Infections in patients with inherited defects in phagocytic function

被引:121
作者
Andrews, T [1 ]
Sullivan, KE [1 ]
机构
[1] Childrens Hosp Philadelphia, Div Allergy & Immunol, Philadelphia, PA 19104 USA
关键词
D O I
10.1128/CMR.16.4.597-621.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Patients with defects in phagocytic function are predisposed to intracellular microorganisms and typically have early dissemination of the infection. Recognition of the underlying disorder and aggressive antimicrobial therapy has been beneficial for the patients. Improved understanding of the pathophysiolog has also affected patient management by allowing specific, targeted immunomodulatory intervention. The disorders described in this review are not common but have had a significant impact on our understanding of the role of phagocytic cells in host defense. Conversely, understanding the role of the neutrophil and macrophage in infection has benefited not just the patients described in this review but also other patients with similar disease processes.
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页码:597 / +
页数:26
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共 301 条
[1]   Anhidrotic ectodermal dysplasia associated with specific antibody deficiency [J].
Abinun, M ;
Spickett, G ;
Appleton, AL ;
Flood, T ;
Cant, AJ .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 (02) :146-147
[2]   ACTIVATION OF NADPH OXIDASE INVOLVES THE DISSOCIATION OF P21(RAC) FROM ITS INHIBITORY GDP/GTP EXCHANGE PROTEIN (RHOGDI) FOLLOWED BY ITS TRANSLOCATION TO THE PLASMA-MEMBRANE [J].
ABO, A ;
WEBB, MR ;
GROGAN, A ;
SEGAL, AW .
BIOCHEMICAL JOURNAL, 1994, 298 :585-591
[3]   Dipeptidyl peptidase I activates neutrophil-derived serine proteases and regulates the development of acute experimental arthritis [J].
Adkison, AM ;
Raptis, SZ ;
Kelley, DG ;
Pham, CTN .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (03) :363-371
[4]   ABNORMAL NEUTROPHIL CHEMOTAXIS IN GAUCHER DISEASE [J].
AKER, M ;
ZIMRAN, A ;
ABRAHAMOV, A ;
HOROWITZ, M ;
MATZNER, Y .
BRITISH JOURNAL OF HAEMATOLOGY, 1993, 83 (02) :187-191
[5]   Mycobacterium fortuitum-chelonae complex infection in a child with complete interleukin-12 receptor beta 1 deficiency [J].
Aksu, G ;
Tirpan, C ;
Cavusoglu, C ;
Soydan, S ;
Altare, F ;
Casanova, JL ;
Kutukculer, N .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2001, 20 (05) :551-553
[6]   A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency [J].
Allende, LM ;
López-Goyanes, A ;
Paz-Artal, E ;
Corell, A ;
García-Pérez, MA ;
Varela, P ;
Scarpellini, A ;
Negreira, S ;
Palenque, E ;
Arnaiz-Villena, A .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (01) :133-137
[7]   ANTIGEN-DRIVEN TISSUE-SPECIFIC SUPPRESSION FOLLOWING ORAL TOLERANCE - ORALLY-ADMINISTERED MYELIN BASIC-PROTEIN SUPPRESSES PROTEOLIPID PROTEIN-INDUCED EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS IN THE SJL MOUSE [J].
ALSABBAGH, A ;
MILLER, A ;
SANTOS, LMB ;
WEINER, HL .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2104-2109
[8]   Inherited interleukin 12 deficiency in a child with bacille Calmette-Guerin and Salmonella enteritidis disseminated infection [J].
Altare, F ;
Lammas, D ;
Revy, P ;
Jouanguy, E ;
Döffinger, R ;
Lamhamedi, S ;
Drysdale, P ;
Scheel-Toellner, D ;
Girdlestone, J ;
Darbyshire, P ;
Wadhwa, M ;
Dockrell, H ;
Salmon, M ;
Fischer, A ;
Durandy, A ;
Casanova, JL ;
Kumararatne, DS .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (12) :2035-2040
[9]   A causative relationship between mutant IFNgR1 alleles and impaired cellular response to IFNγ in a compound heterozygous child [J].
Altare, F ;
Jouanguy, E ;
Lamhamedi-Cherradi, S ;
Fondanèche, MC ;
Fizame, C ;
Ribiérre, F ;
Merlin, G ;
Dembic, Z ;
Schreiber, R ;
Lisowska-Grospierre, B ;
Fischer, A ;
Seboun, E ;
Casanova, JL .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) :723-726
[10]   Impairment of mycobacterial immunity in human interleukin-12 receptor deficiency [J].
Altare, F ;
Durandy, A ;
Lammas, D ;
Emile, JF ;
Lamhamedi, S ;
Le Deist, F ;
Drysdale, P ;
Jouanguy, E ;
Döffinger, R ;
Bernaudin, F ;
Jeppsson, O ;
Gollob, JA ;
Meinl, E ;
Segal, AW ;
Fischer, A ;
Kumararatne, D ;
Casanova, JL .
SCIENCE, 1998, 280 (5368) :1432-1435