SEQUESTRATION FROM IMMUNE CD4+ T-CELLS OF MYCOBACTERIA GROWING IN HUMAN MACROPHAGES

被引:171
作者
PANCHOLI, P
MIRZA, A
BHARDWAJ, N
STEINMAN, RM
机构
[1] Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York
关键词
D O I
10.1126/science.8098550
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
CD4+ helper T cells mediate resistance to tuberculosis, presumably by enhancing the antimicrobial activity of macrophages within which the Mycobacterium tuberculosis organism grows. A first step in resistance should be the presentation of mycobacterial antigens by macrophages to CD4+ T cells. However, when the antigenic stimulus is limited to organisms growing in human monocytes, the organisms become sequestered from immune CD4+ T cells. This block in presentation is selective for growing mycobacteria and not for other stimuli. Sequestration would allow replicating organisms to persist in infected individuals and may contribute to virulence.
引用
收藏
页码:984 / 986
页数:3
相关论文
共 24 条
[1]  
BAHR GM, 1981, IMMUNOLOGY, V44, P593
[2]   TUBERCULOSIS IN PATIENTS WITH HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION [J].
BARNES, PF ;
BLOCH, AB ;
DAVIDSON, PT ;
SNIDER, DE .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (23) :1644-1650
[3]   THE PROCESSING AND PRESENTATION OF MYCOBACTERIAL ANTIGENS BY HUMAN-MONOCYTES [J].
BHARDWAJ, V ;
COLSTON, MJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (05) :691-696
[4]  
BRODSKY FM, 1991, ANNU REV IMMUNOL, V9, P707
[5]   EVIDENCE THAT VESICLES CONTAINING LIVING, VIRULENT MYCOBACTERIUM-TUBERCULOSIS OR MYCOBACTERIUM-AVIUM IN CULTURED HUMAN MACROPHAGES ARE NOT ACIDIC [J].
CROWLE, AJ ;
DAHL, R ;
ROSS, E ;
MAY, MH .
INFECTION AND IMMUNITY, 1991, 59 (05) :1823-1831
[6]   AN OUTBREAK OF TUBERCULOSIS WITH ACCELERATED PROGRESSION AMONG PERSONS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS - AN ANALYSIS USING RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS [J].
DALEY, CL ;
SMALL, PM ;
SCHECTER, GF ;
SCHOOLNIK, GK ;
MCADAM, RA ;
JACOBS, WR ;
HOPEWELL, PC .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (04) :231-235
[7]  
DANNENBERG AM, 1984, MYCOBACTERIA SOURCEB, P721
[8]  
ELLNER JJ, 1978, J IMMUNOL, V121, P2573
[9]  
ELLNER JJ, 1989, REV INFECT DIS, V11, pS455
[10]  
FUJIWARA H, 1991, IMMUNOLOGY, V72, P194