The anti-(4-hydroxy-3-nitro-phenyl)acetyl (NP) response is dominated by lambda 1 chain-bearing antibodies expressing the VH gene V186.2 in combination with the D element DFL16.1. lambda 1-positive B cells were isolated from the spleens of mice immunized with NP-chicken gamma globulin 6 wk earlier. Rearranged V186.2 genes were amplified from the genomic DNA of these cells and sequenced. In cases where the rearrangement was typical for secondary anti-NP antibodies, the VHDJH sequences were generally heavily mutated. The frequency and the nature of the nucleotide exchanges mirrored those of secondary response antibodies. V186.2 genes with other rearrangements and V186.2-related genes isolated concomitantly were essentially unmutated. These results demonstrate: (a) that somatic antibody mutants are largely restricted to a small compartment of peripheral B cells, namely, that of memory cells; (b) that the memory compartment is strongly selected for high affinity precursors and largely purged from antigen-binding loss mutants; and (c) that the repertoire of binding specificities expressed in the secondary response is established in its final form before secondary immunization.
Skip Nav Destination
Article navigation
1 December 1990
Article|
December 01 1990
The repertoire of somatic antibody mutants accumulating in the memory compartment after primary immunization is restricted through affinity maturation and mirrors that expressed in the secondary response.
U Weiss,
U Weiss
Institute for Genetics, University of Cologne, FRG.
Search for other works by this author on:
K Rajewsky
K Rajewsky
Institute for Genetics, University of Cologne, FRG.
Search for other works by this author on:
U Weiss
,
K Rajewsky
Institute for Genetics, University of Cologne, FRG.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1990) 172 (6): 1681–1689.
Citation
U Weiss, K Rajewsky; The repertoire of somatic antibody mutants accumulating in the memory compartment after primary immunization is restricted through affinity maturation and mirrors that expressed in the secondary response.. J Exp Med 1 December 1990; 172 (6): 1681–1689. doi: https://doi.org/10.1084/jem.172.6.1681
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement