216 related articles for article (PubMed ID: 14718515)
1. Aiolos is required for the generation of high affinity bone marrow plasma cells responsible for long-term immunity.
Cortés M; Georgopoulos K
J Exp Med; 2004 Jan; 199(2):209-19. PubMed ID: 14718515
[TBL] [Abstract][Full Text] [Related]
2. Lack of the transcriptional coactivator OBF-1 prevents the development of systemic lupus erythematosus-like phenotypes in Aiolos mutant mice.
Sun J; Matthias G; Mihatsch MJ; Georgopoulos K; Matthias P
J Immunol; 2003 Feb; 170(4):1699-706. PubMed ID: 12574333
[TBL] [Abstract][Full Text] [Related]
3. Lasting antibody responses are mediated by a combination of newly formed and established bone marrow plasma cells drawn from clonally distinct precursors.
Chernova I; Jones DD; Wilmore JR; Bortnick A; Yucel M; Hershberg U; Allman D
J Immunol; 2014 Nov; 193(10):4971-9. PubMed ID: 25326027
[TBL] [Abstract][Full Text] [Related]
4. Low-affinity IgM antibodies lacking somatic hypermutations are produced in the secondary response of C57BL/6 mice to (4-hydroxy-3-nitrophenyl)acetyl hapten.
Murakami A; Moriyama H; Osako-Kabasawa M; Endo K; Nishimura M; Udaka K; Muramatsu M; Honjo T; Azuma T; Shimizu T
Int Immunol; 2014 Apr; 26(4):195-208. PubMed ID: 24285827
[TBL] [Abstract][Full Text] [Related]
5. Aiolos regulates B cell activation and maturation to effector state.
Wang JH; Avitahl N; Cariappa A; Friedrich C; Ikeda T; Renold A; Andrikopoulos K; Liang L; Pillai S; Morgan BA; Georgopoulos K
Immunity; 1998 Oct; 9(4):543-53. PubMed ID: 9806640
[TBL] [Abstract][Full Text] [Related]
6. Protective long-term antibody memory by antigen-driven and T help-dependent differentiation of long-lived memory B cells to short-lived plasma cells independent of secondary lymphoid organs.
Ochsenbein AF; Pinschewer DD; Sierro S; Horvath E; Hengartner H; Zinkernagel RM
Proc Natl Acad Sci U S A; 2000 Nov; 97(24):13263-8. PubMed ID: 11069289
[TBL] [Abstract][Full Text] [Related]
7. Sustained antibody responses depend on CD28 function in bone marrow-resident plasma cells.
Rozanski CH; Arens R; Carlson LM; Nair J; Boise LH; Chanan-Khan AA; Schoenberger SP; Lee KP
J Exp Med; 2011 Jul; 208(7):1435-46. PubMed ID: 21690252
[TBL] [Abstract][Full Text] [Related]
8. Survival of long-lived plasma cells is independent of antigen.
Manz RA; Löhning M; Cassese G; Thiel A; Radbruch A
Int Immunol; 1998 Nov; 10(11):1703-11. PubMed ID: 9846699
[TBL] [Abstract][Full Text] [Related]
9. Swiprosin-1/EFhd2 limits germinal center responses and humoral type 2 immunity.
Brachs S; Turqueti-Neves A; Stein M; Reimer D; Brachvogel B; Bösl M; Winkler T; Voehringer D; Jäck HM; Mielenz D
Eur J Immunol; 2014 Nov; 44(11):3206-19. PubMed ID: 25092375
[TBL] [Abstract][Full Text] [Related]
10. Short-lived and long-lived bone marrow plasma cells are derived from a novel precursor population.
O'Connor BP; Cascalho M; Noelle RJ
J Exp Med; 2002 Mar; 195(6):737-45. PubMed ID: 11901199
[TBL] [Abstract][Full Text] [Related]
11. Plasma cell numbers decrease in bone marrow of old patients.
Pritz T; Lair J; Ban M; Keller M; Weinberger B; Krismer M; Grubeck-Loebenstein B
Eur J Immunol; 2015 Mar; 45(3):738-46. PubMed ID: 25430805
[TBL] [Abstract][Full Text] [Related]
12. Immunization induces activation of bone marrow eosinophils required for plasma cell survival.
Chu VT; Berek C
Eur J Immunol; 2012 Jan; 42(1):130-7. PubMed ID: 22057654
[TBL] [Abstract][Full Text] [Related]
13. Antigen-selected, immunoglobulin-secreting cells persist in human spleen and bone marrow.
Ellyard JI; Avery DT; Phan TG; Hare NJ; Hodgkin PD; Tangye SG
Blood; 2004 May; 103(10):3805-12. PubMed ID: 14701691
[TBL] [Abstract][Full Text] [Related]
14. Enhanced differentiation of splenic plasma cells but diminished long-lived high-affinity bone marrow plasma cells in aged mice.
Han S; Yang K; Ozen Z; Peng W; Marinova E; Kelsoe G; Zheng B
J Immunol; 2003 Feb; 170(3):1267-73. PubMed ID: 12538685
[TBL] [Abstract][Full Text] [Related]
15. Long-lived plasma cells are generated in mucosal immune responses and contribute to the bone marrow plasma cell pool in mice.
Lemke A; Kraft M; Roth K; Riedel R; Lammerding D; Hauser AE
Mucosal Immunol; 2016 Jan; 9(1):83-97. PubMed ID: 25943272
[TBL] [Abstract][Full Text] [Related]
16. FcgammaRIIb controls bone marrow plasma cell persistence and apoptosis.
Xiang Z; Cutler AJ; Brownlie RJ; Fairfax K; Lawlor KE; Severinson E; Walker EU; Manz RA; Tarlinton DM; Smith KG
Nat Immunol; 2007 Apr; 8(4):419-29. PubMed ID: 17322888
[TBL] [Abstract][Full Text] [Related]
17. No strict requirement for eosinophils for bone marrow plasma cell survival.
Bortnick A; Chernova I; Spencer SP; Allman D
Eur J Immunol; 2018 May; 48(5):815-821. PubMed ID: 29442367
[TBL] [Abstract][Full Text] [Related]
18. 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]
19.
Männe C; Takaya A; Yamasaki Y; Mursell M; Hojyo S; Wu TY; Sarkander J; McGrath MA; Cornelis R; Hahne S; Cheng Q; Kawamoto T; Hiepe F; Kaufmann SHE; Yamamoto T; Radbruch A; Tokoyoda K
Proc Natl Acad Sci U S A; 2019 Apr; 116(15):7425-7430. PubMed ID: 30910977
[TBL] [Abstract][Full Text] [Related]
20. Environmental sensing by mature B cells is controlled by the transcription factors PU.1 and SpiB.
Willis SN; Tellier J; Liao Y; Trezise S; Light A; O'Donnell K; Garrett-Sinha LA; Shi W; Tarlinton DM; Nutt SL
Nat Commun; 2017 Nov; 8(1):1426. PubMed ID: 29127283
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
