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  Vol. 125 No. 2, February 1990 TABLE OF CONTENTS
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  PAPERS READ BEFORE THE ANNUAL MEETING OF THE SOCIETY OF SURGICAL ONCOLOGY, SAN FRANCISCO, CALIF, MAY 21 TO MAY 24, 1989-PART I
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Patterns of Human Tumor-Infiltrating Lymphocytes in 120 Human Cancers

Charles M. Balch, MD; Lee B. Riley, MD; Yoon Joo Bae, MD; Marie A. Salmeron, MD; Chris D. Platsoucas, PhD; Andrew von Eschenbach, MD; Kyogo Itoh, MD

Arch Surg. 1990;125(2):200-205.


Abstract

• Tumor-infiltrating lymphocytes from 120 samples of human cancers, including melanoma, renal cell carcinoma, breast cancer, sarcoma, and colon cancer, were examined. The percentage of lymphocytes recovered from the cancer varied widely; that of renal cell carcinoma was higher than that of breast or colon cancer (65% vs 45%), which was higher than that of melanomas or sarcomas (30% to 35%). The types of lymphocytes before and after interleukin 2 activation showed specific patterns. CD4+ helper T cells predominated in all tumors except melanomas, which had more CD8+ cytotoxic T cells. CD16+ natural killer cells were recovered in renal cell carcinoma and sarcomas. Three different cytotoxic lymphocytes were identified among interleukin 2–activated tumor-infiltrating lymphocytes: (1) CD3+ CD16 cytotoxic T lymphocytes with cytotoxicity restricted to autologous tumor cells in melanomas, (2) CD3 CD16+ natural killer cells with vigorous major histocompatibility complex–nonrestricted cytotoxicity in renal cell carcinoma, and (3) CD3+ CD16 T cells with modest levels of major histocompatibility complex–nonstricted cytotoxicity in all cancers except melanomas. Thus, there was considerable diversity of tumor-infiltrating lymphocytes among these histologically distinct tumors with respect to magnitude of lymphocyte infiltration, phenotypic expression, and functional capacity.

(Arch Surg. 1990;125:200-205)



Author Affiliations

From the Departments of General Surgery (Drs Balch, Riley, Bae, Salmeron, and Itoh), Immunology (Drs Platsoucas and Itoh), and Urology (Dr von Eschenbach), The University of Texas M. D. Anderson Cancer Center, Houston.


Footnotes

Accepted for publication November 15, 1989.

Read before the annual meeting of the Society of Surgical Oncology, San Francisco, Calif, May 21, 1989.

Reprint requests to Department of General Surgery, The University of Texas M. D. Anderson Cancer, 1515 Holcombe Blvd, HMB 106, Houston, TX 77030 (Dr Balch).



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