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Tytuł pozycji:

Flow cytofluorometric detection of tumor-specific rosette-forming cells in patients with squamous cell carcinoma of the head and neck.

Tytuł:
Flow cytofluorometric detection of tumor-specific rosette-forming cells in patients with squamous cell carcinoma of the head and neck.
Autorzy:
Tong AW
Vanderbark AA
Kraybill W
Vetto RM
Burger DR
Źródło:
Cancer research [Cancer Res] 1982 Jul; Vol. 42 (7), pp. 2949-55.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
Język:
English
Imprint Name(s):
Publication: Baltimore, Md. : American Association for Cancer Research
Original Publication: Chicago [etc.]
MeSH Terms:
Epitopes*
Rosette Formation*
Carcinoma, Squamous Cell/*immunology
Erythrocytes/*immunology
Head and Neck Neoplasms/*immunology
Lymphocytes/*immunology
Aged ; Antigens, Neoplasm/immunology ; Flow Cytometry ; Humans ; Male ; Melanoma/immunology ; Middle Aged ; Monocytes/immunology ; Neoplasm Recurrence, Local
Substance Nomenclature:
0 (Antigens, Neoplasm)
0 (Epitopes)
Entry Date(s):
Date Created: 19820701 Date Completed: 19820814 Latest Revision: 20061115
Update Code:
20240104
PMID:
6177400
Czasopismo naukowe
Tumor-specific rosette-forming cells reactive to solubilized tumor antigens conjugated to autologous erythrocytes were quantitated by flow cytofluorometry. Leukocytes from a high frequency of the patients (greater than 70%) with squamous cell carcinoma of the head and neck (SQCC) formed rosettes to the conjugated SQCC tumor antigens but not to other histologically distinct tumor antigens (melanoma and colon carcinoma). Healthy control subjects or tumor patients with other cancers were mostly unreactive to the SQCC tumor extract [1 to 21 (5%) and 1 of 14 (7%) for controls and tumor patients, respectively]. Rosette-forming activity was observed in SQCC patients with primary cancers [22 of 30 (73%)] or in remission [5 of 6 (83%)], whereas patients with tumor recurrence were uniformly unresponsive [0 to 9 (0%)]. Tumor-specific rosette formation was mediated predominantly by monocytes, as identified by histochemical techniques and physiological properties. Rosette formation in reactive patients was abrogated by short-term culture, but the abated response could be restored by incubation with autologous serum or sera from other rosette-forming cell-positive patients. However, responsiveness of nonreactive patients with SQCC recurrence could not be constituted by rosette-forming cell-positive sera. These observations suggested the presence of tumor-reactive monocytes in a high frequency of patients with primary cancer or in remission but not in patients with recurrent disease.

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