Literature DB >> 7706729

Representation of rearranged VH gene segments in the human adult antibody repertoire.

I Suzuki1, L Pfister, A Glas, C Nottenburg, E C Milner.   

Abstract

The heavy chain variable region composition of the human adult Ab repertoire is poorly defined, but recent evidence suggests that peripheral blood B cells may express a nonstochastic assortment of VH genes. In this study, the contribution of individual VH gene segments to the human Ab repertoire has been assessed. As a measure of VH gene utilization, the frequency of occurrence of eight individual VH3 gene segments contained in rearrangements was assessed in the peripheral blood B cells of two adult subjects. In addition, the frequency of occurrence of rearrangements containing nine individual VH4 gene segments was analyzed in one of the subjects. More than 2500 independent rearrangements were analyzed. For controls, amplifications and subsequent identification of nonrearranged VH3 and VH4 genes from the same individuals were also performed. The results of this germ-line analysis indicated that approximately 25 VH3 gene segments and nine VH4 gene segments could be amplified quantitatively. However, usage of elements was not uniform; one VH3 element, V3-23, and one VH4 element, V4-34, were represented among rearrangements more frequently than were other members of their respective families. This pattern of VH utilization was apparent in B cells isolated from the same subject after an 8-mo interval, indicating the relative stability of the repertoire over time. These results indicate that the adult human Ab repertoire is dominated by a few VH genes demonstrating a pattern of nonrandom utilization that could involve preferential rearrangement and/or receptor-dependent selection.

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Year:  1995        PMID: 7706729

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


  25 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-28       Impact factor: 11.205

2.  General strategy for the generation of human antibody variable domains with increased aggregation resistance.

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Journal:  Immunogenetics       Date:  2005-10-18       Impact factor: 2.846

4.  No evidence for the use of DIR, D-D fusions, chromosome 15 open reading frames or VH replacement in the peripheral repertoire was found on application of an improved algorithm, JointML, to 6329 human immunoglobulin H rearrangements.

Authors:  Line Ohm-Laursen; Morten Nielsen; Stine R Larsen; Torben Barington
Journal:  Immunology       Date:  2006-10       Impact factor: 7.397

5.  Similarities and differences between the light and heavy chain Ig variable region gene repertoires in chronic lymphocytic leukemia.

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Journal:  Mol Med       Date:  2006 Nov-Dec       Impact factor: 6.354

Review 6.  VH-mediated mechanisms in normal and neoplastic B cell development.

Authors:  L E Silberstein; S P Rao
Journal:  Immunol Res       Date:  1998       Impact factor: 2.829

7.  Analysis of the human VH gene repertoire. Differential effects of selection and somatic hypermutation on human peripheral CD5(+)/IgM+ and CD5(-)/IgM+ B cells.

Authors:  H P Brezinschek; S J Foster; R I Brezinschek; T Dörner; R Domiati-Saad; P E Lipsky
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Journal:  Blood       Date:  2017-01-11       Impact factor: 22.113

9.  Clonally-related immunoglobulin VH domains and nonrandom use of DH gene segments in rheumatoid arthritis synovium.

Authors:  B E Clausen; S L Bridges; J C Lavelle; P G Fowler; S Gay; W J Koopman; H W Schroeder
Journal:  Mol Med       Date:  1998-04       Impact factor: 6.354

10.  Recombinant monoclonal thyrotropin-stimulation blocking antibody (TSBAb) established from peripheral lymphocytes of a hypothyroid patient with primary myxedema.

Authors:  K Moriyama; J Okuda; M Saijo; Y Hattori; N Kanamoto; Y Hataya; F Matsuda; T Mori; K Nakao; T Akamizu
Journal:  J Endocrinol Invest       Date:  2003-11       Impact factor: 4.256

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