333 related articles for article (PubMed ID: 20505144)
1. Augmented antibody response with premature germinal center regression in CD40L transgenic mice.
Kishi Y; Aiba Y; Higuchi T; Furukawa K; Tokuhisa T; Takemori T; Tsubata T
J Immunol; 2010 Jul; 185(1):211-9. PubMed ID: 20505144
[TBL] [Abstract][Full Text] [Related]
2. Constitutive CD40L expression on B cells prematurely terminates germinal center response and leads to augmented plasma cell production in T cell areas.
Bolduc A; Long E; Stapler D; Cascalho M; Tsubata T; Koni PA; Shimoda M
J Immunol; 2010 Jul; 185(1):220-30. PubMed ID: 20505142
[TBL] [Abstract][Full Text] [Related]
3. Antigen affinity controls rapid T-dependent antibody production by driving the expansion rather than the differentiation or extrafollicular migration of early plasmablasts.
Chan TD; Gatto D; Wood K; Camidge T; Basten A; Brink R
J Immunol; 2009 Sep; 183(5):3139-49. PubMed ID: 19666691
[TBL] [Abstract][Full Text] [Related]
4. IL-21 receptor is critical for the development of memory B cell responses.
Rankin AL; MacLeod H; Keegan S; Andreyeva T; Lowe L; Bloom L; Collins M; Nickerson-Nutter C; Young D; Guay H
J Immunol; 2011 Jan; 186(2):667-74. PubMed ID: 21169545
[TBL] [Abstract][Full Text] [Related]
5. Environmental and T cell-intrinsic factors limit the expansion of neonatal follicular T helper cells but may be circumvented by specific adjuvants.
Mastelic B; Kamath AT; Fontannaz P; Tougne C; Rochat AF; Belnoue E; Combescure C; Auderset F; Lambert PH; Tacchini-Cottier F; Siegrist CA
J Immunol; 2012 Dec; 189(12):5764-72. PubMed ID: 23162125
[TBL] [Abstract][Full Text] [Related]
6. Abrogation of pathogenic IgG autoantibody production in CD40L gene-deleted lupus-prone New Zealand Black mice.
Pau E; Chang NH; Loh C; Lajoie G; Wither JE
Clin Immunol; 2011 May; 139(2):215-27. PubMed ID: 21414847
[TBL] [Abstract][Full Text] [Related]
7. Expression of cellular FLIP by B cells is required for their participation in an immune response.
Coffey F; Manser T
J Immunol; 2010 May; 184(9):4871-9. PubMed ID: 20335528
[TBL] [Abstract][Full Text] [Related]
8. Cellular interaction in germinal centers. Roles of CD40 ligand and B7-2 in established germinal centers.
Han S; Hathcock K; Zheng B; Kepler TB; Hodes R; Kelsoe G
J Immunol; 1995 Jul; 155(2):556-67. PubMed ID: 7541819
[TBL] [Abstract][Full Text] [Related]
9. Early appearance of germinal center-derived memory B cells and plasma cells in blood after primary immunization.
Blink EJ; Light A; Kallies A; Nutt SL; Hodgkin PD; Tarlinton DM
J Exp Med; 2005 Feb; 201(4):545-54. PubMed ID: 15710653
[TBL] [Abstract][Full Text] [Related]
10. Cutting edge: IL-21 and TLR signaling regulate germinal center responses in a B cell-intrinsic manner.
Bessa J; Kopf M; Bachmann MF
J Immunol; 2010 May; 184(9):4615-9. PubMed ID: 20368279
[TBL] [Abstract][Full Text] [Related]
11. Cellular and molecular factors that regulate the differentiation and apoptosis of germinal center B cells. Anti-Ig down-regulates Fas expression of CD40 ligand-stimulated germinal center B cells and inhibits Fas-mediated apoptosis.
Choe J; Kim HS; Zhang X; Armitage RJ; Choi YS
J Immunol; 1996 Aug; 157(3):1006-16. PubMed ID: 8757604
[TBL] [Abstract][Full Text] [Related]
12. A role for lysosomal-associated protein transmembrane 5 in the negative regulation of surface B cell receptor levels and B cell activation.
Ouchida R; Kurosaki T; Wang JY
J Immunol; 2010 Jul; 185(1):294-301. PubMed ID: 20519653
[TBL] [Abstract][Full Text] [Related]
13. The xid mutation diminishes memory B cell generation but does not affect somatic hypermutation and selection.
Ridderstad A; Nossal GJ; Tarlinton DM
J Immunol; 1996 Oct; 157(8):3357-65. PubMed ID: 8871632
[TBL] [Abstract][Full Text] [Related]
14. B cell responses to a peptide epitope. VIII. Immune complex-mediated regulation of memory B cell generation within germinal centers.
Nayak BP; Agarwal A; Nakra P; Rao KV
J Immunol; 1999 Aug; 163(3):1371-81. PubMed ID: 10415037
[TBL] [Abstract][Full Text] [Related]
15. Lyn signaling to upregulate GANP is critical for the survival of high-affinity B cells in germinal centers of lymphoid organs.
Kuwahara K; Nakaya T; Phimsen S; Toda T; Kitabatake M; Kaji T; Takemori T; Watanabe T; Sakaguchi N
J Immunol; 2012 Oct; 189(7):3472-9. PubMed ID: 22942428
[TBL] [Abstract][Full Text] [Related]
16. Transgenic overexpression of G5PR that is normally augmented in centrocytes impairs the enrichment of high-affinity antigen-specific B cells, increases peritoneal B-1a cells, and induces autoimmunity in aged female mice.
Kitabatake M; Toda T; Kuwahara K; Igarashi H; Ohtsuji M; Tsurui H; Hirose S; Sakaguchi N
J Immunol; 2012 Aug; 189(3):1193-201. PubMed ID: 22753944
[TBL] [Abstract][Full Text] [Related]
17. Antigen drives very low affinity B cells to become plasmacytes and enter germinal centers.
Dal Porto JM; Haberman AM; Shlomchik MJ; Kelsoe G
J Immunol; 1998 Nov; 161(10):5373-81. PubMed ID: 9820511
[TBL] [Abstract][Full Text] [Related]
18. A soluble form of IL-13 receptor alpha 1 promotes IgG2a and IgG2b production by murine germinal center B cells.
Poudrier J; Graber P; Herren S; Gretener D; Elson G; Berney C; Gauchat JF; Kosco-Vilbois MH
J Immunol; 1999 Aug; 163(3):1153-61. PubMed ID: 10415009
[TBL] [Abstract][Full Text] [Related]
19. BASH-deficient mice: limited primary repertoire and antibody formation, but sufficient affinity maturation and memory B cell generation, in anti-NP response.
Yamamoto M; Nojima T; Hayashi K; Goitsuka R; Furukawa K; Azuma T; Kitamura D
Int Immunol; 2004 Aug; 16(8):1161-71. PubMed ID: 15237108
[TBL] [Abstract][Full Text] [Related]
20. The pleckstrin homology domain adaptor protein Bam32/DAPP1 is required for germinal center progression.
Zhang TT; Al-Alwan M; Marshall AJ
J Immunol; 2010 Jan; 184(1):164-72. PubMed ID: 19949096
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
