentrations were lower in the vaccine failure group (P = 0.0385). There was a relative defect of T-cell responsiveness to T-cell-dependent antigen stimulation in MCC vaccine failures, which was manifested in reduced T-cell help to B cells.
1104-1110
Foster, Rachel A.
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Carlring, Jennifer
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Lees, Andrew
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Borrow, Ray
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Ramsay, Mary
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Kacsmarski, Ed
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Miller, Elizabeth
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McKendrick, Michael W.
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Heath, Andrew W.
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Read, Robert C.
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July 2010
Foster, Rachel A.
ae78b2b5-6fee-486e-ac49-b755d2d2314c
Carlring, Jennifer
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Lees, Andrew
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Borrow, Ray
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Ramsay, Mary
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Kacsmarski, Ed
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Miller, Elizabeth
180cf79e-2de5-4cc4-bba4-c1610d5b5036
McKendrick, Michael W.
91cf7c85-c506-466c-a04f-2d9e2c60a2b7
Heath, Andrew W.
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Read, Robert C.
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Foster, Rachel A., Carlring, Jennifer, Lees, Andrew, Borrow, Ray, Ramsay, Mary, Kacsmarski, Ed, Miller, Elizabeth, McKendrick, Michael W., Heath, Andrew W. and Read, Robert C.
(2010)
Functional T-cell deficiency in adolescents who experience serogroup C meningococcal disease despite receiving the meningococcal serogroup C conjugate vaccine.
Clinical and Vaccine Immunology, 17 (7), .
(doi:10.1128/CVI.00481-09).
(PMID:20463106)
Abstract
Some individuals have experienced meningococcal disease despite receiving the meningococcal serogroup C conjugate (MCC) vaccine in adolescence. We sought to determine whether this is due to subclinical functional B- or T-cell immunodeficiency. Of 53 vaccine failures identified by enhanced surveillance of England and Wales from 1999 to 2004, 15 received MCC vaccine in adolescence, 9 of whom were recruited 2 to 6 years following convalescence from meningococcal disease. Their peripheral blood mononuclear cells (PBMCs) were incubated with polyclonal activators designed to mimic T-cell-independent B-cell stimulation by bacterial polysaccharides and the T-cell stimulation provided by the protein component of the conjugate vaccine. Subsequent proliferation and activation of T and B lymphocytes were measured, along with T-cell help to B cells. Compared to age-, sex-, geographically, and ethnicity-matched controls, CD4 T-cell proliferation rates in response to both anti-CD3 (T-cell receptor [TCR]) stimulation and anti-CD3 in the presence of B cells activated through anti-IgD conjugated to dextran (alpha-delta-dex) were lower in PBMCs derived from vaccine failures (P = 0.044 and P = 0.029, respectively). There was reduced CD4 cell activation of the patient cells compared to controls following stimulation by CD3 (P = 0.048). B-cell activation during incubation of PBMCs with the T-cell stimuli, anti-CD3 (P = 0.044), or anti-CD3 plus anti-CD28 (P = 0.018) was relatively impaired in patients. Anti-tetanus toxoid IgG concentrations were lower in the vaccine failure group (P = 0.0385). There was a relative defect of T-cell responsiveness to T-cell-dependent antigen stimulation in MCC vaccine failures, which was manifested in reduced T-cell help to B cells.
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e-pub ahead of print date: 12 May 2010
Published date: July 2010
Organisations:
Clinical & Experimental Sciences
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Local EPrints ID: 346782
URI: http://eprints.soton.ac.uk/id/eprint/346782
ISSN: 1556-6811
PURE UUID: ef5f2f4c-bdd2-41a0-a52f-5194da10188c
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Date deposited: 09 Jan 2013 12:39
Last modified: 15 Mar 2024 03:42
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Author:
Rachel A. Foster
Author:
Jennifer Carlring
Author:
Andrew Lees
Author:
Ray Borrow
Author:
Mary Ramsay
Author:
Ed Kacsmarski
Author:
Elizabeth Miller
Author:
Michael W. McKendrick
Author:
Andrew W. Heath
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