INHIBITION OF TUMOR-GROWTH BY ELIMINATION OF GRANULOCYTES

被引:257
作者
PEKAREK, LA [1 ]
STARR, BA [1 ]
TOLEDANO, AY [1 ]
SCHREIBER, H [1 ]
机构
[1] UNIV CHICAGO,DEPT ANESTHESIA & CRIT CARE,CHICAGO,IL 60637
关键词
D O I
10.1084/jem.181.1.435
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As observed for many types of cancers, heritable variants of ultraviolet light-induced tumors often grow more aggressively than the parental tumors. The aggressive growth of some variants is due to the loss of a T cell-recognized tumor specific antigen; however, other variants retain such antigens. We have analyzed an antigen retention variant and found that the variant tumor cells grow at the same rate as the parental tumor cells in vitro, but grew more rapidly than the parental cells in the T cell-deficient host. The growth of the variant cells was stimulated in vitro by factors released from tumor-induced leukocytes and by several defined growth factors. In addition, the variant cancer cells actually attracted more leukocytes in vitro than the parental cells. Furthermore, elimination of granulocytes in vivo in nude mice by a specific antigranulocyte antibody inhibited the growth of the variant cancer; indicating that this tumor requires granulocytes for rapid growth.
引用
收藏
页码:435 / 440
页数:6
相关论文
共 36 条
[1]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[2]   IMMUNOREACTIVE FIBROBLAST GROWTH-FACTOR IN CELLS OF PERITONEAL-EXUDATE SUGGESTS ITS IDENTITY WITH MACROPHAGE-DERIVED GROWTH-FACTOR [J].
BAIRD, A ;
MORMEDE, P ;
BOHLEN, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1985, 126 (01) :358-364
[3]   STIMULATION OF HUMAN PROSTATIC-CARCINOMA CELL-GROWTH BY FACTORS PRESENT IN HUMAN-BONE MARROW [J].
CHACKALROY, M ;
NIEMEYER, C ;
MOORE, M ;
ZETTER, BR .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) :43-50
[4]   MOLECULAR-CLONING OF GENE-SEQUENCES REGULATED BY PLATELET-DERIVED GROWTH-FACTOR [J].
COCHRAN, BH ;
REFFEL, AC ;
STILES, CD .
CELL, 1983, 33 (03) :939-947
[5]  
COLOMBO MP, 1992, J IMMUNOL, V149, P113
[6]  
COLOMBO MP, 1992, CANCER RES, V52, P4853
[7]   GRANULOCYTE COLONY-STIMULATING FACTOR GENE-TRANSFER SUPPRESSES TUMORIGENICITY OF A MURINE ADENOCARCINOMA INVIVO [J].
COLOMBO, MP ;
FERRARI, G ;
STOPPACCIARO, A ;
PARENZA, M ;
RODOLFO, M ;
MAVILIO, F ;
PARMIANI, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (04) :889-897
[8]   NEUTROPHILS ARE ESSENTIAL FOR EARLY ANTI-LISTERIA DEFENSE IN THE LIVER, BUT NOT IN THE SPLEEN OR PERITONEAL-CAVITY, AS REVEALED BY A GRANULOCYTE-DEPLETING MONOCLONAL-ANTIBODY [J].
CONLAN, JW ;
NORTH, RJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (01) :259-268
[9]   FIBROBLAST CELL-INTERACTIONS WITH HUMAN-MELANOMA CELLS AFFECT TUMOR-CELL GROWTH AS A FUNCTION OF TUMOR PROGRESSION [J].
CORNIL, I ;
THEODORESCU, D ;
MAN, S ;
HERLYN, M ;
JAMBROSIC, J ;
KERBEL, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6028-6032
[10]   CHARACTERIZATION OF THE MURINE ANTIGENIC DETERMINANT, DESIGNATED L3T4A, RECOGNIZED BY MONOCLONAL-ANTIBODY GK1.5 - EXPRESSION OF L3T4A BY FUNCTIONAL T-CELL CLONES APPEARS TO CORRELATE PRIMARILY WITH CLASS II MHC ANTIGEN-REACTIVITY [J].
DIALYNAS, DP ;
WILDE, DB ;
MARRACK, P ;
PIERRES, A ;
WALL, KA ;
HAVRAN, W ;
OTTEN, G ;
LOKEN, MR ;
PIERRES, M ;
KAPPLER, J ;
FITCH, FW .
IMMUNOLOGICAL REVIEWS, 1983, 74 :29-56