Lethal murine graft-versus-host disease induced by donor gamma/delta expressing T cells with specificity for host nonclassical major histocompatibility complex class Ib antigens
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作者:
Blazar, BR
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
Blazar, BR
Taylor, PA
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
Taylor, PA
PanoskaltsisMortari, A
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
PanoskaltsisMortari, A
Barrett, TA
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
Barrett, TA
Bluestone, JA
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
Bluestone, JA
Vallera, DA
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机构:UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
Vallera, DA
机构:
[1] UNIV MINNESOTA HOSP, DEPT PEDIAT, DIV BONE MARROW TRANSPLANTAT, MINNEAPOLIS, MN USA
[2] UNIV MINNESOTA HOSP, DEPT THERAPEUT RADIOL, MINNEAPOLIS, MN USA
[3] NORTHWESTERN UNIV, SCH MED, DEPT MED, GASTROENTEROL SECT, CHICAGO, IL 60611 USA
[4] UNIV CHICAGO, BEN MAY INST, CHICAGO, IL 60637 USA
Although T-cell receptor (TCR) alpha/beta expressing cells have a well-known role in graft-versus-host disease (GVHD) generation, the role of TCR gamma/delta expressing cells in this process has remained unclear. To elucidate the potential function of TCR gamma/delta cells in GVHD, we have used transgenic (Tg) H-2(d) mice (termed G8) that express gamma/delta heterodimers on a high proportion of peripheral T cells. In vitro, G8 Tg gamma/delta T cells proliferate to and kill C57BL/6 (B6) (H-2(b)) which express gene products (T10(b) and T22(b)) from the nonclassical major histocompatibility complex (MHC) class Ib H-2T region. The infusion of G8 Tg (H-2T(d)) TCR gamma/delta cells into lethally irradiated [900 cGy total body irradiation (TBI)] B6 (H-2(b)) mice resulted in the generation of lethal GVHD characterized histologically by destruction of the spleen, liver, lung, and colon. Lethal GVHD was prevented by the injection of anti-TCR gamma/delta monoclonal antibodies. Immunohistochemical analysis of B6 recipients post-bone marrow transplantation (BMT) confirmed that G8 Tg TCR gamma/delta cells infiltrated GVHD target tissues (skin, liver, colon, and lung) and were absent in recipients treated with anti-TCR gamma/delta monoclonal antibodies (MoAbs) but not anti-CD4 plus anti-CD8 MoAbs. In contrast, injection of TCR gamma/delta(+) cells into irradiated (900 cGy TBI) BG.A-Tla(a) BoyEg mice that do not express either T10(b) or T22(b) did not induce lethal GVHD. Similarly, in a different GVHD system in which sublethal irradiation without bone marrow (BM) rescue was used, B6 but not B6.A-Tla(a)/BoyEg mice were found to be susceptible to TCR gamma delta(+) cell mediated GVHD-induced lethality characterized by an aplasia syndrome. These results demonstrate that TCR gamma/delta cells have the capacity to cause acute lethal GVHD in mice and suggest that nonclassical MHC class Ib gene products expressed on GVHD target organs are responsible for G8 Tg TCR gamma/delta(+) cell mediated lethality. (C) 1996 by The American Society of Hematology.