Nasal-associated lymphoid tissue is a mucosal inductive site for virus-specific humoral and cellular immune responses

被引:151
作者
Zuercher, AW
Coffin, SE
Thurnheer, MC
Fundova, P
Cebra, JJ
机构
[1] Univ Penn, Dept Biol, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pediat, Sch Med, Philadelphia, PA 19104 USA
[3] Acad Sci Czech Republ, Inst Microbiol, Div Immunol & Gnotobiol, Prague, Czech Republic
关键词
D O I
10.4049/jimmunol.168.4.1796
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peyer's patches are known as mucosal inductive sites for humoral and cellular immune responses in the gastrointestinal tract. In contrast, functionally equivalent structures in the respiratory tract remain elusive. It has been suggested that nasal-associated lymphoid tissue (NALT) might serve as a mucosal inductive site in the upper respiratory tract. However, typical signs of mucosal inductive sites like development of germinal center reactions after Ag stimulation and isotype switching of naive B cells to IgA production have not been directly demonstrated. Moreover, it is not known whether CTL can be generated in NALT. To address these issues, NALT was structurally and functionally analyzed using a model of intranasal infection of C3H mice with reovirus. FACS and histological analyses revealed development of germinal centers in NALT in parallel with generation and expansion of IgA(+) and IgG2a(+) B cells after intranasal reovirus infection. Reovirus-specific IgA was produced in both the upper respiratory and the gastrointestinal tract, whereas production of reovirus-specific IgG2a was restricted to NALT, submandibular, and mesenteric lymph nodes. Moreover, virus-specific CTL were detected in NALT. Limiting dilution analysis showed a 5- to 6-fold higher precursor CTL frequency in NALT compared with a cervical lymph node. Together these data provide direct evidence that NALT is a mucosal inductive site for humoral and cellular immune responses in the upper respiratory tract.
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页码:1796 / 1803
页数:8
相关论文
共 46 条
[1]   IgA antibody-forming cell responses in the nasal-associated lymphoid tissue of mice vaccinated by intranasal, intravenous and/or subcutaneous administration [J].
Asanuma, H ;
Aizawa, C ;
Kurata, T ;
Tamura, S .
VACCINE, 1998, 16 (13) :1257-1262
[2]   Isolation and characterization of mouse nasal-associated lymphoid tissue [J].
Asanuma, H ;
Thompson, AH ;
Iwasaki, T ;
Sato, Y ;
Inaba, Y ;
Aizawa, C ;
Kurata, T ;
Tamura, SI .
JOURNAL OF IMMUNOLOGICAL METHODS, 1997, 202 (02) :123-131
[3]   Circulating immunoglobulin G can play a critical role in clearance of intestinal reovirus infection [J].
Barkon, ML ;
Haller, BL ;
Virgin, HW .
JOURNAL OF VIROLOGY, 1996, 70 (02) :1109-1116
[4]  
Bellum SC, 1996, LAB INVEST, V74, P221
[5]  
BIENENSTOCK J, 1999, MUCOSAL IMMUNOLOGY, P283
[6]  
BRUNNER KT, 1976, IN VITRO METHODS CEL, P423
[7]  
BUTCHER EC, 1982, J IMMUNOL, V129, P2698
[8]   Nasal-associated lymphoid tissue is an inductive site for rat tear IgA antibody responses [J].
Carr, RM ;
Lolachi, CM ;
Albaran, RG ;
Ridley, DM ;
Montgomery, PC ;
OSullivan, NL .
IMMUNOLOGICAL INVESTIGATIONS, 1996, 25 (5-6) :387-396
[9]   SELECTIVE BINDING AND TRANSCYTOSIS OF ULEX-EUROPAEUS-1 LECTIN BY MOUSE PEYERS-PATCH M-CELLS IN-VIVO [J].
CLARK, MA ;
JEPSON, MA ;
SIMMONS, NL ;
HIRST, BH .
CELL AND TISSUE RESEARCH, 1995, 282 (03) :455-461
[10]   PEYERS PATCHES - ENRICHED SOURCE OF PRECURSORS FOR IGA-PRODUCING IMMUNOCYTES IN RABBIT [J].
CRAIG, SW ;
CEBRA, JJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (01) :188-&