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Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infants.
Weller S., Mamani-Matsuda M., Picard C., Cordier C., Lecoeuche D., Gauthier F., Weill J.-C., Reynaud C.-A.
Journal of Experimental Medicine / The Journal of Experimental Medicine 205, 6 (2008) 1331-42 - http://www.hal.inserm.fr/inserm-00331378
 (18519648) 
Somatic diversification in the absence of antigen-driven responses is the hallmark of the IgM+ IgD+ CD27+ B cell repertoire in infants.
Sandra Weller1, Maria Mamani-Matsuda1, Capucine Picard2, 3, Corinne Cordier4, Damiana Lecoeuche1, Frédéric Gauthier5, Jean-Claude Weill () 1, Claude-Agnès Reynaud () 1
1 :  Developpement du Systeme Immunitaire
INSERM : U783 – Université Paris V - Paris Descartes
Fac de Medecine Necker-Enfants Malades PARIS V 156, Rue de Vaugirard 75730 PARIS CEDEX 15
France
2 :  Génétique Humaine des Maladies Infectieuses
INSERM : U550 – Université Paris V - Paris Descartes
Fac de Medecine Necker-Enfants Malades 156, Rue de Vaugirard 75730 PARIS CEDEX 15
France
3 :  CEREDIH - Centre de Référence Déficits Immunitaires Héréditaires
http://www.ceredih.fr/
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Necker - Enfants Malades
149, rue de Sevres 75015 PARIS
France
4 :  IRNEM - IFR Necker-Enfants Malades
http://www.necker.fr/irnem
INSERM : IFR94 – CNRS : IFR94 – Assistance publique - Hôpitaux de Paris (AP-HP) – Université Paris V - Paris Descartes
GH Necker - Enfants Malades 149, Rue de Sevres 75743 PARIS CEDEX 15
France
5 :  Service de chirurgie pédiatrique
Assistance publique - Hôpitaux de Paris (AP-HP) – Hôpital Bicêtre
Le Kremlin-Bicêtre
France
T cell-dependent immune responses develop soon after birth, whereas it takes 2 yr for humans to develop T cell-independent responses. We used this dissociation to analyze the repertoire diversification of IgM(+)IgD(+)CD27(+) B cells (also known as "IgM memory" B cells), comparing these cells with switched B cells in children <2 yr of age, with the aim of determining whether these two subsets are developmentally related. We show that the repertoire of IgM(+)IgD(+)CD27(+) B cells in the spleen and blood displays no sign of antigen-driven activation and expansion on H-CDR3 spectratyping, despite the many antigenic challenges provided by childhood vaccinations. This repertoire differed markedly from those of switched B cells and splenic germinal center B cells, even at the early stage of differentiation associated with mu heavy chain expression. These data provide evidence for the developmental diversification of IgM(+)IgD(+)CD27(+) B cells, at least in very young children, outside of T cell-dependent and -independent immune responses.
Sciences du Vivant/Immunologie
Anglais
0022-1007

Articles dans des revues avec comité de lecture
10.1084/jem.20071555
Journal of Experimental Medicine / The Journal of Experimental Medicine
internationale
09/06/2008
02/06/2008
205
6
1331-42

"somatic hypermutation" – "splenic marginal zone" – "Ig repertoire"
Antigens – CD – Antigens – CD27 – B-Lymphocyte Subsets – B-Lymphocytes – Gene Rearrangement – Humans – Immunoglobulin D – Immunoglobulin M – Immunoglobulin Variable Region – Immunoglobulin mu-Chains – Immunologic Memory – Infant – Lymphocyte Activation – Spleen – T-Lymphocytes – Transcription – Genetic – Variation (Genetics)
Ligue Nationale contre le Cancer
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