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Society of University Surgeons| Volume 74, ISSUE 2, P190-197, August 1973

The immunogenetics of the major histocompatibility chromosomal region in man

  • H.F. Seigler
    Correspondence
    Reprint requests: Dr. H. F. Seigler, Box 3052, Duke University Medical Center, Durham, N. C. 27710.
    Affiliations
    From the Department of Surgery and Division of Immunology, Duke University Medical Center Durham, N. C., U.S.A.

    From the Durham Veterans Administration Hospital, Durham, N. C., U.S.A.
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  • F.E. Ward
    Affiliations
    From the Department of Surgery and Division of Immunology, Duke University Medical Center Durham, N. C., U.S.A.

    From the Durham Veterans Administration Hospital, Durham, N. C., U.S.A.
    Search for articles by this author
  • D.B. Amos
    Affiliations
    From the Department of Surgery and Division of Immunology, Duke University Medical Center Durham, N. C., U.S.A.

    From the Durham Veterans Administration Hospital, Durham, N. C., U.S.A.
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  • D.L. Stickel
    Affiliations
    From the Department of Surgery and Division of Immunology, Duke University Medical Center Durham, N. C., U.S.A.

    From the Durham Veterans Administration Hospital, Durham, N. C., U.S.A.
    Search for articles by this author
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      Abstract

      The major histocompatibility locus in man has been named HL-A and the mixed lymphocyte reaction (MLC) has been felt to be an in vitro measure of the locus. In this report we propose a more complex histocompatibility system and term this the HL-1 chromosomal region. Results suggest that the MLC locus is linked to HL-A and not a product of the HL-A locus itself. Studies in a family in which recombination between the genes determining the antigens of the first and second HL-A loci were observed suggested that the locus controlling this reaction was closely linked to the second HL-A locus; differences involving second-series antigens provoked strong stimulation but first-locus antigenic differences did not. Linkage of immune response genes (Ir) is suggested by the correlation of HL-A with mean skin allograft survival times (MST) in families. The skin graft survival times were not always predictable by the degree of MLC stimulation. The absence of absolute correlation of allograft survival with either HL-A or MLC suggests that a genetic factor (Ir) linked to HL-A rather than HL-A itself might provide primary control of delayed-type hypersensitivity and that HL-A, MLC, and Ir comprise a series of closely linked loci that make up the majority transplantation region in man—HL-1.
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