HIV-1 GP41 BINDING-PROTEINS AND ANTIBODIES TO GP41 COULD INHIBIT ENHANCEMENT OF HUMAN RAJI CELL MHC CLASS-I AND CLASS-II EXPRESSION BY GP41

被引:20
作者
CHEN, YH
BOCK, G
VORNHAGEN, R
STEINDL, F
KATINGER, H
DIERICH, MP
机构
[1] INST HYG, A-6010 INNSBRUCK, AUSTRIA
[2] LUDWIG BOLTZMANN INST AIDS RES, INNSBRUCK, AUSTRIA
[3] INST GEN & EXPTL PATHOL, INNSBRUCK, AUSTRIA
[4] INST APPL MICROBIOL, VIENNA, AUSTRIA
[5] BIOTEST, DREIEICH, GERMANY
关键词
HIV-1; GP41; GP41-BINDING PROTEINS; ANTI-GP41; MABS; MHC EXPRESSION ENHANCEMENT;
D O I
10.1016/0161-5890(94)90092-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Based on our findings, that HIV-1 soluble gp41 could bind to several proteins on the human, T, B and monocyte cells independently of CD4, we examined the effect of HIV-1 soluble gp41 (sgp41; Env amino acids 539-684) on surface expression of MHC I and II, ICAM-1 and CD21 molecules on human Raji cells. Flow cytometry (FACS) analysis demonstrated that sgp41 could selectively enhance MHC class I and II expression on Raji cells, but did not increase expression of other cell surface antigens, such as, CD21 and CD54 (ICAM-1). Soluble gp41 could also enhance MHC class I and II expression on another human B cell line, Bjab. The sgp41-dependent enhancement of the MHC class I and II expression on Raji cells is time- and dose-dependent. The sgp41 enhancement effect on the MHC antigen expression could be inhibited by the gp41-binding proteins of 45, 49 and 62 kD (isolated from Raji-lysate) which could inhibit the sgp41-binding to Raji cells. Interestingly, this sgp41-dependent enhancement of the MHC class I and II expression could also be inhibited by two mAbs to HIV-1 gp41, but not by a third mAb binding to a different site on gp41. These results demonstrate that HIV-I sgp41 can selectively enhance the human Raji cell MHC class I and II antigen expression and this enhancement effect could be inhibited by the sgp41-binding proteins and anti-gp41 antibodies, and suggest that the sgp41-dependent enhancement is mediated by its binding to Raji membrane proteins of 45, 49 and 62 kD.
引用
收藏
页码:977 / 982
页数:6
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