Development and maturation of secondary lymphoid tissues

被引:509
作者
Fu, YX
Chaplin, DD
机构
[1] Washington Univ, Sch Med, Dept Pathol, Ctr Immunol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Ctr Immunol, Howard Hughes Med Inst, St Louis, MO 63110 USA
关键词
follicular dendritic cells; lymphotoxin; lymph node; Peyer's patch; tumor necrosis factor;
D O I
10.1146/annurev.immunol.17.1.399
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The secondary lymphoid tissues are located at strategic sites where foreign antigens can be efficiently brought together with immune system regulatory and effector cells. The organized structure of the secondary lymphoid tissues is thought to enhance the sensitivity of antigen recognition and to support proper regulation of the activation and maturation of the antigen-responsive lymphoid cells. Although a substantial amount is known about the cellular elements that compose the lymphoid and nonlymphoid components of the secondary lymphoid tissues, information concerning the signals that control the development of the tissues and that maintain the organized tissue microenvironment remain undefined. Studies over the past few years have identified lymphotoxin as a critical signaling molecule not only for the organogenesis of secondary lymphoid tissues but for the maintenance of aspects of their microarchitecture as well. Additional signaling molecules that contribute to the formation of normal lymphoid tissue structure are being identified at an accelerating pace. Analyses of mouse strains with congenital defects in different aspects of secondary lymphoid tissue development are beginning to clarify the role of these tissues in immune responses and host defense. This review focuses on studies defining recently identified crucial signals for the biogenesis of secondary lymphoid organs and for the maintenance of their proper microarchitecture. It also discusses new insights into how the structure of these tissues supports effective immune responses.
引用
收藏
页码:399 / 433
页数:35
相关论文
共 119 条
[41]   Hyperplasia of lymphatic vessels in VEGF-C transgenic mice [J].
Jeltsch, M ;
Kaipainen, A ;
Joukov, V ;
Meng, XJ ;
Lakso, M ;
Rauvala, H ;
Swartz, M ;
Fukumura, D ;
Jain, RK ;
Alitalo, K .
SCIENCE, 1997, 276 (5317) :1423-1425
[42]  
Kapasi ZF, 1998, J IMMUNOL, V160, P1078
[43]  
KAPASI ZF, 1993, J IMMUNOL, V150, P2648
[44]   On the key role of secondary lymphoid organs in antiviral immune responses studied in alymphoplastic (aly/aly) and spleenless (Hox11(-/-)) mutant mice [J].
Karrer, U ;
Althage, A ;
Odermatt, B ;
Roberts, CWM ;
Korsmeyer, SJ ;
Miyawaki, S ;
Hengartner, H ;
Zinkernagel, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (12) :2157-2170
[45]   A role for tumor necrosis factor receptor type 1 in gut-associated lymphoid tissue development:: Genetic evidence of synergism with lymphotoxin β [J].
Koni, PA ;
Flavell, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (12) :1977-1983
[46]   Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice [J].
Koni, PA ;
Sacca, R ;
Lawton, P ;
Browning, JL ;
Ruddle, NH ;
Flavell, RA .
IMMUNITY, 1997, 6 (04) :491-500
[47]   Distinct roles for lymphotoxin-alpha and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue [J].
Korner, H ;
Cook, M ;
Riminton, DS ;
Lemckert, FA ;
Hoek, RM ;
Ledermann, B ;
Kontgen, F ;
Fazekas de St Groth, B ;
Sedgwick, JD .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (10) :2600-2609
[48]  
KRAAL G, 1986, IMMUNOLOGY, V58, P665
[49]  
KRAAL G, 1995, AM J PATHOL, V147, P763
[50]   Chronic inflammation caused by lymphotoxin is lymphoid neogenesis [J].
Kratz, A ;
CamposNeto, A ;
Hanson, MS ;
Ruddle, NH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (04) :1461-1472