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Clinical-scale Rapid Autologous BK-virus Specific T Cell Line generation from Kidney Transplant Recipients with Active Viremia for Adoptive Immunotherapy.

Clinical-scale Rapid Autologous BK-virus Specific T Cell Line generation from Kidney Transplant Recipients with Active Viremia for Adoptive Immunotherapy.
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Lamarche C, Orio J, Georges-Tobar V, Pincez T, Goupil M, Dahmani A, Carli C C, Brasey A, Busque L, Delisle JS,


Lamarche C, Orio J, Georges-Tobar V, Pincez T, Goupil M, Dahmani A, Carli C C, Brasey A, Busque L, Delisle JS, (click to view)

Lamarche C, Orio J, Georges-Tobar V, Pincez T, Goupil M, Dahmani A, Carli C C, Brasey A, Busque L, Delisle JS,

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Transplantation 2017 02 23() doi 10.1097/TP.0000000000001698
Abstract
BACKGROUND
Polyomavirus-associated nephropathy (PVAN) following BK virus reactivation in kidney transplant recipients (KTR) can compromise graft survival. Lowering immunosuppression is the only established approach to prevent or treat PVAN but nonspecifically increasing host immune competence also augments rejection risk. Ex vivo T cell stimulation/expansion offers the possibility to generate BK-specific T cell lines for adoptive immunotherapy. The objective of this study was to develop and characterize a clinical scale protocol to generate BK-specific T cell lines from viremic KTR.

METHODS
Peripheral blood mononuclear cells from healthy controls (HC) and viremic KTR were stimulated using BK-virus peptide libraries loaded or not on monocytes-derived dendritic cells. Cell counts, flow cytometry and next-generation sequencing were used to assess T cell expansion, differentiation and clonal diversity. Enzyme-linked immunospots, cytotoxicity assays as well as adoptive transfer in NOD/SCID/IL2Rγnull (NSG) mice were used to assess for pathogen-specificity and evidence of nonspecific alloreactivity.

RESULTS
T cell lines from KTR and HC showed similar characteristics, implying that ongoing immunosuppression and chronic virus exposure do not compromise the differentiation, specificity or clonal diversity of T cell lines following ex vivo production. Using antigen-loaded dendritic cells improved T cell expansion, favored central memory T cell differentiation. The T cell lines were antigen-specific and showed no nonspecific alloreactivity in vitro and in vivo.

CONCLUSIONS
Using a rapid, clinically-compliant culture system, we show that autologous BK virus-specific T cell lines can be reliably generated from viremic KTR. Our results pave the way for the treatment or prevention of PVAN with adoptive immunotherapy.

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