CD30: an important new target in hematologic malignancies

被引:59
|
作者
Deutsch, Yehuda E. [1 ,2 ]
Tadmor, Tamar [3 ]
Podack, Eckhard R. [4 ]
Rosenblatt, Joseph D. [1 ,2 ,4 ]
机构
[1] Univ Miami, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Med, Div Hematol Oncol, Miami, FL 33136 USA
[3] Bnai Zion Med Ctr, Hematol Oncol Unit, Haifa, Israel
[4] Univ Miami, Miller Sch Med, Dept Microbiol & Immunol, Miami, FL 33136 USA
关键词
Lymphoma and Hodgkin disease; antibody-based immunotherapy; CD30; brentuximab vedotin; LARGE-CELL LYMPHOMA; ANTI-CD30; ANTIBODY; 5F11; REED-STERNBERG CELLS; FACTOR-KAPPA-B; REFRACTORY HODGKINS-DISEASE; RETRACTED ARTICLE. SEE; HIGH SERUM-LEVEL; CD4(+) T-CELLS; SOLUBLE CD30; ANTITUMOR-ACTIVITY;
D O I
10.3109/10428194.2011.574761
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD30 is abundantly and selectively expressed on the surface of Hodgkin Reed-Sternberg cells, anaplastic large cell lymphomas (ALCLs), and other lymphoid malignancies as well as on several non-lymphoid malignancies including selected germ cell tumors. Expression of CD30 on normal cells is highly restricted, thereby allowing differential targeting of malignant cells. CD30, a member of the tumor necrosis factor (TNF)-receptor family has pleiotropic biologic functions, and antibodies targeting CD30 and other TNF family receptors can exhibit both agonistic and antagonistic signaling functions. Recently, antibody-drug conjugates targeting CD30, such as brentuximab vedotin, have shown striking activity in phase I and II trials, with manageable toxicity. This has defined an important emerging role for targeting of CD30 in the setting of Hodgkin lymphoma, ALCL, and possibly other CD30+ malignancies.
引用
收藏
页码:1641 / 1654
页数:14
相关论文
共 50 条
  • [41] CD30 in Systemic Mastocytosis
    van Anrooij, Bjorn
    Kluin, Philip M.
    Elberink, Joanne N. G. Oude
    Kluin-Nelemans, Johanna C.
    IMMUNOLOGY AND ALLERGY CLINICS OF NORTH AMERICA, 2014, 34 (02) : 341 - +
  • [42] Ras as a therapeutic target in hematologic malignancies
    Alvarado, Yesid
    Giles, Francis J.
    EXPERT OPINION ON EMERGING DRUGS, 2007, 12 (02) : 271 - 284
  • [43] CD200, A CELL SURFACE PROTEIN WITH IMMUNOREGULATORY FUNCTION, IS A NEW POTENTIAL TARGET FOR HEMATOLOGIC MALIGNANCIES IMMUNOTHERAPY
    Brunetti, L.
    Abate, E.
    Gorrese, M.
    Raia, M.
    Pascariello, C.
    Gravetti, A.
    Scalia, G.
    Del Vecchio, L.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 : 72 - 72
  • [44] Biology and Expression of CD30
    Sotomayor, Eduardo M.
    CLINICAL ADVANCES IN HEMATOLOGY & ONCOLOGY, 2014, 12 (04) : 3 - 8
  • [45] CD30/CD30 ligand and CD40/CD40 ligand in malignant lymphoid disorders
    Younes, A
    Carbone, A
    INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 1999, 14 (03): : 135 - 143
  • [46] A critical role of CD30 ligand/CD30 in controlling inflammatory bowel diseases in mice
    Sun, Xun
    Somada, Shinichi
    Shibata, Kensuke
    Muta, Hiromi
    Yamada, Hisakata
    Yoshihara, Hirofumi
    Honda, Kuniomi
    Nakamura, Kazuhiko
    Takayanagi, Ryhoichi
    Tani, Kenzaburo
    Podack, Eckhard R.
    Yoshikai, Yasunobu
    GASTROENTEROLOGY, 2008, 134 (02) : 447 - 458
  • [47] Soluble CD30 Level and CD30 Promoter Microsatellite Length Polymorphism in Renal Transplantation
    Oh, S. H.
    Kim, Y. H.
    Kang, S. W.
    Kim, T. H.
    Park, S. J.
    Kang, M. S.
    Yoon, Y. C.
    Kim, Y. W.
    TRANSPLANTATION, 2012, 94 (10) : 584 - 584
  • [48] Soluble CD30 binds to CD153 with high affinity and blocks transmembrane signaling by CD30
    Hargreaves, PG
    Al-Shamkhani, A
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2002, 32 (01) : 163 - 173
  • [49] Use of CD30 expression in human malignant mesothelioma as a novel therapeutic target
    Dowlati, Afshin
    Dabir, Snehal
    Kresak, Adam
    Yang, Michael
    Wildey, Gary
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (15)
  • [50] Expression of CD30 Antigen in Human Malignant Mesotheliomas: A Potential Therapeutic Target
    Sethi, A.
    Sheibani, K.
    Vasef, M. A.
    LABORATORY INVESTIGATION, 2014, 94 : 494A - 494A