Literature DB >> 6605381

Relationship of germinal centers in lymphoid tissue to immunologic memory. VI. Transfer of B cell memory with lymph node cells fractionated according to their receptors for peanut agglutinin.

R F Coico, B S Bhogal, G J Thorbecke.   

Abstract

We isolated germinal center B cells by exploiting their high affinity for peanut agglutinin (PNA). The PNA+ and PNA- B cells, fractionated by panning on PNA-coated petri dishes, were examined for their ability to transfer memory responses to irradiated recipients at various times after priming. With such fractionated B cells from lymph nodes taken at the peak of germinal center formation, the largest response was obtained in recipients of the PNA+ B cell population. At 4 to 5 wk after priming, and 10 days after challenge with an unrelated antigen, memory responses were approximately equal in recipients of PNA+ or PNA- B cells. At 14 wk after priming, memory responses were found only in recipients of the PNA- B cell population. Memory B cells from the spleen, taken from mice primed in the footpad 8 wk earlier, were also PNA-. Finally, we show that boosting with a TNP-conjugate in the footpad, 6 mo after priming in the same footpad, induced the reappearance of marked memory responsiveness in the PNA+ B cell fraction of the draining node.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6605381

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


  58 in total

Review 1.  B-cell memory and the persistence of antibody responses.

Authors:  I C MacLennan; C García de Vinuesa; M Casamayor-Palleja
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-03-29       Impact factor: 6.237

Review 2.  Relative roles of somatic and Darwinian evolution in shaping the antibody response.

Authors:  M Diaz; N R Klinman
Journal:  Immunol Res       Date:  2000       Impact factor: 2.829

3.  Regulation of VH gene repertoire and somatic mutation in germinal centre B cells by passively administered antibody.

Authors:  H Song; X Nie; S Basu; M Singh; J Cerny
Journal:  Immunology       Date:  1999-10       Impact factor: 7.397

4.  B cell immunopoiesis: visualizing the impact of CD40 engagement on the course of T cell-independent immune responses in an Ig transgenic system.

Authors:  L D Erickson; L A Vogel; M Cascalho; J Wong; M Wabl; B G Durell; R J Noelle
Journal:  Eur J Immunol       Date:  2000-11       Impact factor: 5.532

5.  Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice.

Authors:  M B Alimzhanov; D V Kuprash; M H Kosco-Vilbois; A Luz; R L Turetskaya; A Tarakhovsky; K Rajewsky; S A Nedospasov; K Pfeffer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

6.  Responses of single germinal-center B cells in T-cell-dependent microculture.

Authors:  A George; J J Cebra
Journal:  Proc Natl Acad Sci U S A       Date:  1991-01-01       Impact factor: 11.205

7.  Iccosomes and the secondary antibody response.

Authors:  G F Burton; M H Kosco; A K Szakal; J G Tew
Journal:  Immunology       Date:  1991-07       Impact factor: 7.397

8.  T lymphocytes in rat germinal centres belong to an ER3+ subpopulation of CD4+ cells.

Authors:  R H Vonderheide; S V Hunt
Journal:  Immunology       Date:  1990-04       Impact factor: 7.397

9.  Does the availability of either B cells or CD4+ cells limit germinal centre formation?

Authors:  R H Vonderheide; S V Hunt
Journal:  Immunology       Date:  1990-03       Impact factor: 7.397

10.  Antibody to the ligand for CD40 (gp39) inhibits murine AIDS-associated splenomegaly, hypergammaglobulinemia, and immunodeficiency in disease-susceptible C57BL/6 mice.

Authors:  K A Green; K M Crassi; J D Laman; A Schoneveld; R R Strawbridge; T M Foy; R J Noelle; W R Green
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.