Unbound MEDLINE

Allogeneic hematopoietic stem cell transplantation recipients have defects of both switched and igm memory B cells. Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation [Biol Blood Marrow Transplant] Journal article

 
TitleAllogeneic hematopoietic stem cell transplantation recipients have defects of both switched and igm memory B cells.
Author(s)D'Orsogna LJ, Wright MP, Krueger RG, McKinnon EJ, Buffery SI, Witt CS, Staples N, Loh R, Cannell PK, Christiansen FT, French MA 
InstitutionDepartment of Clinical Immunology and Immunogenetics, Royal Perth Hospital and PathWest Laboratory Medicine, Perth, Australia.
SourceBiol Blood Marrow Transplant 2009 Jul; 15(7):795-803.
MeSHAdult
Antibodies, Bacterial
Antigens, CD19
Antigens, CD27
B-Lymphocytes
CD4-Positive T-Lymphocytes
Cross-Sectional Studies
Female
Gene Rearrangement, B-Lymphocyte
Graft vs Host Disease
Hematopoietic Stem Cell Transplantation
Humans
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M
Immunologic Memory
Male
Middle Aged
Polysaccharides, Bacterial
Retrospective Studies
Streptococcus pneumoniae
Transplantation, Homologous
AbstractAllogeneic hematopoietic stem cell transplant (HSCT) recipients were assessed to elucidate memory B cell defects underlying their increased susceptibility to infections, particularly by encapsulated bacteria. Circulating IgM memory B cells (CD19+, CD27+, IgM+) and switched memory B cells (CD19+, CD27+, IgM(-)) were enumerated in allogeneic HSCT recipients (n = 37) and healthy controls (n = 35). T lymphocyte subpopulations and serum levels of immunoglobulins, including IgG subclasses, and antibodies to pneumococcal polysaccharides were also assayed. Allogeneic HSCT recipients were deficient in both switched memory and IgM memory B cells compared to healthy controls (both P < .0001), irrespective of time post-HSCT. Switched memory B cell deficiency correlated with CD4+ T cell deficiency, and both correlated with serum levels of IgG1 (P < .0001), possibly reflecting impaired B cell isotype switching in germinal centres. "Steady-state" serum levels of antibodies to pneumococcal polysaccharides did not correlate with circulating memory B cells. Graft-versus-host disease (GVHD) was associated with lower IgM memory B cell counts and lower serum levels of IgG2, IgG4, IgA, and pneumococcal antibodies. The increased susceptibility of allogeneic HSCT patients to infection may reflect a combination of memory B cell defects, which are most common in patients with a history of GVHD.
Languageeng
Pub Type(s)Comparative Study
Journal Article
PubMed ID19539210
  
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