INDUCIBLE ACCESSORY FUNCTION OF A MACROPHAGE CELL-LINE

被引:1
作者
AIELLO, FB
GUSELLA, L
LONGO, DL
BIRCHENALLROBERTS, M
TAKACS, L
TAKEI, F
RUSCETTI, F
MUSIANI, P
DURUM, SK
机构
[1] CONSORZIO MARIO NEGRI S,IST RIC FARMACOL & BIOMED MARIO NEGRI,I-66030 SANTA MARIA IMBAR,ITALY
[2] NCI,FREDERICK CANC RES & DEV CTR,BIOL RESPONSE MODIFIERS PROGRAM,FREDERICK,MD 21701
[3] CANC CONTROL AGCY,VANCOUVER V5Z 3J3,BC,CANADA
关键词
D O I
10.3109/08923979309035232
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Costimulatory molecules in addition to occupancy of the T-cell antigen receptor, are required to induce T-cell proliferation.Previous work suggested that membrane molecules responsible for costimulatory activity were not constitutively expressed on the antigen presenting cell (APC) surface. In the present study, we have identified a cloned macrophage cell line (FLJ2) with inducible APC function. The unactivated FLJ2 line could not induce T-cell proliferation. FLJ2 could present alloantigen, and stimulate proliferation of either a T-cell clone or normal resting T cells following activation with IFN gamma or unexpectedly with lipopolysaccaride (LPS)-Activated FLJ2 cells could be fixed and APC function was preserved. The relevant inducible molecules required for APC function appeared distinct from Ia and IL1. The expression of ICAM-1 and LFA-1 was increased during activation and anti-LFA-1 antibody blocked APC function. This suggests that one important feature of the activation process may be improvement of cellular adhesion.
引用
收藏
页码:327 / 353
页数:27
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