Early local generation of C5a initiates the elicitation of contact sensitivity by leading to early T cell recruitment

被引:98
作者
Tsuji, RF
Kawikova, I
Ramabhadran, R
Akahira-Azuma, M
Taub, D
Hugli, TE
Gerard, C
Askenase, PW
机构
[1] Noda Inst Sci Res, Noda, Chiba 2780037, Japan
[2] Yale Univ, Sch Med, Dept Internal Med, Allergy & Clin Immunol Sect, New Haven, CT 06520 USA
[3] NIA, Clin Immunol Sect, NIH, Geriatr Res Ctr, Baltimore, MD 21224 USA
[4] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[5] Harvard Univ, Sch Med, Childrens Hosp, Perlmutter Lab, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.165.3.1588
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have shown previously that an early complement C5-dependent cascade is required to recruit T cells to elicit 24-h contact sensitivity (CS) responses. In this paper, we have characterized molecular events of this early required cascade by biochemically analyzing extracts of mouse ears undergoing elicitation of CS, Chemotactic activity was found after local Ag challenge, in CS ear extracts early (by 1 h), in CS ear extracts late (through 24 h), in previously immunized mice, but not in ears of vehicle-immunized or non-immune challenged mice. The early chemotactic activity at 2 h was likely caused by C5a, because it was neutralized in vitro. by anti-C5a Ab, was inactive on C5aR-deficient (C5aR(-/-)) macrophages, and was absent In C5-deficient mice. The activity was present in T cell-deficient mice, but elaboration was Ag-specific. This T cell-independent, Ag specific elaboration of C5a early in CS ear responses likely led to T cell recruitment, because subsequent local IFN-gamma mRNA and protein expression, as markers of T cell arrival and activation, began by 4 h after Ag challenge. In contrast to early C5a chemotactic activity, late chemotactic activity 24 h after Ag challenge was unaffected by anti-C5, was active on C5aR(-/-) macrophages, was T cell-dependent, and by ELISA appeared largely due to chemokines (macrophage-inflammatory protein-1 alpha and 1 beta, IFN-gamma-inducible protein-10, and monocyte chemoattractant protein-1). Importantly, early generation of C5a was required for T cell recruitment because C5aR(-/-) mice had absent 24-h CS, Taken together, these findings indicate an important linkage of C5a as a component of early activated innate immunity that is required for later elicitation of acquired T cell immunity, probably by facilitating the initial recruitment of T cells into the Ag-challenged local site in CS responses.
引用
收藏
页码:1588 / 1598
页数:11
相关论文
共 47 条
[1]   Interferon-gamma inducible protein (IP-10) expression is mediated by CD8(+) T cells and is regulated by CD4(+) T cells during the elicitation of contact of hypersensitivity [J].
Abe, M ;
Kondo, T ;
Xu, H ;
Fairchild, RL .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (03) :360-366
[2]  
Askenase P W., 1998, Allergy. Principles Practice. St.Louis, P323
[3]   T-CELL-DEPENDENT MAST-CELL DE-GRANULATION AND RELEASE OF SEROTONIN IN MURINE DELAYED-TYPE HYPERSENSITIVITY [J].
ASKENASE, PW ;
BURSZTAJN, S ;
GERSHON, MD ;
GERSHON, RK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 152 (05) :1358-1374
[4]  
ASKENASE PW, 1974, IMMUNOLOGY, V27, P563
[5]   Chemokines and leukocyte traffic [J].
Baggiolini, M .
NATURE, 1998, 392 (6676) :565-568
[6]   ANAPHYLATOXIN INACTIVATOR OF HUMAN PLASMA - ITS ISOLATION AND CHARACTERIZATION AS A CARBOXYPEPTIDASE [J].
BOKISCH, VA ;
MULLEREB.HJ .
JOURNAL OF CLINICAL INVESTIGATION, 1970, 49 (12) :2427-&
[7]   MAJOR HISTOCOMPATIBILITY COMPLEX CLASS I-RESTRICTED CD8(+) T-CELLS AND CLASS II-RESTRICTED CD4(+) T-CELLS, RESPECTIVELY, MEDIATE AND REGULATE CONTACT SENSITIVITY TO DINITROFLUOROBENZENE [J].
BOUR, H ;
PEYRON, E ;
GAUCHERAND, M ;
GARRIGUE, JL ;
DESVIGNES, C ;
KAISERLIAN, D ;
REVILLARD, JP ;
NICOLAS, JF .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (11) :3006-3010
[8]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[9]   C3d of complement as a molecular adjuvant: Bridging innate and acquired immunity [J].
Dempsey, PW ;
Allison, MED ;
Akkaraju, S ;
Goodnow, CC ;
Fearon, DT .
SCIENCE, 1996, 271 (5247) :348-350
[10]   Elements of immunity - The instructive role of innate immunity in the acquired immune response [J].
Fearon, DT ;
Locksley, RM .
SCIENCE, 1996, 272 (5258) :50-54