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CD30 as a therapeutic target in adult haematological malignancies: Where are we now?
被引:3
|作者:
Veyri, M.
[1
,4
]
Spano, J. P.
[1
]
Le Bras, F.
[2
]
Marcelin, A. G.
[3
]
Todesco, E.
[3
]
机构:
[1] Sorbonne Univ, Hop Pitie Salpetriere, AP HP, INSERM,Inst Pierre Louis Epidemiol & St Publ IPLES, Paris, France
[2] Hop Henri Mondor, AP HP, Unite Hemopathies Lymphoides, Creteil, France
[3] Sorbonne Univ, Inst Pierre Louis Epidemiol & St Publ IPLESP, INSERM, Paris, France
[4] Pitie Salpetriere, Med Oncol Dept, 47-83 Blvd Hop, F-75013 Paris, France
关键词:
brentuximab vedotin;
CAR-T cell;
CD30;
LARGE-CELL LYMPHOMA;
REFRACTORY HODGKIN LYMPHOMA;
PRIMARY EFFUSION LYMPHOMA;
HIV-INFECTED PATIENTS;
A-CHAIN IMMUNOTOXINS;
BRENTUXIMAB VEDOTIN;
SERUM-LEVELS;
IN-VITRO;
MONOCLONAL-ANTIBODIES;
PHASE-II;
D O I:
10.1111/bjh.18841
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
CD30 is a transmembrane protein from the tumour necrosis factor receptor superfamily. It is expressed on a small subset of activated T and B lymphocytes, and various lymphoid neoplasms. CD30 is a particularly interesting treatment target because its levels are high in tumours but low in healthy tissues. Several therapeutic strategies targeting CD30 have been developed, including monoclonal antibodies, conjugated antibodies (combination of brentuximab vedotin with chemotherapy or immunotherapy), bispecific antibodies and cell and gene therapies, such as anti-CD30 CAR-T cells in particular. We briefly review the biology of CD30 which makes it a good therapeutic target, and we describe all of the anti-CD30 therapies that have emerged to date.
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页码:1033 / 1046
页数:14
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