共 64 条
Rate of Immune Complex Cycling in Follicular Dendritic Cells Determines the Extent of Protecting Antigen Integrity and Availability to Germinal Center B Cells
被引:16
作者:

Arulraj, Theinmozhi
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机构:
Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany

Binder, Sebastian C.
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h-index: 0
机构:
Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany
Ctr Individualized Infect Med, D-30625 Hannover, Germany Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany

Meyer-Hermann, Michael
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h-index: 0
机构:
Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany
Ctr Individualized Infect Med, D-30625 Hannover, Germany
Braunschweig Univ Technol, Inst Biochem Biotechnol & Bioinformat, D-38106 Braunschweig, Germany Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany
机构:
[1] Braunschweig Integrated Ctr Syst Biol, Helmholtz Ctr Infect Res, Dept Syst Immunol, Rebenring 56, D-38106 Braunschweig, Germany
[2] Ctr Individualized Infect Med, D-30625 Hannover, Germany
[3] Braunschweig Univ Technol, Inst Biochem Biotechnol & Bioinformat, D-38106 Braunschweig, Germany
基金:
欧盟地平线“2020”;
关键词:
LYMPH-NODE;
DEPENDENT TRANSPORT;
AFFINITY MATURATION;
MOUSE SPLEEN;
RECEPTOR;
SELECTION;
ENDOCYTOSIS;
EXPRESSION;
RETENTION;
MAINTENANCE;
D O I:
10.4049/jimmunol.2001355
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
071005 [微生物学];
100108 [医学免疫学];
摘要:
Follicular dendritic cells (FDCs) retain immune complexes (ICs) for prolonged time periods and are important for germinal center (GC) reactions. ICs undergo periodic cycling in FDCs, a mechanism supporting an extended half-life of Ag. Based on experimental data, we estimated that the average residence time of PE-ICs on FDC surface and interior were 21 and 36 min, respectively. GC simulations show that Ag cycling might impact GC dynamics because of redistribution of Ag on the FDC surface and by protecting Ag from degradation. Ag protection and influence on GC dynamics varied with Ag cycling time and total Ag concentration. Simulations predict that blocking Ag cycling terminates the GC reaction and decreases plasma cell production. Considering that cycling of Ag could be a target for the modulation of GC reactions, our findings highlight the importance of understanding the mechanism and regulation of IC cycling in FDCs.
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页码:1436 / 1442
页数:7
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Australian Natl Univ, Ctr Personalised Immunol, John Curtin Sch Med Res, Canberra, ACT, Australia Australian Natl Univ, Dept Immunol & Infect Dis, John Curtin Sch Med Res, Canberra, ACT, Australia

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Doglioni, Claudio
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de St Groth, Barbara Fazekas
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Cook, Matthew C.
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Australian Natl Univ, Ctr Personalised Immunol, John Curtin Sch Med Res, Canberra, ACT, Australia
Canberra Hosp, Dept Immunol, Canberra, ACT, Australia Australian Natl Univ, Dept Immunol & Infect Dis, John Curtin Sch Med Res, Canberra, ACT, Australia

Vinuesa, Carola G.
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Australian Natl Univ, Ctr Personalised Immunol, John Curtin Sch Med Res, Canberra, ACT, Australia Australian Natl Univ, Dept Immunol & Infect Dis, John Curtin Sch Med Res, Canberra, ACT, Australia
