The common mucosal immune system: from basic principles to enteric vaccines with relevance for the female reproductive tract.
The common mucosal immune system: from basic principles to enteric vaccines with relevance for the female reproductive tract.
复制标题
常见的粘膜免疫系统:从基本原理到与女性生殖道相关的肠道疫苗。
DOI:
10.1071/rd9940369
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发表时间:
1994
期刊:
影响因子:
--
通讯作者:
Kiyono,H
中科院分区:
文献类型:
--
作者:
McGhee,JR;Xu-Amano,J;Miller,CJ;Jackson,RJ;Fujihashi,K;Staats,HF;Kiyono,H
The realization that induction of immune responses at mucosal surfaces may prevent colonization, invasion or dissemination of pathogenic microorganisms has spurred intensive efforts to develop vaccines which elicit effective mucosal immunity. In this paper, recent results are discussed for mice given cholera toxin as both an immunogen and as an adjuvant for inducing both humoral and gastrointestinal mucosal immune responses. Oral administration of cholera toxin alone or with a co-administered protein vaccine tetanus toxoid induces a strong T helper type 2 (TH2) cell response in both Peyer's patches and spleen. Both serum IgG and secretory IgA antibodies specific for cholera toxin or for the co-administered protein tetanus toxoid were induced. When administered parentally, however, no mucosal antibody responses were evident and a mixed TH1- and TH2-type CD4+ T cell response was noted in the spleen. Various vectors are being employed in an effort not only to induce mucosal immune responses but also to direct the response to a TH1-type response, thought to promote strong cell-mediated immune responses, or to a TH2-type response for maximum B cell antibody responses. The ability to manipulate the TH cell responses may provide a more rational approach for the design of vaccines. Although lymphoid tissues of the female reproductive tract differ from that of the gut, many of the strategies and evolving principles may be directly applicable to the development of vaccines designed to prevent sexually transmitted diseases.
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影响因子:
4.4
作者:
T. Mosmann;H. Cherwinski;M. Bond;M. Giedlin;R. Coffman
通讯作者:
T. Mosmann;H. Cherwinski;M. Bond;M. Giedlin;R. Coffman
影响因子:
64.8
作者:
C. Wira;C. Sandoe
通讯作者:
C. Sandoe
DOI:
--
发表时间:
1990
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Taguchi,T;McGhee,JR;Coffman,RL;Beagley,KW;Eldridge,JH;Takatsu,K;Kiyono,H
通讯作者:
Kiyono,H
DOI:
--
发表时间:
1987
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Murray,PD;McKenzie,DT;Swain,SL;Kagnoff,MF
通讯作者:
Kagnoff,MF
DOI:
--
发表时间:
1990
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Kripke,ML;Munn,CG;Jeevan,A;Tang,JM;Bucana,C
通讯作者:
Bucana,C