Targeting cell-surface VISTA expression on allospecific naïve T cells promotes tolerance
The success of allogeneic hematopoietic stem cell transplantation (allo-HSCT) can be limited by graft-versus-host disease (GVHD). T-cell activation is a key factor in GVHD progression. Costimulatory signals can be counterbalanced by coinhibitory signals such as the checkpoint molecule VISTA (V-domain immunoglobulin-containing suppressor of T-cell activation)/programmed death-1 homolog that restrains activation and maintains donor T-cell quiescence. A single dose of anti-VISTA monoclonal antibody (mAb) prevents acute GVHD lethality in multiple models. Naïve donor T cells express moderate VISTA levels, which transiently increase in allo-HSCT recipients in association with T-cell receptor signaling, leading to heightened susceptibility to anti-VISTA mAb-mediated depletion, in contrast to donor T cells transferred to syngeneic recipients. Anti-VISTA mAb donor T-cell depletion was compatible with rapamycin but incompatible with peritransplant tacrolimus GVHD prophylaxis. Targeting VISTA exclusively on host cells or donor CD8+ T cells was not protective against GVHD lethality. Instead, anti-VISTA mAb-mediated deletion of alloreactive donor T cells depended on targeting a third (non-T) cell type. Further mechanistic studies indicated that donor T cells concurrently exposed to anti-VISTA mAb in vivo but not preincubated in vitro before adoptive T-cell transfer were eliminated via Fc receptor (FcR)-mediated phagocytosis. In a lymphoma challenge model, a graft-versus-lymphoma (GVL) effect was fully retained when anti-human VISTA mAb exclusively targeted donor CD4+ T cells, and was delayed but mostly retained when unseparated donor T cells were infused. In a xenogeneic GVHD model, anti-human VISTA mAb reduced donor T-cell expansion, VISTA T-cell expression levels, and recipient lethality. Together, these data support a novel clinical translational pathway in which acute GVHD lethality can be mitigated without negating the GVL effect.
Authors
- Michael Zaiken (ORCID: https://orcid.org/0000-0001-6971-3170)
- Wilson L. Davis
- Brent H. Koehn (ORCID: https://orcid.org/0000-0002-3669-2702)
- Kyle D. Smith (ORCID: https://orcid.org/0000-0002-6546-2383)
- Cindy Eide (ORCID: https://orcid.org/0000-0001-7314-2550)
- Isabelle Le Mercier (ORCID: https://orcid.org/0000-0002-2422-5170)
- Michael J. Molloy
- Asim Saha (ORCID: https://orcid.org/0000-0003-4721-2695)
- Angela Panoskaltsis‐Mortari (ORCID: https://orcid.org/0000-0003-1802-1785)
- Catherine Carrière (ORCID: https://orcid.org/0000-0002-3119-1247)
- Randolph J. Noelle (ORCID: https://orcid.org/0000-0002-2222-2136)
- Megan Riddle (ORCID: https://orcid.org/0000-0002-9557-217X)
- Tae Kon Kim (ORCID: https://orcid.org/0000-0002-5182-3870)
- Bruce R. Blazar (ORCID: https://orcid.org/0000-0002-9608-9841)
- Jakub Tolar (ORCID: https://orcid.org/0000-0002-0957-4380)
- Elizabeth C. Nowak (ORCID: https://orcid.org/0000-0001-8791-6166)
- Keli L. Hippen
- Jay L. Rothstein
- Jeremy Allred
- N. Schwertner
- Y H Peng (ORCID: https://orcid.org/0009-0004-1477-1225)
- Sladjana Skopalja-Gardner
Institutions
- Dartmouth College (US)
- University of Minnesota (US)
- University of Minnesota System (US)
- OSE Immunotherapeutics (France) (FR)
- Dartmouth Psychiatric Research Center (US)
- University of Minnesota Medical Center (US)
- IDEX Corporation (United States) (US)
- C4 Therapeutics (United States) (US)
- Dartmouth Cancer Center
- Vanderbilt University Medical Center (US)
Publication Details
- Journal
- Blood
- Published
- 2025-02-07
- DOI
- https://doi.org/10.1182/blood.2024025884
- Citations
- 5
- Primary Topic
- Hematopoietic Stem Cell Transplantation
- Type
- article
- Field-Weighted Citation Impact
- 8.85