Literature DB >> 8662073

New alleles of IGKV genes A2 and A18 suggest significant human IGKV locus polymorphism.

M J Atkinson1, M J Cowan, A J Feeney.   

Abstract

The human kappa light chain consists of approximately 35 potentially functional IGKV genes. However, an estimation of the diversity in the IGKV repertoire of an individual will be affected by the extent of polymorphisms for the different IGKV genes and their patterns of inheritance. To date, little information is available to indicate the extent of allelic variation of the IGKV genes. We examined the extent of allelism for one IGKV gene pair, the distal region A2 gene and its closely related proximal region duplicate A18. We found two new alleles for A2 and one new allele for A18, and sequenced approximately 1 kilobase flanking each gene. The new A18 allele, unlike the originally described allele, appears to be functional. All these alleles were found at relatively high frequencies in the four ethnic populations studied, with the exception of the defective A2b allele which was highly represented only in Navajos. The originally described A2a allele encodes for the predominant protective antibody against Haemophilus influenzae. Therefore, the patterns of allelic inheritance described for this IGKV gene pair indicate that allelism in the IGKV locus is likely to have a significant impact on immune responses.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8662073

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  9 in total

Review 1.  Factors that influence formation of B cell repertoire.

Authors:  A J Feeney
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

2.  Structural requirements of the major protective antibody to Haemophilus influenzae type b.

Authors:  L Hougs; L Juul; A Svejgaard; T Barington
Journal:  Infect Immun       Date:  1999-05       Impact factor: 3.441

3.  Polysaccharide binding potential of the human A2 or A18 kappa light chain homologues.

Authors:  D C Reason; T C Wagner; V R Tang; K D Moulton; A H Lucas
Journal:  Infect Immun       Date:  1999-02       Impact factor: 3.441

4.  Vkappa polymorphisms in NOD mice are spread throughout the entire immunoglobulin kappa locus and are shared by other autoimmune strains.

Authors:  Rachel A Henry; Peggy L Kendall; Emily J Woodward; Chrys Hulbert; James W Thomas
Journal:  Immunogenetics       Date:  2010-06-17       Impact factor: 2.846

5.  Human Fab fragments specific for the Haemophilus influenzae b polysaccharide isolated from a bacteriophage combinatorial library use variable region gene combinations and express an idiotype that mirrors in vivo expression.

Authors:  D C Reason; T C Wagner; A H Lucas
Journal:  Infect Immun       Date:  1997-01       Impact factor: 3.441

6.  Oligoclonality of serum immunoglobulin G antibody responses to Streptococcus pneumoniae capsular polysaccharide serotypes 6B, 14, and 23F.

Authors:  A H Lucas; D M Granoff; R E Mandrell; C C Connolly; A S Shan; D C Powers
Journal:  Infect Immun       Date:  1997-12       Impact factor: 3.441

7.  Divergent human populations show extensive shared IGK rearrangements in peripheral blood B cells.

Authors:  Katherine Jean Louise Jackson; Yan Wang; Bruno A Gaeta; William Pomat; Peter Siba; Janet Rimmer; William A Sewell; Andrew M Collins
Journal:  Immunogenetics       Date:  2011-07-26       Impact factor: 2.846

8.  The mouse antibody heavy chain repertoire is germline-focused and highly variable between inbred strains.

Authors:  Andrew M Collins; Yan Wang; Krishna M Roskin; Christopher P Marquis; Katherine J L Jackson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2015-09-05       Impact factor: 6.237

9.  The reported germline repertoire of human immunoglobulin kappa chain genes is relatively complete and accurate.

Authors:  Andrew M Collins; Yan Wang; Viveka Singh; Phillip Yu; Katherine J Jackson; William A Sewell
Journal:  Immunogenetics       Date:  2008-08-20       Impact factor: 2.846

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.