CD30 as a therapeutic target in adult haematological malignancies: Where are we now?


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
06 2023
Historique:
revised: 18 04 2023
received: 20 01 2023
accepted: 20 04 2023
medline: 6 6 2023
pubmed: 12 5 2023
entrez: 11 5 2023
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 37170397
doi: 10.1111/bjh.18841
doi:

Substances chimiques

Antibodies, Monoclonal 0
Brentuximab Vedotin 7XL5ISS668
Immunoconjugates 0
Ki-1 Antigen 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1033-1046

Informations de copyright

© 2023 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

Références

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Auteurs

M Veyri (M)

Service de Virologie, Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique (IPLESP), Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, Paris, France.

J P Spano (JP)

Service de Virologie, Sorbonne Université, INSERM, Institut Pierre Louis d'Épidémiologie et de Santé Publique (IPLESP), Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, Paris, France.

F Le Bras (F)

Unité des hémopathies lymphoïdes, Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Henri-Mondor, Créteil, France.

A G Marcelin (AG)

INSERM, Institut Pierre-Louis d'Épidémiologie et de Santé Publique (IPLESP), Sorbonne Université, Paris, France.

E Todesco (E)

INSERM, Institut Pierre-Louis d'Épidémiologie et de Santé Publique (IPLESP), Sorbonne Université, Paris, France.

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