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Lentiviral expression of CTLA4Ig inhibits primed xenogeneic lymphocyte proliferation and cytokine responses
Author(s) -
Mulley William R,
Wee Janet L,
Christiansen Dale,
Milland Julie,
Ierino Francesco L.,
Sandrin Mauro S.
Publication year - 2006
Publication title -
xenotransplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.052
H-Index - 61
eISSN - 1399-3089
pISSN - 0908-665X
DOI - 10.1111/j.1399-3089.2006.00297.x
Subject(s) - cytokine , cytotoxic t cell , immunology , biology , chemistry , microbiology and biotechnology , in vitro , biochemistry
Mulley WR, Wee JL, Christiansen D, Milland J, Ierino FL, Sandrin MS. Lentiviral expression of CTLA4Ig inhibits primed xenogeneic lymphocyte proliferation and cytokine responses.
Xenotransplantation 2006; 13: 248–252. © Blackwell Munksgaard, 2006 Abstract: Background: Co‐stimulatory blockade is known to inhibit lymphocyte responses and to prolong allograft and xenograft survival. The present study examines the effect of transgenic expression of cytotoxic T lymphocyte‐associated molecule‐4 immunoglobulin (CTLA4Ig) by a porcine endothelial cell line (PIEC) transduced by a lentiviral vector, on primed xenogeneic T‐cell proliferative and cytokine responses. Methods: Splenocytes from mice primed with PIEC were used as responder cells in a secondary proliferative assay. CTLA4Ig transduced and wild‐type PIEC were used as stimulator cells. Responder cells were assayed for proliferation and cytokine production. Results: Proliferation was profoundly inhibited by CTLA4Ig transduced cells compared with control cells. Cytokine analysis by enzyme linked immunospot demonstrated that production of interferon‐γ, IL4 (interleukin 4) and IL10 was inhibited by CTLA4Ig transduced cells compared with control cells. Conclusion: CTLA4Ig inhibited primed indirect xenogeneic T‐cell proliferative and cytokine responses in vitro. Expression of immunomodulatory molecules by xenogeneic tissues has potential therapeutic applications for future xenotransplantation.