Intraocular tumor antigen drains specifically to submandibular lymph nodes, resulting in an abortive cytotoxic T cell reaction

被引:26
作者
Boonman, ZFHM
van Mierlo, GJD
Fransen, MF
Franken, KLMC
Offringa, R
Melief, CJM
Jager, MJ
Toes, REM
机构
[1] Leiden Univ, Med Ctr, Dept Ophthalmol, NL-2300 RC Leiden, Netherlands
[2] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Tranfus, NL-2300 RC Leiden, Netherlands
[3] Leiden Univ, Med Ctr, Dept Rheumatol, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.4049/jimmunol.172.3.1567
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ocular immune privilege is considered essential in the protection against sight-threatening immune responses, as illustrated by the ability of the ocular environment to permit the growth of tumors that are rejected when implanted at other sites. Although several studies indicate that soluble Ag can drain directly into the spleen when injected into the anterior chamber, the primary site of intraocular tumor Ag presentation to tumor-specific CTLs has not been studied. To gain a better understanding of the mechanism involved in ocular immune privilege, we examined to which lymphoid organs anterior chamber tumor Ags primarily drain. Our data show that intraocular tumor Ag drains exclusively to the submandibular lymph nodes, resulting in activation of tumor-specific CTLs, whereas no Ag drainage was found in spleen. However, these tumor-specific CTLs do not distribute systemically and, as a consequence, intraocular tumor growth is unhampered. A similar lack of CTL efficacy has been observed in mice bearing s.c. tumors, which is converted to a systemic tumoricidal CTL response by administration of agonistic anti-CD40 mAb. In contrast, systemic anti-CD40 treatment of eye tumor-bearing mice did not result in mobilizing tumor-specific CTLs or tumor eradication. Together, these results show that intraocular tumor Ag drains to regional lymph nodes for activation of tumor-specific CTLs. However, the induced tumor-specific immunity is insufficient for tumor clearance, even combined with otherwise highly effective immune intervention protocols.
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页码:1567 / 1574
页数:8
相关论文
共 53 条
[11]   MIP-2 recruits NKT cells to the spleen during tolerance induction [J].
Faunce, DE ;
Sonoda, KH ;
Stein-Streilein, J .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :313-321
[12]   Purification of His-tagged proteins by immobilized chelate affinity chromatography: The benefits from the use of organic solvent [J].
Franken, KLMC ;
Hiemstra, HS ;
van Meijgaarden, KE ;
Subronto, Y ;
den Hartigh, J ;
Ottenhoff, THM ;
Drijfhout, JW .
PROTEIN EXPRESSION AND PURIFICATION, 2000, 18 (01) :95-99
[13]   Human dendritic cells activated by TSLP and CD40L induce proallergic cytotoxic T cells [J].
Gilliet, M ;
Soumelis, V ;
Watanabe, N ;
Hanabuchi, S ;
Antonenko, S ;
de Waal-Malefyt, R ;
Liu, YJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (08) :1059-1063
[14]  
Gong HY, 1996, MICROSC RES TECHNIQ, V33, P336, DOI 10.1002/(SICI)1097-0029(19960301)33:4<336::AID-JEMT4>3.0.CO
[15]  
2-N
[16]  
GREEN K, 1977, T OPHTHAL SOC UK, V97, P731
[17]   FAS LIGAND-INDUCED APOPTOSIS AS A MECHANISM OF IMMUNE PRIVILEGE [J].
GRIFFITH, TS ;
BRUNNER, T ;
FLETCHER, SM ;
GREEN, DR ;
FERGUSON, TA .
SCIENCE, 1995, 270 (5239) :1189-1192
[18]   Induction of interleukin 10-producing, nonproliferating CD4+ T cells with regulatory properties by repetitive stimulation with allogeneic immature human dendritic cells [J].
Jonuleit, H ;
Schmitt, E ;
Schuler, G ;
Knop, J ;
Enk, AH .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (09) :1213-1222
[19]   Dendritic cells as a tool to induce anergic and regulatory T cells [J].
Jonuleit, H ;
Schmitt, E ;
Steinbrink, K ;
Enk, AH .
TRENDS IN IMMUNOLOGY, 2001, 22 (07) :394-400
[20]   Memory CD8+ T cell differentiation:: initial antigen encounter triggers a developmental program in naive cells [J].
Kaech, SM ;
Ahmed, R .
NATURE IMMUNOLOGY, 2001, 2 (05) :415-422