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Original communication| Volume 81, ISSUE 3, P345-350, March 1977

A new in vivo assay of human lymphocyte-mediated immunity to melanoma

  • Raymond E. Richmond
    Footnotes
    Affiliations
    From the Division of Oncology, Department of Surgery, University of California at Los Angeles School of Medicine, University of California, Los Angeles, Calif., USA

    From the Surgical Services, Sepulveda Veterans Administration Hospital, Sepulveda, Calif. USA
    Search for articles by this author
  • Courtney M. Townsend Jr.
    Footnotes
    Affiliations
    From the Division of Oncology, Department of Surgery, University of California at Los Angeles School of Medicine, University of California, Los Angeles, Calif., USA

    From the Surgical Services, Sepulveda Veterans Administration Hospital, Sepulveda, Calif. USA
    Search for articles by this author
  • Donald L. Morton
    Correspondence
    Reprint requests: Donald L. Morton, M.D., Division of Oncology, Department of Surgery, UCLA School of Medicine, The Center for Health Sciences, Los Angeles, Calif. 90024.
    Affiliations
    From the Division of Oncology, Department of Surgery, University of California at Los Angeles School of Medicine, University of California, Los Angeles, Calif., USA

    From the Surgical Services, Sepulveda Veterans Administration Hospital, Sepulveda, Calif. USA
    Search for articles by this author
  • Author Footnotes
    1 Raymond E. Richmond is a recipient of a National Institute of Health fellowship, No. CA05301-01, and Courtney M. Townsend, Jr. is the recipient of a National Institute of Health fellowship, No. CA00843-01.
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      Abstract

      Lymphocytes from melanoma patients more frequently inhibited the growth of human melanoma cells in the hamster cheek pouch than did lymphocytes from normal donors. Growth inhibition was accomplished with a much lower ratio of target cells to lymphocytes than in in vitro assays. The hamster cheek pouch assay can be used to study the relationship of blocking factors and humoral antibodies to cell-mediated immunity against human cancers.
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