Literature DB >> 1908881

Many variable region genes are utilized in the antibody response of BALB/c mice to the influenza virus A/PR/8/34 hemagglutinin.

A J Caton1, S E Stark, J Kavaler, L M Staudt, D Schwartz, W Gerhard.   

Abstract

We have examined how many different H chain variable (VH) and kappa-chain variable (Vk) germ-line genes are used in the antibody response to the influenza virus A/PR/8/34 hemagglutinin (PR8 HA), and have assessed how the expression of individual VH and/or Vk genes contributes to the generation of specificity for the HA. A panel of 51 hybridoma antibodies that recognize two antigenic regions on the HA were compared for the sequence of their Ig H and L chain V regions. The hybridomas were obtained from 28 individual BALB/c mice that had been immunized with PR8 under a variety of primary and secondary response immunization protocols. The degree and pattern of sequence similarity suggests that 29 different VH genes drawn from seven different VH gene families, and 25 different Vk genes drawn from 12 different Vk gene families were used in this panel. Based on current estimates of the total numbers of VH and Vk genes in the mouse, this suggests that between 2.5 and 10% of the entire VH and Vk germ-line repertoires were used by these hybridomas. Despite this extensive diversity, some V genes were repetitively identified among these hybridomas, and were most often expressed in the context of specific VH/Vk combinations. Because antibodies that used identical VH/Vk combinations also usually displayed similar reactivity patterns with a panel of mutant viruses, this indicates that VH/Vk pairing can be important in establishing the specificity of antibodies for the HA.

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Year:  1991        PMID: 1908881

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


  21 in total

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

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4.  Diversity of the murine antibody response targeting influenza A(H1N1pdm09) hemagglutinin.

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Journal:  Virology       Date:  2014-05-10       Impact factor: 3.616

5.  Fitness costs limit influenza A virus hemagglutinin glycosylation as an immune evasion strategy.

Authors:  Suman R Das; Scott E Hensley; Alexandre David; Loren Schmidt; James S Gibbs; Pere Puigbò; William L Ince; Jack R Bennink; Jonathan W Yewdell
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-21       Impact factor: 11.205

6.  DST4: a new, and probably the last, functional DH gene in the BALB/c mouse.

Authors:  A J Feeney; R Riblet
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7.  Clonal analysis of a human antibody response. II. Sequences of the VH genes of human IgM, IgG, and IgA to rabies virus reveal preferential utilization of VHIII segments and somatic hypermutation.

Authors:  H Ikematsu; N Harindranath; Y Ueki; A L Notkins; P Casali
Journal:  J Immunol       Date:  1993-02-15       Impact factor: 5.422

Review 8.  Immune recognition of influenza hemagglutinin as a viral and a neo-self-antigen.

Authors:  A J Caton; D M Cerasoli; F F Shih
Journal:  Immunol Res       Date:  1998       Impact factor: 2.829

9.  Selection of a single amino acid substitution in the hemagglutinin molecule by chicken eggs can render influenza A virus (H3) candidate vaccine ineffective.

Authors:  S Kodihalli; D M Justewicz; L V Gubareva; R G Webster
Journal:  J Virol       Date:  1995-08       Impact factor: 5.103

Review 10.  Developments in the scientific understanding of rheumatoid arthritis.

Authors:  Jörg J Goronzy; Cornelia M Weyand
Journal:  Arthritis Res Ther       Date:  2009-10-14       Impact factor: 5.156

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