Strategies to target long-lived plasma cells for treating hemophilia A inhibitors

Chao Lien Liu, Meghan J. Lyle, Simon C. Shin, Carol H. Miao

研究成果: 雜誌貢獻文章

6 引文 斯高帕斯(Scopus)

摘要

Long-lived plasma cells (LLPCs) can persistently produce anti-factor VIII (FVIII) antibodies which disrupt therapeutic effect of FVIII in hemophilia A patients with inhibitors. The migration of plasma cells to BM where they become LLPCs is largely controlled by an interaction between the chemokine ligand CXCL12 and its receptor CXCR4. AMD3100 combined with G-CSF inhibit their interactions, thus facilitating the mobilization of CD34+ cells and blocking the homing of LLPCs. These reagents were combined with anti-CD20 to reduce B-cells and the specific IL-2/IL-2mAb (JES6-1) complexes to induce Treg expansion for targeting anti-FVIII immune responses. Groups of mice primed with FVIII plasmid and protein respectively were treated with the combined regimen for six weeks, and a significant reduction of anti-FVIII inhibitor titers was observed, associated with the dramatic decrease of circulating and bone marrow CXCR4+ plasma cells. The combination regimens are highly promising in modulating pre-existing anti-FVIII antibodies in FVIII primed subjects.
原文英語
頁(從 - 到)65-73
頁數9
期刊Cellular Immunology
301
DOIs
出版狀態已發佈 - 三月 1 2016

ASJC Scopus subject areas

  • Immunology

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