Reduced antigen‐presenting function of human Epstein‐Barr virus (EBV)‐B cells and monocytes after UVB radiation is accompanied by decreased expression of B7, intercellular adhesion molecule‐1 (ICAM‐1) and LFA‐3
Reduced antigen‐presenting function of human Epstein‐Barr virus (EBV)‐B cells and monocytes after UVB radiation is accompanied by decreased expression of B7, intercellular adhesion molecule‐1 (ICAM‐1) and LFA‐3
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UVB 辐射后人 Epstein-Barr 病毒 (EBV)-B 细胞和单核细胞的抗原呈递功能降低,伴随着 B7、细胞间粘附分子-1 (ICAM-1) 和 LFA-3 表达的降低
DOI:
10.1111/j.1365-2249.1995.tb03135.x
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发表时间:
1995
影响因子:
4.6
通讯作者:
M. Teunissen
中科院分区:
文献类型:
--
作者:
I. Kremer;J. D. Bos;M. Teunissen
In this study, the effect of ultraviolet‐B (UVB) radiation on antigen‐presenting function was studied, to investigate whether antigen‐presenting cells (APC) are inhibited by UVB through a common mechanism. Two types of human APC were used: EBV‐B cells and monocytes, and these were irradiated in vitro with single low doses of UVB (range 0–200 J/m2). Irradiation of EBV‐B cells or monocytes resulted in similar dose‐dependent reduction in APC function, when determined by the allogeneic mixed leucocyte reaction (MLR) or Candida albicans‐ or tetanus toxoid‐specific T cell response. Our study shows that the reduced APC function was not likely to be caused by alterations in antigen processing or cytokine production. However, UVB‐irradiated APC displayed marked changes in adhesion molecule expression. Irradiated EBV‐B cells showed reduced expression of ICAM‐1 (30%), LFA‐3 (25%) and B7‐1 (35%), white expression of HLA‐DR, CD19 and LFA‐1 was not affected. UVB irradiation of monocytes did result in reduction in the expression of HLA‐DR (30%), LFA‐3 (40%), ICAM‐1 (65%) and B7‐1 and B7‐3 (90%), but had no effect on CD14, LFA‐1 and ICAM‐3 expression. Addition of non‐irradiated cells (but not the supernatant of these cells) or CD28 antibodies partly restored T cell activation, indicating that UVB‐induced reduction in APC function is at least partly mediated via impairment of co‐stimulatory molecule expression.
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DOI:
10.1172/jci114600
发表时间:
1990-05
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
Jean Krutmann;Islam U. Khan;Robert S. Wallis;Fen Zhang;Elizabeth A. Rich;J. Ellner;C. A. Elmets
通讯作者:
Jean Krutmann;Islam U. Khan;Robert S. Wallis;Fen Zhang;Elizabeth A. Rich;J. Ellner;C. A. Elmets
DOI:
10.1111/1523-1747.ep12504877
发表时间:
1990-11
期刊:
The Journal of investigative dermatology
影响因子:
--
作者:
T. Yoshikawa;V. Rae;W. Bruins-Slot;J. V. D. Berg;J. Taylor;J. Taylor;J. Streilein
通讯作者:
T. Yoshikawa;V. Rae;W. Bruins-Slot;J. V. D. Berg;J. Taylor;J. Taylor;J. Streilein
DOI:
10.1073/pnas.90.14.6586
发表时间:
1993-07-15
影响因子:
11.1
作者:
GIMMI, CD;FREEMAN, GJ;NADLER, LM
通讯作者:
NADLER, LM
DOI:
--
发表时间:
1981
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Germain,RN
通讯作者:
Germain,RN
DOI:
--
发表时间:
1991
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Simon,JC;Tigelaar,RE;Bergstresser,PR;Edelbaum,D;CruzJr,PD
通讯作者:
CruzJr,PD