Evolving Roles for Targeting CTLA-4 in Cancer Immunotherapy

被引:140
作者
Zhao, Yinghao [1 ]
Yang, Wei [1 ]
Huang, Yuanyuan [2 ]
Cui, Ranji [1 ]
Li, Xiangyan [3 ]
Li, Bingjin [1 ]
机构
[1] Jilin Univ, Hosp 2, Jilin Prov Key Lab Mol & Chem Genet, Changchun, Jilin, Peoples R China
[2] Jilin Univ, Hosp 1, Dept Pediat, Changchun, Jilin, Peoples R China
[3] Changchun Univ Chinese Med, Affiliated Hosp, Jilin Prov Key Lab BioMacromol Chinese Med, Jilin Ginseng Acad, Changchun, Jilin, Peoples R China
关键词
Ctla-4; PD-1; Antibody; ipilimumab; Tremelimumab; CELL LUNG-CANCER; RESISTANT PROSTATE-CANCER; T-CELLS; ADVERSE EVENTS; RS231775; POLYMORPHISM; ANTI-CTLA-4; ANTIBODY; DOUBLE-BLIND; HEPATOCELLULAR-CARCINOMA; LYMPHOCYTE MOLECULES; BIOLOGICAL FUNCTION;
D O I
10.1159/000490025
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is a membrane glycoprotein expressed by activated effector T cells (Teffs) and participates in the repression of T cell proliferation, cell cycle progression and cytokine production. Currently, antibodies targeting CTLA-4, ipilimumab and tremelimumab are widely used as a therapeutic approach in a variety of human malignancies. However, their detailed mechanism remains unclear. Therefore, in this review, we focused specifically on recent findings concerning the role of CTLA-4 in immune response and also discussed clinical studies of targeting CTLA-4, alone or in combination with other therapies for the treatment of cancers. CTLA-4 blockade is used as a therapeutic approach for the treatment of cancer through competing with CD28-positive costimulation for binding to their shared B7 ligands or exhibiting direct inhibitory effect on signaling molecules in the cytoplasmic tail. At present, antibodies for targeting CTLA-4 or in combination with other therapies significantly reinforced the anti-tumor effect and improved the prognosis of malignant disease. In addition, severe adverse events of targeting CTLA-4 therapy could be a challenge for the development of this therapeutic strategy. This review may provide some new insights for clinical studies of targeting CTLA-4. (c) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:721 / 734
页数:14
相关论文
共 126 条
[61]   Enhancement of antitumor immunity by CTLA-4 blockade [J].
Leach, DR ;
Krummel, MF ;
Allison, JP .
SCIENCE, 1996, 271 (5256) :1734-1736
[62]   Molecular basis of T cell inactivation by CTLA-4 [J].
Lee, KM ;
Chuang, E ;
Griffin, M ;
Khattri, R ;
Hong, DK ;
Zhang, WG ;
Straus, D ;
Samelson, LE ;
Thompson, CB ;
Bluestone, JA .
SCIENCE, 1998, 282 (5397) :2263-2266
[63]   A meta-analysis of the association between CTLA-4+49 A/G,-318 C/T, and IL-1 polymorphisms and susceptibility to cervical cancer [J].
Lee, Y. H. ;
Song, G. G. .
NEOPLASMA, 2014, 61 (04) :481-490
[64]   Association of CTLA-4 gene polymorphisms with sporadic breast cancer risk and clinical features in Han women of Northeast China [J].
Li, Dalin ;
Zhang, Qiujin ;
Xu, Fengyan ;
Fu, Zhenkun ;
Yuan, Weiguang ;
Li, Dianjun ;
Pang, Da .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2012, 364 (1-2) :283-290
[65]   Cutting edge:: Cbl-b:: One of the key molecules tuning CD28- and CTLA-4-Mediated T cell costimulation [J].
Li, DD ;
Gál, I ;
Vermes, C ;
Alegre, ML ;
Chong, ASF ;
Chen, LP ;
Shao, Q ;
Adarichev, V ;
Xu, XM ;
Koreny, T ;
Mikecz, K ;
Finnegan, A ;
Glant, TT ;
Zhang, J .
JOURNAL OF IMMUNOLOGY, 2004, 173 (12) :7135-7139
[66]   Combined OX40 ligation plus CTLA-4 blockade More than the sum of its parts [J].
Linch, Stefanie N. ;
Redmond, William L. .
ONCOIMMUNOLOGY, 2014, 3 (03)
[67]  
LINDSTEN T, 1993, J IMMUNOL, V151, P3489
[68]   HUMAN B7-1 (CD80) AND B7-2 (CD86) BIND WITH SIMILAR AVIDITIES BUT DISTINCT KINETICS TO CD28 AND CTLA-4 RECEPTORS [J].
LINSLEY, PS ;
GREENE, JL ;
BRADY, W ;
BAJORATH, J ;
LEDBETTER, JA ;
PEACH, R .
IMMUNITY, 1994, 1 (09) :793-801
[69]   CTLA-4 IS A 2ND RECEPTOR FOR THE B-CELL ACTIVATION ANTIGEN-B7 [J].
LINSLEY, PS ;
BRADY, W ;
URNES, M ;
GROSMAIRE, LS ;
DAMLE, NK ;
LEDBETTER, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 174 (03) :561-569
[70]   COEXPRESSION AND FUNCTIONAL COOPERATION OF CTLA-4 AND CD28 ON ACTIVATED LYMPHOCYTES-T [J].
LINSLEY, PS ;
GREENE, JL ;
TAN, P ;
BRADSHAW, J ;
LEDBETTER, JA ;
ANASETTI, C ;
DAMLE, NK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1595-1604