Generation and characterization of CD1d-specific single-domain antibodies with distinct functional features

被引:17
作者
Lameris, Roeland [1 ]
de Bruin, Renee C. G. [1 ]
Henegouwen, Paul M. P. van Bergen En [2 ]
Verheul, Henk M. [1 ]
Zweegman, Sonja [3 ]
de Gruijl, Tanja D. [1 ]
van der Vliet, Hans J. [1 ]
机构
[1] Vrije Univ Amsterdam, Dept Med Oncol, Med Ctr, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[2] Univ Utrecht, Div Cell Biol, Dept Biol, Fac Sci, Utrecht, Netherlands
[3] Vrije Univ Amsterdam, Dept Haematol, Med Ctr, Amsterdam, Netherlands
关键词
cancer; CD1d; dendritic cell; invariant natural killer T-cell; variable domain of heavy-chain-only antibody; KILLER-T-CELLS; NKT CELLS; LIPID ANTIGENS; INKT CELLS; CD1D; NANOBODIES; CARCINOMA; CANCER; PHAGE; IMMUNOTHERAPY;
D O I
10.1111/imm.12635
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ligation of the CD1d antigen-presenting molecule by monoclonal antibodies (mAbs) can trigger important biological functions. For therapeutic purposes camelid-derived variable domain of heavy-chain-only antibodies (VHH) have multiple advantages over mAbs because they are small, stable and have low immunogenicity. Here, we generated 21 human CD1d-specific VHH by immunizing Lama glama and subsequent phage display. Two clones induced maturation of dendritic cells, one clone induced early apoptosis in CD1d-expressing B lymphoblasts and multiple myeloma cells, and another clone blocked recognition of glycolipid-loaded CD1d by CD1d-restricted invariant natural killer T (iNKT) cells. In contrast to reported CD1d-specific mAbs, these CD1d-specific VHH have the unique characteristic that they induce specific and well-defined biological effects. This feature, combined with the above-indicated general advantages of VHH, make the CD1d-specific VHH generated here unique and useful tools to exploit both CD1d ligation as well as disruption of CD1d-iNKT interactions in the treatment of cancer or inflammatory disorders.
引用
收藏
页码:111 / 121
页数:11
相关论文
共 47 条
[1]   Essential role of NKT cells producing IL-4 and IL-13 in the development of allergen-induced airway hyperreactivity [J].
Akbari, O ;
Stock, P ;
Meyer, E ;
Kronenberg, M ;
Sidobre, S ;
Nakayama, T ;
Taniguchi, M ;
Grusby, MJ ;
DeKruyff, RH ;
Umetsu, DT .
NATURE MEDICINE, 2003, 9 (05) :582-588
[2]   iNKT Cells Control Mouse Spontaneous Carcinoma Independently of Tumor-Specific Cytotoxic T Cells [J].
Bellone, Matteo ;
Ceccon, Monica ;
Grioni, Matteo ;
Jachetti, Elena ;
Calcinotto, Arianna ;
Napolitano, Anna ;
Freschi, Massimo ;
Casorati, Giulia ;
Dellabona, Paolo .
PLOS ONE, 2010, 5 (01)
[3]   Alternative Spliced CD1D Transcripts in Human Bronchial Epithelial Cells [J].
Benam, Kambez Hajipouran ;
Kok, Wai Ling ;
McMichael, Andrew J. ;
Ho, Ling-Pei .
PLOS ONE, 2011, 6 (08)
[4]   Invariant natural killer T cells: an innate activation scheme linked to diverse effector functions [J].
Brennan, Patrick J. ;
Brigl, Manfred ;
Brenner, Michael B. .
NATURE REVIEWS IMMUNOLOGY, 2013, 13 (02) :101-117
[5]   Role and Regulation of CD1d in Normal and Pathological B Cells [J].
Chaudhry, Mohammed S. ;
Karadimitris, Anastasios .
JOURNAL OF IMMUNOLOGY, 2014, 193 (10) :4761-4768
[6]   AN INVARIANT V-ALPHA-24-J-ALPHA-Q/V-BETA-11 T-CELL RECEPTOR IS EXPRESSED IN ALL INDIVIDUALS BY CLONALLY EXPANDED CD4-8- T-CELLS [J].
DELLABONA, P ;
PADOVAN, E ;
CASORATI, G ;
BROCKHAUS, M ;
LANZAVECCHIA, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :1171-1176
[7]   THE INHIBITORY EFFECT OF POLYMYXIN-B ON ENDOTOXIN-INDUCED ENDOGENOUS PYROGEN PRODUCTION [J].
DUFF, GW ;
ATKINS, E .
JOURNAL OF IMMUNOLOGICAL METHODS, 1982, 52 (03) :333-340
[8]   Requirements for CD1d recognition by human invariant V alpha 24(+) CD4(-)CD8(-) T cells [J].
Exley, M ;
Garcia, J ;
Balk, SP ;
Porcelli, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :109-120
[9]   Opinion - NKT cells: what's in a name? [J].
Godfrey, DI ;
MacDonald, HR ;
Kronenberg, M ;
Smyth, MJ ;
Van Kaer, L .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (03) :231-237
[10]   Going both ways: immune regulation via CD1d-dependent NKT cells [J].
Godfrey, DI ;
Kronenberg, M .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (10) :1379-1388