Literature DB >> 389782

The influence of T cells on the initiation and expression of immunological memory.

D W Dresser, A M Popham.   

Abstract

Nude and normal CBA mice have been used in adoptive transfer experiments to analyse the development of immunological memory. The development of B-cell memory to xenogeneic erythrocyte antigens is to a very large degree dependent on the presence of T cells, with IgG memory being somewhat more dependent than IgM memory. In this system, the expression of B memory, that is the transformation of memory cells to antibody-secreting cells under the inductive influence of antigen, is largely dependent on the presence of T cells. Primed (educated) T cells can have an antigen-specific potentiating effect on unprimed B cells in the presence of antigen.

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Year:  1979        PMID: 389782      PMCID: PMC1457934     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  25 in total

1.  A study of the adoptive secondary response to a protein antigen in mice.

Authors:  D W DRESSER
Journal:  Proc R Soc Lond B Biol Sci       Date:  1961-07-25

2.  Secondary IgG responses to type 3 pneumococcal polysaccharide. III. T cell requirement for development of B memory cells.

Authors:  H Braley-Mullen
Journal:  Eur J Immunol       Date:  1977-11       Impact factor: 5.532

3.  An analysis of B cell memory. I. Interaction of helper and suppressor effects in the in vitro expression of IgM memory.

Authors:  L M Pilarski
Journal:  Cell Immunol       Date:  1978-10       Impact factor: 4.868

4.  Clonal expansion of IgM B memory cells in vitro.

Authors:  L M Pilarski
Journal:  Cell Immunol       Date:  1978-10       Impact factor: 4.868

5.  Specific suppression of immune responses.

Authors:  D A Rowley; F W Fitch; F P Stuart; H Köhler; H Cosenza
Journal:  Science       Date:  1973-09-21       Impact factor: 47.728

Review 6.  Cellular cooperation in the antibody response of mice to two serum albumins: specific function of thymus cells.

Authors:  R B Taylor
Journal:  Transplant Rev       Date:  1969

7.  Expression of IgG memory response in vitro to thymus-dependent and thymus-independent antigens.

Authors:  T V Tittle; M B Rittenberg
Journal:  Cell Immunol       Date:  1978-01       Impact factor: 4.868

8.  Role of membrane receptors in the induction of an in vitro secondary anti-hapten response. II. Antigen-immunoglobulin receptor interaction is not required for B memory cell proliferation.

Authors:  S Cammisuli; C Henry
Journal:  Eur J Immunol       Date:  1978-09       Impact factor: 5.532

9.  Role of membrane receptors in the induction of an in vitro secondary anti-hapten response. I. differentiation of B memory cells to plasma cells is independent of antigen-immunoglobulin receptor interaction.

Authors:  S Cammisuli; C Henry; L Wofsy
Journal:  Eur J Immunol       Date:  1978-09       Impact factor: 5.532

10.  Transition in the character of immunological memory in mice after immunization. II. Memory in T and B cell populations.

Authors:  M Takaoki
Journal:  Jpn J Microbiol       Date:  1976-12
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  11 in total

1.  Immunological memory and lymphoblast-migration in mice infected with Hymenolepis nana.

Authors:  C Palmas; G Bortoletti; M Conchedda; F Gabriele
Journal:  Z Parasitenkd       Date:  1986

2.  Cyclic development of immunological memory to bacterial lipopolysaccharide.

Authors:  P J Baker; J R Hiernaux; P W Stashak; J A Rudbach
Journal:  Infect Immun       Date:  1985-04       Impact factor: 3.441

3.  Role of T cells in the development of memory B cells. Quantitative and qualitative analysis.

Authors:  D E Lafrenz; T L Feldbush
Journal:  Immunology       Date:  1981-09       Impact factor: 7.397

Review 4.  How many T cells help one B cell?

Authors:  H Waldmann; J Phillips
Journal:  Springer Semin Immunopathol       Date:  1980-05

5.  Antigen requirements for priming of IgG producing B memory cells specific for Type III pneumococcal polysaccharide.

Authors:  H Braley-Mullen
Journal:  Immunology       Date:  1980-08       Impact factor: 7.397

6.  Immunoglobulin M and G antibody responses and persistence of these antibodies in adults after vaccination with a combined meningococcal group A and group C polysaccharide vaccine.

Authors:  E C Beuvery; A B Leussink; R W Van Delft; R H Tiesjema; J Nagel
Journal:  Infect Immun       Date:  1982-08       Impact factor: 3.441

7.  Activation of human B lymphocytes after immunization with pneumococcal polysaccharides.

Authors:  J H Kehrl; A S Fauci
Journal:  J Clin Invest       Date:  1983-04       Impact factor: 14.808

8.  Differences in putative minor histocompatibility but not IgH genes can prevent T-cell priming and T--B co-operation in the response of mice to sheep erythrocytes.

Authors:  D W Dresser; A M Popham; R Hunt
Journal:  Immunology       Date:  1982-07       Impact factor: 7.397

9.  Enterobacterial common antigen-tetanus toxoid conjugate as immunogen.

Authors:  C Lugowski; M Kułakowska; E Romanowska
Journal:  Infect Immun       Date:  1983-12       Impact factor: 3.441

10.  Comparison of the induction of immunoglobulin M and G antibodies in mice with purified pneumococcal type 3 and meningococcal group C polysaccharides and their protein conjugates.

Authors:  E C Beuvery; F van Rossum; J Nagel
Journal:  Infect Immun       Date:  1982-07       Impact factor: 3.441

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