Published online
doi:10.1084/jem.20071555
The Journal of Experimental Medicine, Vol. 205, No. 6, 1331-1342
The Rockefeller University Press, 0022-1007 $30.00
© Weller et al.
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 Picard2,4,
Corinne Cordier3,
Damiana Lecoeuche1,
Frédéric Gauthier5,
Jean-Claude Weill1, and
Claude-Agnès Reynaud1
1 Institut National de la Santé et de la Recherche Médicale (INSERM) U783, Développement du Système Immunitaire, 2 INSERM U550, Génétique des maladies infectieuses, 3 INSERM IFR 94, Service commun de Tri cellulaire, Université Paris Descartes, Faculté de Médecine, Site Necker Enfants-Malades, Paris 75015, France
4 Centre d'étude des déficits immunitaires, Hôpital Necker Enfants-Malades, Paris 75015, France
5 Service de Chirurgie Pédiatrique, Hôpital Bicêtre, Le Kremlin Bicêtre 94270, France
CORRESPONDENCE Jean-Claude Weill: weill{at}necker.fr OR Claude-Agnès Reynaud: reynaud{at}necker.fr
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 µ 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.
Abbreviations used: AID, activation-induced cytidine deaminase; GC, germinal center; MZ, marginal zone; SMZ, splenic MZ; TD, T-dependent; TI, T cell–independent.
© 2008 Weller et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jgp.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

CiteULike
Complore
Connotea
Del.icio.us
Digg
Facebook
Reddit
Technorati
Twitter What's this?
Related Article
-
Sheepish B cells: evidence for antigen-independent antibody diversification in humans and mice
- David Tarlinton
J. Exp. Med. 2008 205: 1251-1254.
[Abstract]
[Full Text]
[PDF]
This article has been cited by other articles:
-
Kuraoka, M., Liao, D., Yang, K., Allgood, S. D., Levesque, M. C., Kelsoe, G., Ueda, Y.
(2009). Activation-Induced Cytidine Deaminase Expression and Activity in the Absence of Germinal Centers: Insights into Hyper-IgM Syndrome. J. Immunol.
183: 3237-3248
[Abstract]
[Full Text]
-
Bende, R. J., van Maldegem, F., van Noesel, C. J.M.
(2009). Chronic inflammatory disease, lymphoid tissue neogenesis and extranodal marginal zone B-cell lymphomas. haematol
94: 1109-1123
[Abstract]
[Full Text]
-
Faili, A., Stary, A., Delbos, F., Weller, S., Aoufouchi, S., Sarasin, A., Weill, J.-C., Reynaud, C.-A.
(2009). A Backup Role of DNA Polymerase {kappa} in Ig Gene Hypermutation Only Takes Place in the Complete Absence of DNA Polymerase {eta}. J. Immunol.
182: 6353-6359
[Abstract]
[Full Text]