KIR3DL2 contributes to the typing of acute adult T-cell leukemia and is a potential therapeutic target

Adult T-cell leukemia (ATL) is a lymphoid neoplasm caused by human T-cell leukemia virus type 1 (HTLV-1), which encodes the transcriptional activator Tax, which participates in the immortalization of infected T cells. ATL is classified into 4 subtypes: smoldering, chronic, acute, and lymphoma. We de...

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Veröffentlicht in:Blood 2022-09, Vol.140 (13), p.1522-1532
Hauptverfasser: Cheminant, Morgane, Lhermitte, Ludovic, Bruneau, Julie, Sicard, Hélène, Bonnafous, Cécile, Touzart, Aurore, Bourbon, Estelle, Ortonne, Nicolas, Genestier, Laurent, Gaulard, Philippe, Palmic, Patricia, Suarez, Felipe, Frenzel, Laurent, Naveau, Louise, Bazarbachi, Ali, Dussiot, Mickaël, Waast, Laetitia, Avettand-Fenoel, Véronique, Brouzes, Chantal, Pique, Claudine, Lepelletier, Yves, Asnafi, Vahid, Marçais, Ambroise, Hermine, Olivier
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Sprache:eng
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Zusammenfassung:Adult T-cell leukemia (ATL) is a lymphoid neoplasm caused by human T-cell leukemia virus type 1 (HTLV-1), which encodes the transcriptional activator Tax, which participates in the immortalization of infected T cells. ATL is classified into 4 subtypes: smoldering, chronic, acute, and lymphoma. We determined whether natural killer receptors (NKRs) were expressed in ATL. NKR expression (KIR2DL1/2DS1, KIR2DL2/2DL3/2DS2, KIR3DL2, NKG2A, NKG2C, and NKp46) was assessed in a discovery cohort of 21 ATL, and KIR3DL2 was then assessed in 71 patients with ATL. KIR3DL2 was the only NKR among those studied frequently expressed by acute-type vs lymphoma- and chronic/smoldering-type ATL (36 of 40, 4 of 16, and 1 of 15, respectively; P = .001), although acute- and lymphoma-type ATL had similar mutation profiles by targeted exome sequencing. The correlation of KIR3DL2 expression with promoter demethylation was determined by microarray-based DNA methylation profiling. To explore the role of HTLV-1, KIR3DL2 and TAX messenger RNA (mRNA) expression levels were assessed by PrimeFlow RNA in primary ATL and in CD4+ T cells infected with HTLV-1 in vitro. TAX mRNA and KIR3DL2 protein expressions were correlated on ATL cells. HTLV-1 infection triggered KIR3DL2 by CD4+ cells but Tax alone did not induce KIR3DL2 expression. Ex vivo, autologous, antibody-dependent cell cytotoxicity using lacutamab, a first-in-class anti-KIR3DL2 humanized antibody, selectively killed KIR3DL2+ primary ATL cells ex vivo. To conclude, KIR3DL2 expression is associated with acute-type ATL. Transcription of KIR3DL2 may be triggered by HTLV-1 infection and correlates with hypomethylation of the promoter. The benefit of targeting KIR3DL2 with lacutamab is being further explored in a randomized phase 2 study in peripheral T-cell lymphoma, including ATL (registered on https://clinicaltrials.gov as #NCT04984837). •KIR3DL2, with expression triggered by HTLV-1 infection, is a novel diagnostic marker of acute-type ATL.•The lacutamab monoclonal anti-KIR3DL2 antibody may be an effective strategy to treat ATL and is under study for relapsed/refractory PTCL. [Display omitted]
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.2022016765