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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with <t>mKRAS-VAX,</t> a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.
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a Treatment schema for patients treated with mKRAS-VAX, a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.

Journal: Nature Communications

Article Title: Mutant KRAS vaccine with dual checkpoint blockade in resected pancreatic cancer: a phase I trial

doi: 10.1038/s41467-026-68324-4

Figure Lengend Snippet: a Treatment schema for patients treated with mKRAS-VAX, a pool of 6 synthetic long mKRAS peptides in the adjuvant setting. Patients receive four doses of 0.3 mg peptide/dose with 5ug polyICLC during the priming phase followed by booster vaccines every 8 weeks. Ipilimumab (1 mg/kg) and Nivolumab (3 mg/kg) were given for the first four doses followed by Nivolumab (480 mg) maintenance doses every four weeks. Created in BioRender. Huff, A. ( https://BioRender.com/1vglal1 ) ( b ) Clinical event timeline for each patient enrolled and vaccinated. c IFNγ ELISPOT assay of PMBCs collected at baseline and post-vaccination time points after restimulation with vehicle only control (unstimulated) or 2ug/mL control peptide or individual mKRAS long peptides overnight. Statistics of IFNγ spot forming units detected after each mKRAS peptide stimulation relative to control peptide are shown in Supplementary Table . Data are shown as mean ( n = 3) and upper limit of SD.

Article Snippet: In a first-in-human phase I clinical trial (ClinicalTrials.gov: NCT04117087 ), we tested mKRAS-VAX in combination with nivolumab (anti–PD-1 antibody) and ipilimumab (anti–CTLA–4 antibody) in patients with resected PDAC.

Techniques: Adjuvant, Vaccines, Enzyme-linked Immunospot, Control