MACROPHAGES IN EXPERIMENTAL AND HUMAN-BRAIN TUMORS .2. STUDIES OF THE MACROPHAGE CONTENT OF HUMAN-BRAIN TUMORS

被引:201
作者
MORANTZ, RA [1 ]
WOOD, GW [1 ]
FOSTER, M [1 ]
CLARK, M [1 ]
GOLLAHON, K [1 ]
机构
[1] UNIV KANSAS,MED CTR,COLL HLTH SCI & HOSP,DEPT PATHOL,KANSAS CITY,KS 66103
关键词
D O I
10.3171/jns.1979.50.3.0305
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The authors have analyzed 47 tumors of the central nervous system (11 glioblastomas, nine meningiomas, three medulloblastomas, 12 assorted primary neural tumors, and 12 brain metastases) for their content of macrophages. Cell suspensions were prepared by enzymatic digestion and macrophages were quantitated by IgGEAC rosette formation. Adsorption of sensitized indicator cells (EA) to sections of tumor was used as a measure to determine the distribution of IgGFc receptor-positive cells within the tumors and to serve as a control for selective release of IgGFc receptor-positive cells by enzyme digestion. The 11 glioblastomas had a mean macrophage content of 45% (range: 8% to 78%), the nine meningiomas had a mean of 44% (range: 5% to 81%), the three medulloblastomas a mean of 6% (range: 2% to 15%), and the metastatic tumors a mean of 24% (range: 4% to 70%). Adsorption of EA demonstrated that IgGFc receptor-positive cells were distributed throughout the tumor mass, although different types of patterns were observed. There was an excellent correlation between the percent of IgGEAC positive cells in suspension and the extent of EA adsorption to the tumor sections. Compared to systemic neoplasms, most nervous system tumors have a high macrophage content. It is possible that the high macrophage content of brain tumors is related to their immunogenicity, and may be a partial explanation for the rarity of brain-tumor metastases.
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页码:305 / 311
页数:7
相关论文
共 21 条
[1]  
BROOKS WH, 1974, SURG NEUROL, V2, P419
[2]   LYMPHOCYTIC INFILTRATION IN LONG SURVIVAL GLIOBLASTOMAS - POSSIBLE HOSTS RESISTANCE [J].
DILORENZO, N ;
PALMA, L ;
NICOLE, S .
ACTA NEUROCHIRURGICA, 1977, 39 (1-2) :27-33
[3]   SEQUESTRATION OF MACROPHAGES IN GROWING TUMORS AND ITS EFFECT ON IMMUNOLOGICAL CAPACITY OF HOST [J].
ECCLES, SA ;
ALEXANDER, P .
BRITISH JOURNAL OF CANCER, 1974, 30 (01) :42-49
[4]   MONOCYTOSIS ASSOCIATED WITH GROWTH OF TRANSPLANTED SYNGENEIC RAT SARCOMATA DIFFERING IN IMMUNOGENICITY [J].
ECCLES, SA ;
BANDLOW, G ;
ALEXANDER, P .
BRITISH JOURNAL OF CANCER, 1976, 34 (01) :20-27
[5]   MACROPHAGE CONTENT OF TUMORS IN RELATION TO METASTATIC SPREAD AND HOST IMMUNE-REACTION [J].
ECCLES, SA ;
ALEXANDER, P .
NATURE, 1974, 250 (5468) :667-669
[6]  
FUJITA S, 1976, PROGR NEUROPATHOLOGY, V3, P1
[7]   CELL-MEDIATED IMMUNITY AND BLOCKING FACTORS IN PATIENTS WITH TUMORS OF CENTRAL NERVOUS-SYSTEM [J].
KUMAR, S ;
TAYLOR, G ;
STEWARD, JK ;
WAGHE, MA ;
MORRISJO.P .
INTERNATIONAL JOURNAL OF CANCER, 1973, 12 (01) :194-205
[8]  
LEVY NL, 1972, CANCER RES, V32, P477
[9]   IMMUNOBIOLOGY OF PRIMARY INTRACRANIAL TUMORS .1. STUDIES OF CELLULAR AND HUMORAL GENERAL IMMUNE COMPETENCE OF BRAIN-TUMOR PATIENTS [J].
MAHALEY, MS ;
BROOKS, WH ;
ROSZMAN, TL ;
BIGNER, DD ;
DUDKA, L ;
RICHARDSON, S .
JOURNAL OF NEUROSURGERY, 1977, 46 (04) :467-476
[10]   ANTIBODY-MEDIATED HEMADSORPTION BY TUMOR TISSUES [J].
MILGROM, F ;
HUMPHREY, LJ ;
TONDER, O ;
YASUDA, J ;
WITEBSKY, E .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1968, 33 (05) :478-&