Pulmonary defences to acute respiratory infection

被引:62
作者
Boyton, RJ [1 ]
Openshaw, PJ [1 ]
机构
[1] Univ London Imperial Coll Sci & Technol, Sch Med, Natl Heart & Lung Inst, St Marys Hosp, London W2 1PG, England
关键词
D O I
10.1093/bmb/61.1.1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Of all sites in the body, the lung is perhaps challenged by the greatest onslaught of microbial pathogens, many of which would cause lethal infections if unopposed. The immune response to respiratory infection must, therefore, be rapid and efficient. However, the respiratory tract is a fragile tissue with architecture that is finely designed for gas exchange, so that the price of excessive or inappropriate inflammatory responses may itself be very high. The first line of defence comes from barriers such as mucus and cilia, followed by a battery of mediators that constitute the innate response. These include lactoferrin, lysozyme, collectins and defensins. Activation of these molecules can lead directly to lysis of pathogens, or to destruction through opsonisation or the recruitment of inflammatory cells. The adaptive immune response includes the production of neutralising antibodies and the responses of T lymphocytes. Different populations of T lymphocytes may dramatically alter the balance between clearance of the pathogen and induction of tissue damage depending on the cytokines they secrete.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 39 条
[1]   Bacterial killing is enhanced by expression of lysozyme in the lungs of transgenic mice [J].
Akinbi, HT ;
Epaud, R ;
Bhatt, H ;
Weaver, TE .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5760-5766
[2]   Functionally distinct T cells in three compartments of the respiratory tract after influenza virus infection [J].
Baumgarth, N ;
Kelso, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (09) :2189-2197
[3]   Protective role of gamma interferon during the recall response to influenza virus [J].
Bot, A ;
Bot, S ;
Bona, CA .
JOURNAL OF VIROLOGY, 1998, 72 (08) :6637-6645
[4]   Local IL-4 expression in the lung reduces pulmonary influenza-virus-specific secondary cytotoxic T cell responses [J].
Bot, A ;
Holz, A ;
Christen, U ;
Wolfe, T ;
Temann, A ;
Flavell, R ;
von Herrath, M .
VIROLOGY, 2000, 269 (01) :66-77
[5]   Migration kinetics and final destination of type 1 and type 2 CD8 effector cells predict protection against pulmonary virus infection [J].
Cerwenka, A ;
Morgan, TM ;
Harmsen, AG ;
Dutton, RW .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (02) :423-434
[6]   FIELD EVALUATION OF A RESPIRATORY SYNCYTIAL VIRUS VACCINE AND A TRIVALENT PARAINFLUENZA VIRUS VACCINE IN A PEDIATRIC POPULATION [J].
CHIN, J ;
MAGOFFIN, RL ;
SHEARER, LA ;
SCHIEBLE, JH ;
LENNETTE, EH .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1969, 89 (04) :449-+
[7]   Expression of the nitric oxide synthase 2 gene is not essential for early control of Mycobacterium tuberculosis in the murine lung [J].
Cooper, AM ;
Pearl, JE ;
Brooks, JV ;
Ehlers, S ;
Orme, IM .
INFECTION AND IMMUNITY, 2000, 68 (12) :6879-6882
[8]   Collectins and pulmonary innate immunity [J].
Crouch, E ;
Hartshorn, K ;
Ofek, I .
IMMUNOLOGICAL REVIEWS, 2000, 173 :52-65
[9]   The innate immune response of the respiratory epithelium [J].
Diamond, G ;
Legarda, D ;
Ryan, LK .
IMMUNOLOGICAL REVIEWS, 2000, 173 :27-38
[10]   CD8+ T-CELL MEMORY TO VIRUSES [J].
DOHERTY, PC ;
HOU, S ;
TRIPP, RA .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (04) :545-552