Expression of CD6 in Aggressive NK/T-cell Neoplasms and Assessment as a Potential Therapeutic Target: A Bone Marrow Pathology Group Study.

ANKL model Aggressive NK-Cell Leukemia/Lymphoma (ANKLL) CD6 CD6-ADC Extranodal NK/T-cell lymphoma (ENKTL)

Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
08 Jul 2024
Historique:
received: 24 05 2024
revised: 25 06 2024
accepted: 30 06 2024
medline: 2 8 2024
pubmed: 2 8 2024
entrez: 1 8 2024
Statut: aheadofprint

Résumé

Aggressive NK/T-Cell neoplasms are rare hematological malignancies characterized by the abnormal proliferation of NK or NK-like T (NK/T) cells. CD6 is a transmembrane signal transducing receptor involved in lymphocyte activation and differentiation. This study aimed to investigate the CD6 expression in these malignancies and explore the potential of targeting CD6 in these diseases. We conducted a retrospective study with totally 41 cases to investigate the expression of CD6 by immunohistochemistry, including aggressive NK-cell leukemia/lymphoma (ANKLL: N = 10) and extranodal NK/T-cell lymphoma (ENKTL: N = 31). A novel ANKLL model was applied for proof-of-concept functional studies of a CD6 antibody-drug-conjugate (CD6-ADC) both in vitro and in animal trial. CD6 was expressed in 68.3% (28/41) of cases (70% (7/10) of ANKLL and 67.7% (21/31) of ENKTL). The median overall survival (OS) for ANKLL and ENTKL cases was 1 and 12 months, respectively, with no significant difference in OS based on CD6 expression (p > 0.05, Kaplan-Meier with log-rank test). In vitro exposure of the CCANKL cell line, derived from an ANKL patient, to an anti-CD6ADC resulted in dose dependent induction of apoptosis. Furthermore, CCANKL engraftment in NSG mice could be blocked by treatment with the anti-CD6 ADC. To date, this is the first report to explore the expression of CD6 in ANKLL and ENKTL and confirms its expression in the majority of cases. The in vitro and in vivo data support further investigation of CD6 as a potential therapeutic target in these aggressive NK/T-cell malignancies.

Sections du résumé

BACKGROUND BACKGROUND
Aggressive NK/T-Cell neoplasms are rare hematological malignancies characterized by the abnormal proliferation of NK or NK-like T (NK/T) cells. CD6 is a transmembrane signal transducing receptor involved in lymphocyte activation and differentiation. This study aimed to investigate the CD6 expression in these malignancies and explore the potential of targeting CD6 in these diseases.
MATERIALS AND METHODS METHODS
We conducted a retrospective study with totally 41 cases to investigate the expression of CD6 by immunohistochemistry, including aggressive NK-cell leukemia/lymphoma (ANKLL: N = 10) and extranodal NK/T-cell lymphoma (ENKTL: N = 31). A novel ANKLL model was applied for proof-of-concept functional studies of a CD6 antibody-drug-conjugate (CD6-ADC) both in vitro and in animal trial.
RESULTS RESULTS
CD6 was expressed in 68.3% (28/41) of cases (70% (7/10) of ANKLL and 67.7% (21/31) of ENKTL). The median overall survival (OS) for ANKLL and ENTKL cases was 1 and 12 months, respectively, with no significant difference in OS based on CD6 expression (p > 0.05, Kaplan-Meier with log-rank test). In vitro exposure of the CCANKL cell line, derived from an ANKL patient, to an anti-CD6ADC resulted in dose dependent induction of apoptosis. Furthermore, CCANKL engraftment in NSG mice could be blocked by treatment with the anti-CD6 ADC.
CONCLUSION CONCLUSIONS
To date, this is the first report to explore the expression of CD6 in ANKLL and ENKTL and confirms its expression in the majority of cases. The in vitro and in vivo data support further investigation of CD6 as a potential therapeutic target in these aggressive NK/T-cell malignancies.

Identifiants

pubmed: 39089930
pii: S2152-2650(24)00247-7
doi: 10.1016/j.clml.2024.06.013
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure EH: Abcon Therapeutics, Avalere Health, Novartis, Eli Lilly. FL: Abcon Therapeutics.

Auteurs

Xiaoxian Zhao (X)

Department of Pathology, Wake Forest University School of Medicine, Winston Salem, NC; Department of Laboratory Medicine, Cleveland Clinic, Cleveland OH.

Chad M McCall (CM)

Carolinas Pathology Group, Charlotte, NC.

Jared G Block (JG)

Carolinas Pathology Group, Charlotte, NC.

Sarah L Ondrejka (SL)

Department of Laboratory Medicine, Cleveland Clinic, Cleveland OH.

Beenu Thakral (B)

Department of Hematopathology, MD Anderson Cancer Center, Houston, TX.

Sa A Wang (SA)

Department of Hematopathology, MD Anderson Cancer Center, Houston, TX.

Yahya Al-Ghamdi (Y)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York City, NY.

Wayne Tam (W)

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York City, NY.

Brittany Coffman (B)

Department of Pathology, University of New Mexico, Albuquerque, NM.

Kathryn Foucar (K)

Department of Pathology, University of New Mexico, Albuquerque, NM.

Parnaz Daneshpajouhnejad (P)

Department of Pathology, University of Pennsylvania, Philadelphia, PA.

Adam Bagg (A)

Department of Pathology, University of Pennsylvania, Philadelphia, PA.

Feng Lin (F)

Department of Inflammation & Immunity, Cleveland Clinic, Cleveland OH.

Eric D Hsi (ED)

Department of Pathology, Wake Forest University School of Medicine, Winston Salem, NC; Department of Laboratory Medicine, Cleveland Clinic, Cleveland OH; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN. Electronic address: Hsi.Eric@mayo.edu.

Classifications MeSH