Literature DB >> 2230115

Development of B cell lineages during a primary anti-hapten immune response.

W Tao1, A L Bothwell.   

Abstract

Cell lineage relationships were examined in large numbers of hybridomas derived from a single mouse at 7 days and from a single mouse at 12 days after a primary immunization. The properties of these developing lineages provide unique insight into their biologic selection and differentiation. The unique VDJ junctions, the characteristics of the somatic mutations, and the nonproductive H chain gene rearrangements observed at day 12 all indicate that the hybridomas were derived from a limited number of progenitor B cells. Clonally related hybridomas were also observed at day 7. The activation of these lineages occurred very early, because somatic variants were strongly selected for within a few days after the primary immunization.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2230115

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  7 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-05-11       Impact factor: 16.971

2.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-04-11       Impact factor: 16.971

3.  Immunoglobulin class switching appears to be regulated by B-cell antigen receptor-specific T-cell action.

Authors:  Hans Lange; Oliver Hecht; Michael Zemlin; Ahmad Trad; Radu I Tanasa; Harry W Schroeder; Hilmar Lemke
Journal:  Eur J Immunol       Date:  2012-04       Impact factor: 5.532

4.  Somatic mutation in constant regions of mouse lambda 1 light chains.

Authors:  N Motoyama; H Okada; T Azuma
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-15       Impact factor: 11.205

5.  In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. II. A common clonal origin for periarteriolar lymphoid sheath-associated foci and germinal centers.

Authors:  J Jacob; G Kelsoe
Journal:  J Exp Med       Date:  1992-09-01       Impact factor: 14.307

6.  In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations.

Authors:  J Jacob; R Kassir; G Kelsoe
Journal:  J Exp Med       Date:  1991-05-01       Impact factor: 14.307

7.  In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. IV. Affinity-dependent, antigen-driven B cell apoptosis in germinal centers as a mechanism for maintaining self-tolerance.

Authors:  S Han; B Zheng; J Dal Porto; G Kelsoe
Journal:  J Exp Med       Date:  1995-12-01       Impact factor: 14.307

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.