Infiltration of lung carcinomas with macrophages of the 27E10-positive phenotype

被引:12
作者
Endress, H
Freudenberg, N
Fitzke, E
Grahmann, PR
Hasse, J
Dieter, P
机构
[1] TECH UNIV DRESDEN,MED FAC CARL GUSTAV CARUS,INST PHYSIOL CHEM,D-01109 DRESDEN,GERMANY
[2] UNIV FREIBURG,DEPT PATHOL,D-7800 FREIBURG,GERMANY
[3] UNIV FREIBURG,INST BIOCHEM & MOL BIOL,D-7800 FREIBURG,GERMANY
[4] UNIV FREIBURG,LUNG SURG DEPT,D-7800 FREIBURG,GERMANY
关键词
cancer; immunohistochemistry; lung; macrophages; centrifugal elutriation;
D O I
10.1016/S0169-5002(97)00042-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In order to gain insight into the role of macrophages in human lung carcinomas, we investigated material from 35 lung carcinomas and 5 healthy lungs with 4 different antibodies (CD68, MRP8, MRP14, 27E10) recognizing different macrophage subtypes. Infiltration with CD68-positive macrophages was highest and comparable in healthy lungs and lung carcinomas. Compared to healthy lungs, the infiltration of MRP8- and MRP14-positive macrophages was reduced in lung carcinomas while the number of 27E10-positive cells was enhanced. No difference in the infiltration of macrophages was observed between the different histological subtypes of carcinomas such as squamous carcinoma, small lung carcinoma, adenocarcinoma and bronchio-alveolar carcinoma. Furthermore, we present a highly suitable technique for the isolation and enrichment of macrophages from human lung carcinomas resulting in a 5-10 fold enrichment and a yield of e.g. 2-3 x 10(6) 27E10-positive macrophages/g tumor biopsy. Together with the recent findings that 27E10-positive macrophages are prevalent in early acute inflammation and release cytotoxic mediators [9] and to inhibit tumor cell proliferation [6] our findings suggest that 27E10-positive macrophages may play a role in antitumor cytotoxicity in human lung carcinomas. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:35 / 46
页数:12
相关论文
共 18 条
[11]  
MANTOVANI A, 1994, LAB INVEST, V71, P5
[12]   2 CALCIUM-BINDING PROTEINS IN INFILTRATE MACROPHAGES OF RHEUMATOID-ARTHRITIS [J].
ODINK, K ;
CERLETTI, N ;
BRUGGEN, J ;
CLERC, RG ;
TARCSAY, L ;
ZWADLO, G ;
GERHARDS, G ;
SCHLEGEL, R ;
SORG, C .
NATURE, 1987, 330 (6143) :80-82
[13]  
PAREWESCH MR, 1986, AM J PATHOL, V125, P141
[14]   DISTRIBUTION OF THE CD68 MACROPHAGE MYELOID ASSOCIATED ANTIGEN [J].
PULFORD, KAF ;
SIPOS, A ;
CORDELL, JL ;
STROSS, WP ;
MASON, DY .
INTERNATIONAL IMMUNOLOGY, 1990, 2 (10) :973-980
[15]   KP1 - A NEW MONOCLONAL-ANTIBODY THAT DETECTS A MONOCYTE MACROPHAGE ASSOCIATED ANTIGEN IN ROUTINELY PROCESSED TISSUE-SECTIONS [J].
PULFORD, KAF ;
RIGNEY, EM ;
MICKLEM, KJ ;
JONES, M ;
STROSS, WP ;
GATTER, KC ;
MASON, DY .
JOURNAL OF CLINICAL PATHOLOGY, 1989, 42 (04) :414-421
[16]   EXPRESSION OF CALCIUM-BINDING PROTEINS MRP8 AND MRP14 IS ASSOCIATED WITH DISTINCT MONOCYTIC DIFFERENTIATION PATHWAYS IN HL-60 CELLS [J].
ROTH, J ;
GOEBELER, M ;
VANDENBOS, C ;
SORG, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 191 (02) :565-570
[17]   IMMUNOHISTOCHEMICAL DEMONSTRATION OF THE CALCIUM-BINDING PROTEINS MRP8 AND MRP14 AND THEIR HETERODIMER (27E10 ANTIGEN) IN CROHNS-DISEASE [J].
SCHMID, KW ;
LUGERING, N ;
STOLL, R ;
BRINKBAUMER, P ;
WINDE, G ;
DOMSCHKE, W ;
BOCKER, W ;
SORG, C .
HUMAN PATHOLOGY, 1995, 26 (03) :334-337
[18]  
ZWADLO G, 1988, CLIN EXP IMMUNOL, V72, P510