Abstract
Pathologists have been aware for decades that malignant tumors can become infiltrated with significant numbers of nonmalignant stromal and lymphoreticular host cells. For certain types of malignancies, e.g., breast carcinoma, it has been claimed that the prognosis may correlate with the extent of host cell infiltration (reviewed by Underwood, 1974, and Ioachim, 1976). However, it is obvious that the light microscope has certain serious limitations when it comes to screening neoplasms for host cells. It cannot, for example, discriminate between a T or a B lymphocyte, nor can it be used as a reliable tool, as Alexander has stressed (1975), to detect certain kinds of host cells, in particular, macrophages. This fact, combined with the increasing awareness of the existence of functional subclasses of lymphocytes and macrophages (e.g., helper, killer, and suppressor T-cell subclasses), has made quantitative and qualitative studies of host cell infiltration an important feature of current tumor biology research.
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Kerbel, R.S., Twiddy, R.R., Frost, P. (1980). Host Cell Analysis of a Rapidly Metastasizing Mouse Tumor and Derived Low-Metastatic Variant Lines. In: Witz, I.P., Hanna, M.G. (eds) In Situ Expression of Tumor Immunity. Contemporary Topics in Immunobiology, vol 10. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-3677-8_11
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DOI: https://doi.org/10.1007/978-1-4684-3677-8_11
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