Paclitaxel and immune system

被引:144
作者
Javeed, Aqeel [3 ]
Ashraf, Muhammad [3 ]
Riaz, Amjad [2 ]
Ghafoor, Aamir [4 ]
Afzal, Sheryar [3 ]
Mukhtar, Muhammad Mahmood [1 ]
机构
[1] Univ Vet & Anim Sci, Dept Microbiol, Lahore 54600, Punjab, Pakistan
[2] Univ Vet & Anim Sci, Dept Theriogenol, Lahore 54600, Punjab, Pakistan
[3] Univ Vet & Anim Sci, Dept Pharmacol & Toxicol, Lahore 54600, Punjab, Pakistan
[4] Massey Univ, Inst Mol Biosci, Palmerston North, New Zealand
关键词
Paclitaxel; Tumor; Immune; Autoimmune disorders; Transplantation; REGULATORY T-CELLS; COLLAGEN-INDUCED ARTHRITIS; BREAST-CARCINOMA CELLS; NATURAL-KILLER-CELLS; NF-KAPPA-B; NITRIC-OXIDE SYNTHASE; OVARIAN-CANCER CELLS; MURINE MACROPHAGES; TUMOR-IMMUNITY; LUNG-CANCER;
D O I
10.1016/j.ejps.2009.08.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemotherapy remains the mainstay of treatment for both early stage as well as metastatic tumors. Paclitaxel (PTX), a novel anticancer drug, is a prominent taxane which is active against a broad range of tumors that are generally considered to be refractory to conventional chemotherapy, with benefits gained ill terms of overall survival and disease-free survival. PTX is initially characterized as a mitotic inhibitor, and its anti-neoplastic effect is derived from binding to tubulin and excessive microtube stabilization. Interestingly, drugs traditionally used for tumor cytoreduction, call exert both positive and negative effects on the host's immune system. PTX also exerts effects on the immune system and displays immunomodulatory traits. For example, PTX is immunostimulatory against tumors and also regulates lymphocyte activation suggesting that apart from promoting inhibition in cell division, it also has some other features and mechanisms which need to be taken into account. The present article reviews the clinical and experimental findings with regard to the effects of PTX on the immune cells including macrophages, dendritic cells (DCs), natural killer (NK) cells, and T and B lymphocytes together with its clinical applications in autoimmune disorders and organ trans plantation which reflect greater therapeutic application of PTX beyond tumor chemotherapy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:283 / 290
页数:8
相关论文
共 107 条
[1]  
Abbara Chadi, 2004, Drug Metabolism and Drug Interactions, V20, P219
[2]   Immune responses to p53 in patients with cancer:enrichment in tetramer+p53 peptide-specific T cells and regulatory T cells at tumor sites [J].
Albers, AE ;
Ferris, RL ;
Kim, GG ;
Chikamatsu, K ;
DeLeo, AB ;
Whiteside, TL .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2005, 54 (11) :1072-1081
[3]  
Amato SF, 1998, CANCER RES, V58, P241
[4]   Taxol involution of collagen-induced arthritis:: Ultrastructural correlation with the inhibition of synovitis and neovascularization [J].
Arsenault, AL ;
Lhoták, S ;
Hunter, WL ;
Banquerigo, MLC ;
Brahn, E .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 86 (03) :280-289
[5]  
Arsenault AL, 2000, J RHEUMATOL, V27, P582
[6]   A phase 1 study of pralatrexate in combination with paclitaxel or docetaxel in patients with advanced solid tumors [J].
Azzoli, Christopher G. ;
Krug, Lee M. ;
Gomez, Jorge ;
Miller, Vincent A. ;
Kris, Mark G. ;
Ginsberg, Michelle S. ;
Henry, Roxanne ;
Jones, Jessica ;
Tyson, Leslie ;
Dunne, Megan ;
Pizzo, Barbara ;
Farmer, Amy ;
Venkatraman, Ennapadam ;
Steffen, Robert ;
Sirotnak, F. M. .
CLINICAL CANCER RESEARCH, 2007, 13 (09) :2692-2698
[7]  
Bhan V, 2004, ONCOL REP, V11, P893
[8]   REGRESSION OF COLLAGEN-INDUCED ARTHRITIS WITH TAXOL, A MICROTUBULE STABILIZER [J].
BRAHN, E ;
TANG, C ;
BANQUERIGO, ML .
ARTHRITIS AND RHEUMATISM, 1994, 37 (06) :839-845
[9]  
Byrd-Leifer CA, 2001, EUR J IMMUNOL, V31, P2448, DOI 10.1002/1521-4141(200108)31:8<2448::AID-IMMU2448>3.0.CO
[10]  
2-N