scholarly journals Mechanisms of the Antitumor Activity of Human Vγ9Vδ2 T Cells in Combination With Zoledronic Acid in a Preclinical Model of Neuroblastoma

2013 ◽  
Vol 21 (5) ◽  
pp. 1034-1043 ◽  
Author(s):  
Emma Di Carlo ◽  
Paola Bocca ◽  
Laura Emionite ◽  
Michele Cilli ◽  
Giuseppe Cipollone ◽  
...  
2013 ◽  
Vol 331 (2) ◽  
pp. 174-182 ◽  
Author(s):  
Hiroki Goto ◽  
Kouki Matsuda ◽  
Pattaravadee Srikoon ◽  
Ryusho Kariya ◽  
Shinichiro Hattori ◽  
...  

Tumor Biology ◽  
2015 ◽  
Vol 37 (6) ◽  
pp. 7333-7344 ◽  
Author(s):  
L. Sun ◽  
Y. Li ◽  
Z. Jiang ◽  
J. Zhang ◽  
H. Li ◽  
...  

2011 ◽  
Vol 187 (4) ◽  
pp. 1578-1590 ◽  
Author(s):  
Barbara Castella ◽  
Chiara Riganti ◽  
Francesca Fiore ◽  
Francesca Pantaleoni ◽  
Maria Elisa Canepari ◽  
...  

AIDS ◽  
2009 ◽  
Vol 23 (5) ◽  
pp. 555-565 ◽  
Author(s):  
Fabrizio Poccia ◽  
Cristiana Gioia ◽  
Federico Martini ◽  
Alessandra Sacchi ◽  
Paola Piacentini ◽  
...  

2017 ◽  
Vol 386 ◽  
pp. 141-150 ◽  
Author(s):  
Aneta Zysk ◽  
Mark O. DeNichilo ◽  
Vasilios Panagopoulos ◽  
Irene Zinonos ◽  
Vasilios Liapis ◽  
...  

Blood ◽  
2021 ◽  
Vol 138 (Supplement 1) ◽  
pp. 2266-2266
Author(s):  
Roeland Lameris ◽  
Jurjen M Ruben ◽  
Iris de Weerdt ◽  
Rob Roovers ◽  
Niels W.C.J. van de Donk ◽  
...  

Abstract Background. Bispecific antibodies that target tumors by engaging innate-like T cell subsets with inherent antitumor activity, such as Vγ9Vδ2-T and type 1 natural killer T (NKT) cells, may combine high therapeutic efficacy with limited off-tumor toxicity. Type 1 NKT cells respond to self and foreign (glyco)lipid antigens presented in the context of the MHC class I like molecule CD1d which is expressed on various malignancies. Vγ9Vδ2-T cells respond to intracellular accumulation of phosphoantigens in cancer cells by sensing conformational alterations in the butyrophilin (BTN) 2A1-3A1 complex. CD1d is expressed by the majority of patients with CLL and MM, while expression in AML is most pronounced on (myelo)monocytic subtypes. Methods. LAVA-051 is a 27kD humanized bispecific single domain antibody (bsVHH) that directly engages CD1d and the Vδ2-TCR chain of Vγ9Vδ2-T cells. The anti-CD1d VHH specifically stabilizes the interaction between CD1d and the type 1 NKT cell TCR and thereby triggers strong activation of type 1 NKT cells (Nature Cancer 2020;1:1054-1065). Vγ9Vδ2-T and type 1 NKT effector cell activation, proliferation, cytokine production and target cell lysis were assessed in in vitro, ex vivo, and in vivo studies. Due to lack of cross reactivity of LAVA-051 with non-human primate (NHP) CD1d and Vγ9Vδ2-T cells, a cross-reactive surrogate bispecific engager was generated to assess tolerability, pharmacokinetic (PK) and pharmacodynamic (PD) parameters. Results. The CD1d-Vδ2 bsVHH LAVA-051 triggers activation of both Vγ9Vδ2-T and type 1 NKT cells (EC 50 4 pM for Vγ9Vδ2-T and 366 pM for type 1 NKT; induction of > 80% degranulation in 4h assays) and mediates potent killing of CD1d expressing tumor cells by engagement of Vγ9Vδ2-T and/or type 1 NKT cells (EC 50 1 pM for Vγ9Vδ2-T and 216 pM for type 1 NKT; > 85% target cell lysis in 16h assays at a low 1:2 E:T ratio). Further, LAVA-051 triggered pro-inflammatory cytokine production, proliferation of Vγ9Vδ2-T and type 1 NKT cells, and exerted substantial antitumor activity against patient AML, CLL and MM cells that express CD1d and improved survival in in vivo T-ALL, AML and MM mouse models. Multiple dose studies in NHP (7 daily doses up to 1 mg/kg iv) showed clear Vγ9Vδ2-T cell engagement and some cytokine release after the first administration, but no clinical, laboratory, or histopathological toxicity. Reflecting the low molecular size of this bispecific engager, PK studies revealed a short plasma half-life which was however compensated for by prolonged (up to 5 days) binding of the engager to peripheral blood Vγ9Vδ2-T cells allowing intermittent dosing. Conclusions. In this study, we demonstrate that the CD1d-Vδ2 bsVHH LAVA-051 triggers activation of both type 1 NKT and Vγ9Vδ2-T cells, which translates directly into antitumor activity. Based on the expression of CD1d in CLL, MM, and AML, the strong preclinical activity of LAVA-051 against CD1d-expresssing tumors, and the favorable tolerability profile of the surrogate engager in NHP, LAVA-051 is currently evaluated in a first-in-human clinical Phase 1/2a study in patients with CD1d-expressing CLL, MM, or AML refractory to prior therapy (NCT04887259). Disclosures Lameris: Lava Therapeutics: Honoraria, Patents & Royalties, Research Funding. Ruben: Lava Therapeutics: Current Employment, Honoraria, Research Funding. Weerdt: LAVA Therapeutics: Research Funding. Roovers: LAVA Therapeutics: Current Employment, Current equity holder in publicly-traded company. van de Donk: Janssen Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees, Research Funding; Celgene: Membership on an entity's Board of Directors or advisory committees, Research Funding; Adaptive Biotechnologies: Membership on an entity's Board of Directors or advisory committees; Amgen: Membership on an entity's Board of Directors or advisory committees, Research Funding; Takeda: Membership on an entity's Board of Directors or advisory committees; Bristol Myers Squibb: Membership on an entity's Board of Directors or advisory committees, Research Funding; Novartis: Membership on an entity's Board of Directors or advisory committees; Roche: Membership on an entity's Board of Directors or advisory committees; Bayer: Membership on an entity's Board of Directors or advisory committees; Servier: Membership on an entity's Board of Directors or advisory committees; Cellectis: Research Funding. Broyl: Amgen: Honoraria; Bristol-Meyer Squibb: Honoraria; Celgene: Honoraria; Janssen Pharmaceuticals: Honoraria; Sanofi: Honoraria. Kater: Abbvie: Honoraria, Other: Ad Board, Research Funding; Janssen, AstraZeneca: Other: Ad Board, steering committee, Research Funding; Genmab, LAVA: Other: Ad Board, Steering Committee; BMS, Roche/Genentech: Other: Ad Board, , Research Funding. Riedl: LAVA THerapeutics: Current Employment, Current equity holder in publicly-traded company; Genmab BV: Current equity holder in publicly-traded company. Iglesias: LAVA therapeutics: Current Employment. Winograd: LAVA therapeutics: Current Employment, Current equity holder in publicly-traded company, Membership on an entity's Board of Directors or advisory committees; Celgene: Ended employment in the past 24 months; BMS: Current equity holder in publicly-traded company. Adang: LAVA therapeutics: Current Employment, Current equity holder in publicly-traded company, Honoraria, Membership on an entity's Board of Directors or advisory committees. de Gruijl: LAVA therapeutics: Current equity holder in publicly-traded company, Membership on an entity's Board of Directors or advisory committees, Patents & Royalties; DCPrime: Membership on an entity's Board of Directors or advisory committees; Macrophage Pharma: Membership on an entity's Board of Directors or advisory committees, Research Funding; Partner Tx: Membership on an entity's Board of Directors or advisory committees; Idera Pharmaceuticals: Research Funding; ORCA Therapeutics: Patents & Royalties. Parren: Lava Therapeutics: Current Employment, Current equity holder in publicly-traded company, Membership on an entity's Board of Directors or advisory committees, Patents & Royalties; Sparring Bioconsult BV: Membership on an entity's Board of Directors or advisory committees; Genmab: Patents & Royalties; Roche: Consultancy. Vliet: Lava Therapeutics: Current Employment, Current equity holder in publicly-traded company, Honoraria, Membership on an entity's Board of Directors or advisory committees, Patents & Royalties, Research Funding; Glycostem: Research Funding.


2020 ◽  
Vol 8 (Suppl 3) ◽  
pp. A303-A303
Author(s):  
George Blumenschein ◽  
Siddhartha Devarakonda ◽  
Melissa Johnson ◽  
Victor Moreno ◽  
Justin Gainor ◽  
...  

BackgroundADP-A2M10 SPEAR T-cells are genetically engineered autologous T-cells that express a high affinity MAGE-A10-specific T-cell receptor targeting MAGE-A10+tumors in the context of HLA-A*02. This trial is now complete (NCT02592577).MethodsThis first-in-human dose escalation trial utilized a modified 3+3 design to evaluate safety and antitumor activity. Eligible patients (pts) were HLA-A*02+ with advanced non-small cell lung cancer (NSCLC) expressing MAGE-A10. Pts underwent apheresis; T-cells were isolated, transduced with a lentiviral vector containing the TCR targeting MAGE-A10, and expanded. Pts underwent lymphodepletion (LD) with varying doses/schedules of fludarabine (Flu) and cyclophosphamide (Cy) prior to receiving ADP-A2M10. ADP-A2M10 was administered at Dose Level (DL) 1= 0.1×109, DL2 0.5–1.2×109, and DL3/Expansion= 1.2–15×109 transduced cells.ResultsAs of Jan 10, 2020, 11 pts (6 male/5 female) with NSCLC (3 squamous cell, 7 adenocarcinoma, 1 adenosquamous) were treated. Five, 3 and 3 pts received cells at DL1, DL2, and DL3/Expansion, respectively. The most frequently reported adverse events ≥ Grade 3 were lymphopenia (11), leukopenia (9), neutropenia (8), anemia (6), thrombocytopenia (5), and hyponatremia (5). Three pts reported CRS (Grades 1, 2, and 4, respectively). One pt received the highest dose of LD (Flu 30 mg/m2 Day 1 4 and Cy 1800 mg/m2 Day 1–2) prior to a second infusion and had a partial response (PR). This pt subsequently developed aplastic anemia and died. Responses included: 1 pt – PR, 3 pts - stable disease, 2 pts – progressive disease, 1 pt - too early to determine, 4 pts - off-study prior to tumor assessment. SPEAR T-cells were detectable in peripheral blood from pts at each dose level, and in tumor tissue from pts at DL1 and DL3.ConclusionsADP-A2M10 SPEAR T-cells have shown acceptable safety and no evidence of toxicity related to off-target binding or alloreactivity. Given the minimal antitumor activity and the discovery that MAGE-A10 expression frequently overlaps with MAGE-A4 expression, the clinical program has closed. Several trials with SPEAR T-cells targeting MAGE-A4 are ongoing (https://bit.ly/35htsZK).Trial RegistrationNCT02592577Ethics ApprovalThe trial was conducted in accordance with the principles of the Declaration of Helsinki and the International Conference on Harmonization Good Clinical Practice guidelines and was approved by local authorities. An independent ethics committee or institutional review board approved the clinical protocol at each participating center. All the patients provided written informed consent before study entry.


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