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Abstract Number: 1895

Marked Immune Cell Subset Changes in Refractory Lupus Patients in a Phase I Trial of Allogenic Mesenchymal Stem Cells

Caroline Wallace Fugle1, Chungwen Wei2, Ignacio Sanz2, Zihai Li1, Chrystal Paulos1, Megan Wyatt1, Diane L. Kamen3 and Gary S. Gilkeson4, 1MUSC, Charleston, SC, 2Emory University School of Medicine, Atlanta, GA, 3Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 4Department of Medicine, Medical University of South Carolina, Charleston, SC

Meeting: 2018 ACR/ARHP Annual Meeting

Keywords: B cells, Lupus and stem cells

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Session Information

Date: Monday, October 22, 2018

Title: 4M108 ACR Abstract: SLE–Etiology & Pathogenesis I (1893–1898)

Session Type: ACR Concurrent Abstract Session

Session Time: 4:30PM-6:00PM

Background/Purpose: Reports of positive effects of allogenic mesenchymal stem cells (MSCs) in treating refractory lupus, from a single center in China, led us to investigate the clinical and immune effect of a single infusion of 1×106 MSCs per kg umbilical cord MSCs in a Phase I trial of 6 patients with refractory lupus. We report the immune effects of MSC infusions on 6 patients; 5 met the primary outcome of a Systemic Lupus Response Index-4 (i.e. SRI-4). Clinical responses are submitted separately.

Methods: We assessed B and T cell subsets at Wks 0, 4, 8 and 24 by Flow. We measured levels of TGFb and glycoprotein A repetitions predominant (GARP) in the serum by ELISA as the hypothesized immune effector mechanism of MSCs. B cell assays were performed at Emory; 3 Wk. 8 samples were undeliverable due to winter storms.

Results: B cell subsets were notably affected by MSC infusion with a significant decrease in CD27 IgD double negative B cells (DN) with a concomitant increase in resting naïve B cells (rN) in 4/6 (Fig. 1). Of particular note are the diminishing subsets with an activated phenotype (CD11c+CD21-), including DN2 and activated naïve (aN) B cells. Patient 004 was the single treatment failure and her B cell subsets, with a high percentage of rN B cells and few DN/aN B cells at baseline, did not change. We assessed for changes in Tregs, Th1, Th2, TFH and Th17 subsets. 2/6 patients had increases in Tregs (i.e. patients 001, Fig. 2) and helios+ T regs (Fig. 2), but there were no major shifts in subsets as seen in B cells. GARP is highly expressed on MSCs and a major regulator of TGFb bioactivity. GARP impacts Treg development, B cell activation and development of autoimmunity. We assessed if MSC infusions impacted serum GARP or TGFb levels. There were significant increases in serum GARP (Fig. 3, p<0.01) and TGFb levels (not shown) following MSCs.

Conclusion: MSC infusions in a Phase I open label trial in refractory lupus led to clinical improvement in 5/6 patients and significant changes in immune cell subsets with a shift from activated B cell subsets to resting naïve B cells. Serum GARP and TGFb levels increased post MSC infusion serving perhaps as the proximate immune effector mediators. A Phase II double blind placebo controlled multi-center trial of UC-MSCs in 81 refractory lupus patients will be starting this summer.


Disclosure: C. Wallace Fugle, None; C. Wei, None; I. Sanz, None; Z. Li, None; C. Paulos, None; M. Wyatt, None; D. L. Kamen, None; G. S. Gilkeson, None.

To cite this abstract in AMA style:

Wallace Fugle C, Wei C, Sanz I, Li Z, Paulos C, Wyatt M, Kamen DL, Gilkeson GS. Marked Immune Cell Subset Changes in Refractory Lupus Patients in a Phase I Trial of Allogenic Mesenchymal Stem Cells [abstract]. Arthritis Rheumatol. 2018; 70 (suppl 9). https://acrabstracts.org/abstract/marked-immune-cell-subset-changes-in-refractory-lupus-patients-in-a-phase-i-trial-of-allogenic-mesenchymal-stem-cells/. Accessed .
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