Literature DB >> 3493076

Analysis of somatic mutation and class switching in naive and memory B cells generating adoptive primary and secondary responses.

M Siekevitz, C Kocks, K Rajewsky, R Dildrop.   

Abstract

Clonal progeny of naive B cells (producing a primary antibody response) and of memory B cells (producing a secondary response) were identified in a cell transfer system. Primary response clones are typically derived from IgM precursors and express unmutated V regions. Multiple isotype switches occur in these clones. Secondary response clones derive from IgG1 precursors and express highly mutated V regions. Additional switches do not occur. With one exception, there was no evidence for somatic mutation during clonal expansion. The generation of mutated memory cells may thus represent a distinct differentiation pathway. Evidence is presented that, in this pathway, mutants that have lost antigen binding specificity but that remain available for stimulation by a different antigen arise upon antigenic stimulation.

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Year:  1987        PMID: 3493076     DOI: 10.1016/0092-8674(87)90073-0

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  60 in total

1.  Comparative T cell receptor repertoire selection by antigen after adoptive transfer: a glimpse at an antigen-specific preimmune repertoire.

Authors:  V Attuil; P Bucher; M Rossi; M Mutin; J L Maryanski
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-18       Impact factor: 11.205

2.  Boundaries of somatic mutation in rearranged immunoglobulin genes: 5' boundary is near the promoter, and 3' boundary is approximately 1 kb from V(D)J gene.

Authors:  S G Lebecque; P J Gearhart
Journal:  J Exp Med       Date:  1990-12-01       Impact factor: 14.307

3.  Distribution of mutations around rearranged heavy-chain antibody variable-region genes.

Authors:  G W Both; L Taylor; J W Pollard; E J Steele
Journal:  Mol Cell Biol       Date:  1990-10       Impact factor: 4.272

4.  Polyclonal B-cell expansion in the cerebrospinal fluid of patients with pseudotumor cerebri.

Authors:  Reng-Rong Da; Grace Kao; Wen-Zhong Guo; Michael Olek; Sudhir Gupta; Yiping Zhang; Stanley Van Den Noort; Yufen Qin
Journal:  J Clin Immunol       Date:  2004-11       Impact factor: 8.317

5.  Naive T-cell receptor transgenic T cells help memory B cells produce antibody.

Authors:  Darragh Duffy; Chun-Ping Yang; Andrew Heath; Paul Garside; Eric B Bell
Journal:  Immunology       Date:  2006-11       Impact factor: 7.397

6.  Mutation and selection during the secondary response to 2-phenyloxazolone.

Authors:  C Rada; S K Gupta; E Gherardi; C Milstein
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

7.  Both mutated and unmutated memory B cells accumulate mutations in the course of the secondary response and develop a new antibody repertoire optimally adapted to the secondary stimulus.

Authors:  Tomohiro Kaji; Koji Furukawa; Akiko Ishige; Itsumi Toyokura; Masaki Nomura; Mariko Okada; Yoshimasa Takahashi; Michiko Shimoda; Toshitada Takemori
Journal:  Int Immunol       Date:  2013-09-10       Impact factor: 4.823

8.  II. Correlations between secondary structure stability and mutation frequency during somatic hypermutation.

Authors:  Barbara E Wright; Karen H Schmidt; Nick Davis; Aaron T Hunt; Michael F Minnick
Journal:  Mol Immunol       Date:  2008-06-26       Impact factor: 4.407

9.  Clonal expansion and somatic hypermutation of V(H) genes of B cells from cerebrospinal fluid in multiple sclerosis.

Authors:  Y Qin; P Duquette; Y Zhang; P Talbot; R Poole; J Antel
Journal:  J Clin Invest       Date:  1998-09-01       Impact factor: 14.808

10.  Somatic hypermutation of the new antigen receptor gene (NAR) in the nurse shark does not generate the repertoire: possible role in antigen-driven reactions in the absence of germinal centers.

Authors:  M Diaz; A S Greenberg; M F Flajnik
Journal:  Proc Natl Acad Sci U S A       Date:  1998-11-24       Impact factor: 11.205

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