Mechanism of Action of IL-7 and Its Potential Applications and Limitations in Cancer Immunotherapy

被引:89
作者
Gao, Jianbao [1 ]
Zhao, Lintao [1 ]
Wan, Yisong Y. [2 ]
Zhu, Bo [1 ,3 ]
机构
[1] Third Mil Med Univ, Inst Canc, Xinqiao Hosp, Chongqing 400037, Peoples R China
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[3] Third Mil Med Univ, Biomed Anal Ctr, Chongqing 400038, Peoples R China
关键词
IL-7; cancer; immunotherapy; T-CELL HOMEOSTASIS; INTERLEUKIN-7 RECEPTOR EXPRESSION; ACUTE LYMPHOBLASTIC-LEUKEMIA; ANTITUMOR-ACTIVITY; PROSTATE-CANCER; GENE-EXPRESSION; CD8(+); NAIVE; PROLIFERATION; RECOMBINANT;
D O I
10.3390/ijms160510267
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-7 (IL-7) is a non-hematopoietic cell-derived cytokine with a central role in the adaptive immune system. It promotes lymphocyte development in the thymus and maintains survival of naive and memory T cell homeostasis in the periphery. Moreover, it is important for the organogenesis of lymph nodes (LN) and for the maintenance of activated T cells recruited into the secondary lymphoid organs (SLOs). The immune capacity of cancer patients is suppressed that is characterized by lower T cell counts, less effector immune cells infiltration, higher levels of exhausted effector cells and higher levels of immunosuppressive cytokines, such as transforming growth factor (TGF-). Recombinant human IL-7 (rhIL-7) is an ideal solution for the immune reconstitution of lymphopenia patients by promoting peripheral T cell expansion. Furthermore, it can antagonize the immunosuppressive network. In animal models, IL-7 has been proven to prolong the survival of tumor-bearing hosts. In this review, we will focus on the mechanism of action and applications of IL-7 in cancer immunotherapy and the potential restrictions for its usage.
引用
收藏
页码:10267 / 10280
页数:14
相关论文
共 79 条
[1]  
Al-Rawi MAA, 2003, HISTOL HISTOPATHOL, V18, P911, DOI 10.14670/HH-18.911
[2]   Role of CXCR3 Ligands in IL-7/IL-7Rα-Fc-Mediated Antitumor Activity in Lung Cancer [J].
Andersson, Asa ;
Srivastava, Minu K. ;
Harris-White, Marni ;
Huang, Min ;
Zhu, Li ;
Elashoff, David ;
Strieter, Robert M. ;
Dubinett, Steven M. ;
Sharma, Sherven .
CLINICAL CANCER RESEARCH, 2011, 17 (11) :3660-3672
[3]   IL-7 Promotes CXCR3 Ligand-Dependent T Cell Antitumor Reactivity in Lung Cancer [J].
Andersson, Asa ;
Yang, Seok-Chul ;
Huang, Min ;
Zhu, Li ;
Kar, Upendra K. ;
Batra, Rai K. ;
Elashoff, David ;
Strieter, Robert M. ;
Dubinett, Steven M. ;
Sharma, Sherven .
JOURNAL OF IMMUNOLOGY, 2009, 182 (11) :6951-6958
[4]  
Anne L., 2011, TRENDS IMMUNOL, V32, P6, DOI [10.1016/j.it.2010.10.00421123113, DOI 10.1016/J.IT.2010.10.004]
[5]   Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes [J].
Bajenoff, Marc ;
Egen, Jackson G. ;
Koo, Lily Y. ;
Laugier, Jean Pierre ;
Brau, Frederic ;
Glaichenhaus, Nicolas ;
Germain, Ronald N. .
IMMUNITY, 2006, 25 (06) :989-1001
[6]   Interleukin-7 in T-cell acute lymphoblastic leukemia: An extrinsic factor supporting leukemogenesis? [J].
Barata, JT ;
Cardoso, AA ;
Boussiotis, VA .
LEUKEMIA & LYMPHOMA, 2005, 46 (04) :483-495
[7]   Activation of PI3K is indispensable for interleukin 7-mediated viability, proliferation, glucose use, and growth of T cell acute lymphoblastic leukemia cells [J].
Barata, JT ;
Silva, A ;
Brandao, JG ;
Nadler, LM ;
Cardoso, AA ;
Boussiotis, VA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (05) :659-669
[8]   Injection of glycosylated recombinant simian IL-7 provokes rapid and massive T-cell homing in rhesus macaques [J].
Beq, Stephanie ;
Rozlan, Sandra ;
Gautier, David ;
Parker, Raphaelle ;
Mersseman, Veronique ;
Schilte, Clementine ;
Assouline, Brigitte ;
Rance, Iann ;
Lavedan, Pascal ;
Morre, Michel ;
Cheynier, Remi .
BLOOD, 2009, 114 (04) :816-825
[9]   Serum levels of IL-7 in bone marrow transplant recipients: relationship to clinical characteristics and lymphocyte count [J].
Bolotin, E ;
Annett, G ;
Parkman, R ;
Weinberg, K .
BONE MARROW TRANSPLANTATION, 1999, 23 (08) :783-788
[10]   A distal region in the interferon-γ gene is a site of epigenetic remodeling and transcriptional regulation by interleukin-2 [J].
Bream, JH ;
Hodge, DL ;
Gonsky, R ;
Spolski, R ;
Leonard, WJ ;
Krebs, S ;
Targan, S ;
Morinobu, A ;
O'Shea, JJ ;
Young, HA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :41249-41257