MEDIATION OF ACUTE BUT NOT CHRONIC REJECTION OF MHC-INCOMPATIBLE RAT-KIDNEY GRAFTS BY ALLOREACTIVE CD4 T-CELLS ACTIVATED BY THE DIRECT PATHWAY OF SENSITIZATION
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BRAUN, MY
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLAND
BRAUN, MY
[1
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MCCORMACK, A
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLAND
MCCORMACK, A
[1
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WEBB, G
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLAND
WEBB, G
[1
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BATCHELOR, JR
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HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLANDHAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLAND
BATCHELOR, JR
[1
]
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[1] HAMMERSMITH HOSP,ROYAL POSTGRAD MED SCH,DEPT IMMUNOL,DUCANE RD,LONDON W12 0NN,ENGLAND
It has been previously postulated that there are two pathways of sensitization of MHC-incompatible kidney allografts: a direct pathway in which the host responder T cells are activated by MHC-incompatible passenger dendritic cells of the graft, and an indirect pathway, in which graft alloantigens are processed like ''nominal' T cell antigens by host accessory cells, and presented as self-MHC restricted moieties. We show here that a rat AS anti-August alloreactive CD4+ T cell line, and a presumptive clone, activated through the direct pathway are capable in an adoptive transfer model of initiating rejection of normal August kidney grafts. However, neither the T cell line nor the presumptive clone initiates rejection of passenger cell-depleted August kidneys. The results support the hypothesis that direct pathway-sensitized T cells play a dominant role in early acute rejection, but not in chronic rejection.
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
BRIDEAU, RJ
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CARTER, PB
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
CARTER, PB
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MCMASTER, WR
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
MCMASTER, WR
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MASON, DW
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
MASON, DW
;
WILLIAMS, AF
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
BRIDEAU, RJ
;
CARTER, PB
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
CARTER, PB
;
MCMASTER, WR
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
MCMASTER, WR
;
MASON, DW
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND
MASON, DW
;
WILLIAMS, AF
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UNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLANDUNIV OXFORD,SIR WILLIAM DUNN SCH PATHOL,MRC,CELLULAR IMMUNOL UNIT,OXFORD OX1 3RE,ENGLAND