Literature DB >> 1086236

Antibody response to phosphorylcholine in vitro. I. Studies on the frequency of precursor cells, average clone size and cellular cooperation.

H Cosenza, J Quintáns, I Lefkovits.   

Abstract

The anti-phosphorylcholine (PC) antibodies synthesized by BALB/c spleen cells in microcultures upon immunization with heat-killed vaccine of Pneumococci R36A (Pn) are directed exclusively to the PC epitope. These antibodies are of very restricted avidity and 88% of the responding clones express the idiotype characteristic of the TEPC-15 PC-binding myeloma. This idiotypic restriction appears to be due to the absence of clones capable of expressing other idiotypes, rather than to "clonal dominance". The estimated frequency of precursor cells for the PC epitope is 1 X 10(-5) to 2.5 X 10(-5). These precursors give rise to clones with an average size of 9 plaque-forming cells. When the logarithm of the number of negative wells was plotted against the number of spleen cells/well, the fraction of nonresponding cultures decreased exponentially as the number of spleen cells was increased. This indicated that only one cell type was limiting in our assay, presumably a B cell. Furthermore, treatment of spleen cells with AKR anti serum completely abolished the response to sheep red cells without affecting the response to PC. It is concluded that PC is a T cell-independent antigen. Of interest was the finding that PC requires adherent (A) cells and this is a particular characteristic of PC, since most T cell-independent antigens have been found not to require A cells. Reasons for the possible homogeneity of the response to PC are also discussed.

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Year:  1975        PMID: 1086236     DOI: 10.1002/eji.1830050510

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  9 in total

1.  In vivo polyclonal stimulation of antibody secretion by two types of bacteria.

Authors:  D Levitt; M A Bach
Journal:  Immunology       Date:  1985-08       Impact factor: 7.397

2.  Clonal dominance: loss and restoration in adoptive transfer.

Authors:  D R Kaplan; J Quintans; H Köhler
Journal:  Proc Natl Acad Sci U S A       Date:  1978-04       Impact factor: 11.205

3.  Enhancing antibody: a novel component of the immune response.

Authors:  D A Nemazee; V L Sato
Journal:  Proc Natl Acad Sci U S A       Date:  1982-06       Impact factor: 11.205

4.  Primary in vitro plaque-forming cell response to DAGG-Ficoll: LPS-induced enhancement mediated by interleukin-1.

Authors:  J L Curtis; A A Nordin
Journal:  Immunology       Date:  1984-08       Impact factor: 7.397

5.  Interactions of C-reactive protein with the complement system. III. Complement-dependent passive hemolysis initiated by CRP.

Authors: 
Journal:  J Exp Med       Date:  1975-11-01       Impact factor: 14.307

6.  Idiotype connectance in the immune system. II. A heavy chain variable region idiotope that dominates the antibody response to the p-azobenzenearsonate group is a minor idiotope in the response to trinitrophenyl group.

Authors:  P V Hornbeck; G K Lewis
Journal:  J Exp Med       Date:  1985-01-01       Impact factor: 14.307

7.  The B cell repertoire revealed by major histocompatibility complex-specific helper T cells. I. Frequencies of a genetically defined V region marker among mitogen- and T helper cell-reactive B lymphocytes in normal and immunized mice.

Authors:  D Primi; P A Cazenave
Journal:  J Exp Med       Date:  1984-04-01       Impact factor: 14.307

8.  Expression of phosphorylcholine-specific B cells during murine development.

Authors:  N H Sigal; A R Pickard; E S Metcalf; P J Gearhart; N R Klinman
Journal:  J Exp Med       Date:  1977-10-01       Impact factor: 14.307

9.  Cross-reactivity between C-reactive protein and idiotypic determinants on A phosphocholine-binding murine myeloma protein.

Authors:  J E Volanakis; J F Kearney
Journal:  J Exp Med       Date:  1981-06-01       Impact factor: 14.307

  9 in total

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