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murine colon carcinoma cell lines  (ATCC)


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    ATCC murine colon carcinoma cell lines
    Murine Colon Carcinoma Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 3500 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/murine colon carcinoma cell lines/product/ATCC
    Average 99 stars, based on 3500 article reviews
    murine colon carcinoma cell lines - by Bioz Stars, 2026-03
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    99
    ATCC murine colon carcinoma cell lines
    Murine Colon Carcinoma Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/murine colon carcinoma cell lines/product/ATCC
    Average 99 stars, based on 1 article reviews
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    99
    ATCC colon carcinoma cell line ct26
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Colon Carcinoma Cell Line Ct26, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC mouse colon carcinoma cell line ct26
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Mouse Colon Carcinoma Cell Line Ct26, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC colon carcinoma cell line ct26 cl25
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Colon Carcinoma Cell Line Ct26 Cl25, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC colon carcinoma cell line
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Colon Carcinoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC ct26 colon carcinoma cell line
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Ct26 Colon Carcinoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC ct26 mouse colon carcinoma cell line
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Ct26 Mouse Colon Carcinoma Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC 332 cell lines 333 murine colon carcinoma ct26 wt
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    332 Cell Lines 333 Murine Colon Carcinoma Ct26 Wt, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC murine colon carcinoma cell line ct26
    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse <t>CT26</t> tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.
    Murine Colon Carcinoma Cell Line Ct26, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/murine colon carcinoma cell line ct26/product/ATCC
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    DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse CT26 tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.

    Journal: Cell Reports Medicine

    Article Title: DF6215, an α-optimized IL-2-Fc fusion, expands immune effectors and drives robust preclinical anti-tumor activity

    doi: 10.1016/j.xcrm.2025.102518

    Figure Lengend Snippet: DF6215 mediates robust lymphocyte expansion and modulates the tumor microenvironment, resulting in potent anti-tumor activity (A) Kinetics of Ki-67 + immune subset counts in the blood after human (h)IgG1 isotype control or DF6215 administration (0.23 mg/kg in light blue and 1.35 mg/kg in dark blue) in naive BALB/c mice ( n = 3/group). Data represent the mean ± SEM. (B) Efficacy of DF6215 in the mouse CT26 tumor model. Individual tumor volumes, per caliper measurements, are shown with treatment days and frequencies as indicated (vertical dotted lines, QW schedule). The number of complete responders (CRs) in each DF6215 treatment group is noted within each image. n = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (log rank Mantel-Cox test: ∗∗∗ p < 0.001 and ∗∗∗∗ p < 0.0001). Top: mice were enrolled into treatment groups on day 11, when tumors averaged 218 mm 3 in size, and once weekly treatment began. Bottom: mice were enrolled into treatment groups on day 12, when tumors averaged 181 mm 3 in size, and once weekly treatment began. See also . (C and D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of DF6215 (0.675 mg/kg) or hIgG1 isotype after mice were enrolled into treatment groups when tumors averaged ∼218 mm 3 in size. (C) (Left) Absolute cell count quantification of indicated immune subsets in the tumor microenvironment 7 days post-treatment. Data shown are the mean ± SEM. (Right) Immune subset counts in tumors 96 h post-treatment. Significance for DF6215 relative to isotype by unpaired t test was noted as ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant. (D) Cytokines in blood as assessed by a Luminex proinflammatory panel 24 h post-treatment. Significance for DF6215 relative to isotype by one-way ANOVA with Tukey’s test is noted as ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, and ns, not significant.

    Article Snippet: The mouse melanoma cell line B16F10 and colon carcinoma cell line CT26 were obtained from ATCC.

    Techniques: Activity Assay, Control, Cell Characterization, Luminex

    DF6215 treatment augments anti-tumor activity compared to a non-⍺ IL-2-Fc (A) Efficacy of DF6215 monotherapy vs. non-⍺ IL-2 Fc monotherapy administered i.p. in the mouse CT26 tumor model. Individual tumor volumes are shown with treatment days and frequencies as indicated (vertical dotted lines). The number of complete responders (CRs) in each treatment group is noted in each image. N = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05; log rank Mantel-Cox test). Some of the DF6215 monotherapy data presented in to illustrate the dose response are included here to allow direct comparison with the non-α-binding IL-2-Fc, which was included as a comparator in the same experiment. See also . (B–D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of hIgG1 isotype, DF6215 (0.675 mg/kg), or non-⍺ IL-2-Fc (0.675 mg/kg). (B) The effector cell ratios of cells in the tumor microenvironment 96 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (C) Frequencies of CD69 + NK and CD8 + T cells in the tumor microenvironment 48 h post-treatment. (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (D) Frequencies of granzyme B + NK cells and CD8 + T cells in the tumor microenvironment 48 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test).

    Journal: Cell Reports Medicine

    Article Title: DF6215, an α-optimized IL-2-Fc fusion, expands immune effectors and drives robust preclinical anti-tumor activity

    doi: 10.1016/j.xcrm.2025.102518

    Figure Lengend Snippet: DF6215 treatment augments anti-tumor activity compared to a non-⍺ IL-2-Fc (A) Efficacy of DF6215 monotherapy vs. non-⍺ IL-2 Fc monotherapy administered i.p. in the mouse CT26 tumor model. Individual tumor volumes are shown with treatment days and frequencies as indicated (vertical dotted lines). The number of complete responders (CRs) in each treatment group is noted in each image. N = 10/group. Kaplan-Meier survival curves are shown, with the median survival indicated in brackets (∗∗∗ p < 0.001, ∗∗ p < 0.01, and ∗ p < 0.05; log rank Mantel-Cox test). Some of the DF6215 monotherapy data presented in to illustrate the dose response are included here to allow direct comparison with the non-α-binding IL-2-Fc, which was included as a comparator in the same experiment. See also . (B–D) BALB/c mice ( n = 10/group) were engrafted with CT26 and treated i.p. with a single dose of hIgG1 isotype, DF6215 (0.675 mg/kg), or non-⍺ IL-2-Fc (0.675 mg/kg). (B) The effector cell ratios of cells in the tumor microenvironment 96 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (C) Frequencies of CD69 + NK and CD8 + T cells in the tumor microenvironment 48 h post-treatment. (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test). (D) Frequencies of granzyme B + NK cells and CD8 + T cells in the tumor microenvironment 48 h post-treatment (∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001; one-way ANOVA with Tukey’s test).

    Article Snippet: The mouse melanoma cell line B16F10 and colon carcinoma cell line CT26 were obtained from ATCC.

    Techniques: Activity Assay, Comparison, Binding Assay