Literature DB >> 2492056

Structural characterization of antiidiotypic antibodies. Evidence that Ab2s are derived from the germline differently than Ab1s.

K Meek1, C Hasemann, B Pollok, S S Alkan, M Brait, M Slaoui, J Urbain, J D Capra.   

Abstract

We have found that syngeneic Ab2s in the antiarsonate system are serologically and structurally similar to one another. In contrast, the allogeneic Ab2 response is heterogeneous and derives from a large number of unrelated germline gene segments. The Ab2 response of the BALB/c strain to polyclonal A/J Ars A molecules can probably best be compared with a response to a foreign protein and might have been predicted in a strain that completely lacks the H chain V region gene from which the Ab1 derives. Partial variable region sequences of Ab2s from three other systems in addition to previously reported Ab2 structures indicates that this difference in allogeneic vs. syngeneic Ab2s may be a general phenomena. These data support Jerne's hypothesis of complementary V region genes existing in the germline. However, there is good evidence that these antiidiotypic antibodies are not derived directly from the germline, as somatic processes most likely play an important role in their generation. The D segments of Ab2s in the arsonate system as well as in other systems, are novel in structure and cannot easily be explained by previously described germline D segments. D-D fusion may play a role in the generation of the third hypervariable region in these antibodies.

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Year:  1989        PMID: 2492056      PMCID: PMC2189219          DOI: 10.1084/jem.169.2.519

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  40 in total

1.  V kappa and J kappa gene segments of A/J Ars-A antibodies: somatic recombination generates the essential arginine at the junction of the variable and joining regions.

Authors:  I Sanz; J D Capra
Journal:  Proc Natl Acad Sci U S A       Date:  1987-02       Impact factor: 11.205

2.  Site-directed mutagenesis of an invariant amino acid residue at the variable-diversity segments junction of an antibody.

Authors:  J Sharon; M L Gefter; T Manser; M Ptashne
Journal:  Proc Natl Acad Sci U S A       Date:  1986-04       Impact factor: 11.205

3.  A rapid method for cloning and sequencing variable-region genes of expressed immunoglobulins.

Authors:  S Levy; E Mendel; S Kon
Journal:  Gene       Date:  1987       Impact factor: 3.688

4.  A single VH-gene associated with a variety of D- and J-segments encodes for a large family of ABPC48-related antibodies induced by antiidiotypic immunization.

Authors:  P Legrain; J Rocca-Serra; A Moulin; M Fougereau; G Buttin
Journal:  Mol Immunol       Date:  1985-04       Impact factor: 4.407

5.  Structural basis of stimulatory anti-idiotypic antibodies.

Authors:  H L Cheng; A K Sood; R E Ward; T Kieber-Emmons; H Kohler
Journal:  Mol Immunol       Date:  1988-01       Impact factor: 4.407

6.  VH families in the antibody response to p-azophenylarsonate: correlation between serology and amino acid sequence.

Authors:  E C Milner; J D Capra
Journal:  J Immunol       Date:  1982-07       Impact factor: 5.422

7.  Towards a network theory of the immune system.

Authors:  N K Jerne
Journal:  Ann Immunol (Paris)       Date:  1974-01

8.  Structural and serological analysis of cross-reactive idiotypes: comparison of heavy and light chain families of anti-arsonate antibodies.

Authors:  S S Alkan
Journal:  Ann Immunol (Paris)       Date:  1984 Jan-Feb

9.  Classification of mouse VK groups based on the partial amino acid sequence to the first invariant tryptophan: impact of 14 new sequences from IgG myeloma proteins.

Authors:  M Potter; J B Newell; S Rudikoff; E Haber
Journal:  Mol Immunol       Date:  1982-12       Impact factor: 4.407

10.  Monoclonal vs. heterogeneous anti-H-8 antibodies in the analysis of the anti-phosphorylcholine response in BALB/c mice.

Authors:  J F Kearney; R Barletta; Z S Quan; J Quintáns
Journal:  Eur J Immunol       Date:  1981-11       Impact factor: 5.532

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  6 in total

1.  Molecular characterization of monoclonal CRIA-positive anti-arsonate antibodies derived from idiotype-negative mice bearing a light chain polymorphism.

Authors:  J Tassignon; M Brait; J Ismaili; J Urbain; P Gottlieb; A Brown; C A Hasemann; J D Capra; K Meek
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

2.  Sequence homologies, N sequence insertion and JH gene utilization in VHDJH joining: implications for the joining mechanism and the ontogenetic timing of Ly1 B cell and B-CLL progenitor generation.

Authors:  H Gu; I Förster; K Rajewsky
Journal:  EMBO J       Date:  1990-07       Impact factor: 11.598

3.  Anti-DNA antibodies from autoimmune mice arise by clonal expansion and somatic mutation.

Authors:  M Shlomchik; M Mascelli; H Shan; M Z Radic; D Pisetsky; A Marshak-Rothstein; M Weigert
Journal:  J Exp Med       Date:  1990-01-01       Impact factor: 14.307

4.  Novel rearrangements at the immunoglobulin D locus. Inversions and fusions add to IgH somatic diversity.

Authors:  K D Meek; C A Hasemann; J D Capra
Journal:  J Exp Med       Date:  1989-07-01       Impact factor: 14.307

5.  Lack of N regions in fetal and neonatal mouse immunoglobulin V-D-J junctional sequences.

Authors:  A J Feeney
Journal:  J Exp Med       Date:  1990-11-01       Impact factor: 14.307

6.  Both IgM and IgG anti-DNA antibodies are the products of clonally selective B cell stimulation in (NZB x NZW)F1 mice.

Authors:  D M Tillman; N T Jou; R J Hill; T N Marion
Journal:  J Exp Med       Date:  1992-09-01       Impact factor: 14.307

  6 in total

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