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Antibody to Mac-1 or Monocyte Chemoattractant Protein-1 Inhibits Monocyte Recruitment and Promotes Tumor Growth

  1. Author:
    Zhang, L.
    Yoshimura, T.
    Graves, D. T.
  2. Author Address

    Graves DT BOSTON UNIV MED CTR DIV ORAL BIOL SCH MED DEPT PATHOL & LAB MED 700 ALBANY ST ROOM W-202 BOSTON, MA 02118 USA BOSTON UNIV MED CTR DIV ORAL BIOL SCH MED DEPT PATHOL & LAB MED BOSTON, MA 02118 USA NCI IMMUNOPATHOL SECT IMMUNOBIOL LAB FREDERICK CANC RES & DEV CTR FREDERICK, MD 21702 USA BOSTON UNIV SCH DENT MED DIV ORAL BIOL BOSTON, MA 02118 USA
    1. Year: 1997
  1. Journal: Journal of Immunology
    1. 158
    2. 10
    3. Pages: 4855-4861
  2. Type of Article: Article
  1. Abstract:

    Human tumors are frequently infiltrated by numerous monocytes/macrophages, which can be found within the tumor mass (intratumoral) or surrounding the tumor (peritumoral). The functional role that these monocytes/macrophages play in tumor growth is controversial. To address this issue we inhibited intratumoral monocyte/macrophage recruitment with mAbs that either blocked integrin function or neutralized a tumor-produced chemotactic protein. Both treatments significantly increased tumor formation and accelerated tumor growth. Surprisingly, the same results were obtained when recruitment of peritumoral or intratumoral monocytes/macrophages was blocked. Our findings are contrary to one of the purported roles of monocytes/macrophages, particularly in the peritumoral area, since we found no evidence for monocyte/macrophage-supported tumor growth. These results provide direct evidence that intratumoral as well as peritumoral monocytes/macrophages act to limit tumor size in the early stages following tumor inoculation and provide a mechanism that accounts for monocyte/macrophage recruitment to human tumors. [References: 42]

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