Complement evasion by human pathogens

被引:567
作者
Lambris, John D. [1 ]
Ricklin, Daniel [1 ]
Geisbrecht, Brian V. [2 ]
机构
[1] Univ Penn, Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Univ Missouri Kansas City, Sch Biol Sci, Div Cell Biol & Biophys, Kansas City, MO 64110 USA
关键词
D O I
10.1038/nrmicro1824
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human immune system has developed an elaborate network of cascades for dealing with microbial intruders. Owing to its ability to rapidly recognize and eliminate microorganisms, the complement system is an essential and efficient component of this machinery. However, many pathogenic organisms have found ways to escape the attack of complement through a range of different mechanisms. Recent discoveries in this field have provided important insights into these processes on a molecular level. These vital developments could augment our knowledge of the pathology and treatment of infectious and inflammatory diseases.
引用
收藏
页码:132 / 142
页数:11
相关论文
共 106 条
[81]   Anti-opsonic properties of staphylokinase [J].
Rooijakkers, SHM ;
van Wamel, WJB ;
Ruyken, M ;
van Kessel, KPM ;
van Strijp, JAG .
MICROBES AND INFECTION, 2005, 7 (03) :476-484
[82]   Staphylococcal complement inhibitor: Structure and active sites [J].
Rooijakkers, Suzan H. M. ;
Milder, Fin J. ;
Bardoel, Bart W. ;
Ruyken, Maartje ;
van Strijp, Jos A. G. ;
Gros, Piet .
JOURNAL OF IMMUNOLOGY, 2007, 179 (05) :2989-2998
[83]   Bacterial complement evasion [J].
Rooijakkers, Suzan H. M. ;
van Strijp, Jos A. G. .
MOLECULAR IMMUNOLOGY, 2007, 44 (1-3) :23-32
[84]   Variola virus immune evasion design: Expression of a highly efficient inhibitor of human complement [J].
Rosengard, AM ;
Liu, Y ;
Nie, ZP ;
Jimenez, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8808-8813
[85]   The structure of OMCI, a novel lipocalin inhibitor of the complement system [J].
Roversi, Pietro ;
Lissina, Olga ;
Johnson, Steven ;
Ahmat, Nurfilza ;
Paesen, Guido C. ;
Ploss, Kerstin ;
Boland, Wilhelm ;
Nunn, Miles A. ;
Lea, Susan M. .
JOURNAL OF MOLECULAR BIOLOGY, 2007, 369 (03) :784-793
[86]   Kinetic analysis of glycoprotein C of herpes simplex virus types 1 and 2 binding to heparin, heparan sulfate, and complement component C3b [J].
Rux, AH ;
Lou, H ;
Lambris, JD ;
Friedman, HM ;
Eisenberg, RJ ;
Cohen, GH .
VIROLOGY, 2002, 294 (02) :324-332
[87]   Interaction of glycoprotein H of human herpesvirus 6 with the cellular receptor CD46 [J].
Santoro, F ;
Greenstone, HL ;
Insinga, A ;
Liszewski, MK ;
Atkinson, JP ;
Lusso, P ;
Berger, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25964-25969
[88]   CRYSTAL-STRUCTURE OF THE C2 FRAGMENT OF STREPTOCOCCAL PROTEIN-G IN COMPLEX WITH THE FC DOMAIN OF HUMAN-IGG [J].
SAUERERIKSSON, AE ;
KLEYWEGT, GJ ;
UHL, M ;
JONES, TA .
STRUCTURE, 1995, 3 (03) :265-278
[89]   A macrophage invasion mechanism of pathogenic mycobacteria [J].
Schorey, JS ;
Carroll, MC ;
Brown, EJ .
SCIENCE, 1997, 277 (5329) :1091-1093
[90]   Electrostatic modeling predicts the activities of orthopoxvirus complement control proteins [J].
Sfyroera, G ;
Katragadda, M ;
Morikis, D ;
Isaacs, SN ;
Lambris, JD .
JOURNAL OF IMMUNOLOGY, 2005, 174 (04) :2143-2151