Literature DB >> 30656359

Llama peripheral B-cell populations producing conventional and heavy chain-only IgG subtypes are phenotypically indistinguishable but immunogenetically distinct.

Kevin A Henry1, Henk van Faassen2, Doreen Harcus3, Anne Marcil3, Jennifer J Hill2, Serge Muyldermans4, C Roger MacKenzie2,5.   

Abstract

Camelid ungulates produce homodimeric heavy chain-only antibodies (HCAbs) in addition to conventional antibodies consisting of paired heavy and light chains. In the llama, HCAbs are made up by at least two subclasses (long-hinge IgG2b and short-hinge IgG2c HCAbs vs. conventional heterotetrameric IgG1s). Here, we generated murine monoclonal antibodies (mAbs) specific for the hinge-CH2 boundary of llama IgG2b (mAb 1C10) and the Fc of llama IgG2c HCAbs (mAb 5E4). Flow cytometric analysis of llama peripheral blood lymphocytes revealed that IgG1+, IgG2b+ and IgG2c+ B cells could be distinguished using mAbs 1C10/5E4 but had equivalent expression of three other cell-surface markers. MiSeq sequencing of the peripheral B cell repertoires of three llamas showed that (i) IgG2b and IgG2c HCAbs were present in similar proportions in the repertoire, (ii) a subset of IgG2b and IgG2c HCAbs, but not IgG1s, entirely lacked a hinge exon and showed direct VHH-CH2 splicing; these "hingeless" HCAbs were clonally expanded, somatically mutated and derived from hinged HCAb precursors, (iii) substantial repertoire overlap existed between IgG subclasses, especially between IgG2b and IgG2c HCAbs, (iv) the complementarity-determining region (CDR)-H3 length distributions of IgG2b and IgG2c HCAbs were broader and biased towards longer lengths compared with IgG1s due to increased N-nucleotide addition, (v) IgG2b and IgG2c HCAbs used a more restricted set of IGHV genes compared with IgG1s, and (vi) IgG2b and IgG2c HCAbs had elevated somatic mutations rates of both CDRs and framework regions (FRs) compared with IgG1s, especially of CDR-H1 and FR3. The distinct molecular features of llama IgG1, IgG2b and IgG2c antibodies imply that these subclasses may have divergent immunological functions and suggest that specific mechanisms operate to diversify HCAb repertoires in the absence of a light chain.

Entities:  

Keywords:  Heavy chain-only antibody; Immunogenetics; Llama; Next-generation DNA sequencing; Single-domain antibody; VHH

Mesh:

Substances:

Year:  2019        PMID: 30656359     DOI: 10.1007/s00251-018-01102-9

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


  45 in total

1.  Application of monoclonal antibodies in functional and comparative investigations of heavy-chain immunoglobulins in new world camelids.

Authors:  L P Daley; L F Gagliardo; M S Duffy; M C Smith; J A Appleton
Journal:  Clin Diagn Lab Immunol       Date:  2005-03

2.  Comparison of llama VH sequences from conventional and heavy chain antibodies.

Authors:  K B Vu; M A Ghahroudi; L Wyns; S Muyldermans
Journal:  Mol Immunol       Date:  1997 Nov-Dec       Impact factor: 4.407

3.  Isolation of TGF-β-neutralizing single-domain antibodies of predetermined epitope specificity using next-generation DNA sequencing.

Authors:  Kevin A Henry; Greg Hussack; Cathy Collins; John C Zwaagstra; Jamshid Tanha; C Roger MacKenzie
Journal:  Protein Eng Des Sel       Date:  2016-09-08       Impact factor: 1.650

4.  Distinct patterns of IgH structure and organization in a divergent lineage of chrondrichthyan fishes.

Authors:  J P Rast; C T Amemiya; R T Litman; S J Strong; G W Litman
Journal:  Immunogenetics       Date:  1998       Impact factor: 2.846

5.  Loss of splice consensus signal is responsible for the removal of the entire C(H)1 domain of the functional camel IGG2A heavy-chain antibodies.

Authors:  V K Nguyen; R Hamers; L Wyns; S Muyldermans
Journal:  Mol Immunol       Date:  1999-06       Impact factor: 4.407

6.  Camelid Ig V genes reveal significant human homology not seen in therapeutic target genes, providing for a powerful therapeutic antibody platform.

Authors:  Alex Klarenbeek; Khalil El Mazouari; Aline Desmyter; Christophe Blanchetot; Anna Hultberg; Natalie de Jonge; Rob C Roovers; Christian Cambillau; Sylvia Spinelli; Jurgen Del-Favero; Theo Verrips; Hans J de Haard; Ikbel Achour
Journal:  MAbs       Date:  2015       Impact factor: 5.857

Review 7.  Emergence and evolution of functional heavy-chain antibodies in Camelidae.

Authors:  K E Conrath; U Wernery; S Muyldermans; V K Nguyen
Journal:  Dev Comp Immunol       Date:  2003-02       Impact factor: 3.636

8.  Naturally occurring antibodies devoid of light chains.

Authors:  C Hamers-Casterman; T Atarhouch; S Muyldermans; G Robinson; C Hamers; E B Songa; N Bendahman; R Hamers
Journal:  Nature       Date:  1993-06-03       Impact factor: 49.962

9.  Human IgG2- and IgG4-expressing memory B cells display enhanced molecular and phenotypic signs of maturity and accumulate with age.

Authors:  Britt G de Jong; Hanna IJspeert; Lemelinda Marques; Mirjam van der Burg; Jacques Jm van Dongen; Bruno G Loos; Menno C van Zelm
Journal:  Immunol Cell Biol       Date:  2017-05-26       Impact factor: 5.126

Review 10.  Antigen recognition by single-domain antibodies: structural latitudes and constraints.

Authors:  Kevin A Henry; C Roger MacKenzie
Journal:  MAbs       Date:  2018-08-15       Impact factor: 5.857

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  5 in total

1.  Nanobodies: From Serendipitous Discovery of Heavy Chain-Only Antibodies in Camelids to a Wide Range of Useful Applications.

Authors:  Fangling Ji; Jun Ren; Cécile Vincke; Lingyun Jia; Serge Muyldermans
Journal:  Methods Mol Biol       Date:  2022

Review 2.  Camelid Single-Domain Antibodies: Promises and Challenges as Lifesaving Treatments.

Authors:  Mehdi Arbabi-Ghahroudi
Journal:  Int J Mol Sci       Date:  2022-04-30       Impact factor: 6.208

Review 3.  The Camel Adaptive Immune Receptors Repertoire as a Singular Example of Structural and Functional Genomics.

Authors:  Salvatrice Ciccarese; Pamela A Burger; Elena Ciani; Vito Castelli; Giovanna Linguiti; Martin Plasil; Serafina Massari; Petr Horin; Rachele Antonacci
Journal:  Front Genet       Date:  2019-10-17       Impact factor: 4.599

4.  Deiminated proteins in extracellular vesicles and serum of llama (Lama glama)-Novel insights into camelid immunity.

Authors:  Michael F Criscitiello; Igor Kraev; Sigrun Lange
Journal:  Mol Immunol       Date:  2019-11-13       Impact factor: 4.407

Review 5.  Extracellular Vesicles in Veterinary Medicine.

Authors:  Valentina Moccia; Alessandro Sammarco; Laura Cavicchioli; Massimo Castagnaro; Laura Bongiovanni; Valentina Zappulli
Journal:  Animals (Basel)       Date:  2022-10-10       Impact factor: 3.231

  5 in total

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