pe anti mouse il 17a Search Results


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Miltenyi Biotec anti il 17a pe antibody
(A) Arthritis scores of mice were measured every 3 days starting at 21 days after the first immunization. (B) DBA1/J mice showed deformation and swelling of the toe and ankle joints. (C) Paraffin-embedded sections of CIA mice joint were stained with hematoxylin and eosin. (D) Histological analysis was performed based on the analysis criteria: inflammation, synovial hyperplasia, pannus formation, and erosion of cartilage and bone. (E) The protein levels of IL-6, IL-1β <t>and</t> <t>IL-17</t> in CIA mouse serum were measured using ELISA. Data are presented as mean ± SEM. # p <0.05 vs. normal group, * p <0.05, ** p <0.01, and *** p <0.005 vs. CIA control group.
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Multi Sciences (Lianke) Biotech Co Ltd anti mouse il 17a 17b7 ab
(A) Arthritis scores of mice were measured every 3 days starting at 21 days after the first immunization. (B) DBA1/J mice showed deformation and swelling of the toe and ankle joints. (C) Paraffin-embedded sections of CIA mice joint were stained with hematoxylin and eosin. (D) Histological analysis was performed based on the analysis criteria: inflammation, synovial hyperplasia, pannus formation, and erosion of cartilage and bone. (E) The protein levels of IL-6, IL-1β <t>and</t> <t>IL-17</t> in CIA mouse serum were measured using ELISA. Data are presented as mean ± SEM. # p <0.05 vs. normal group, * p <0.05, ** p <0.01, and *** p <0.005 vs. CIA control group.
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To model EA or MGA respectively, Balb/c or Il4ra -/- mice were given five intranasal (i.n.) challenges with 100ug house dust mite (HDM) extract every week (followed by two days resting) for three consecutive weeks. A final i.n. HDM challenge was given 24 hours prior to harvest. ( A ) Lung sections were stained and representative Masson trichrome (collagen), α-smooth muscle actin (αSMA), and hematoxylin and eosin (H&E) sections and accompanying quantifications are shown. ( B ) Airway resistance to increasing doses of methacholine exposure (6-8 mice per group). (C) Expression of mRNA for IL13 and IL17, assessed by quantitative PCR analyses of lung samples. mRNA expression was calculated relative to GAPDH for 5 mice per group. ( D ) Number of neutrophils or eosinophils in the left lung lobe of EA or MGA induced mice, as assessed by flow cytometry. ( E ) MGA-induced animals were treated with 50ug dexamethasone intratracheally one hour prior to each allergen challenge, beginning on day 7. Lung sections were stained and representative Masson trichrome and αSMA sections and accompanying quantifications are shown. ( F ) Number of neutrophils or eosinophils in the left lung lobe of MGA induced mice treated with or without dexamethasone, as assessed by flow cytometry. ( G ) MGA-induced animals were treated with <t>100ug</t> <t>anti-IL17A</t> or matching isotype control i.p. beginning on day 7 and continuing every other day until harvest. Lung sections were stained, and representative H&E sections and accompanying quantifications are shown. Trichrome data show area of interest values covering full lung section of 6 individual mice per condition. αSMA data show mean values of all bronchi scored from 6 mice per condition. Data are representative of 3 independent experiments. *P < 0.05, **P < 0.005, ***P < 0.0005, ****P < 0.00005; HPF, high-power field; ns, nonsignificant.
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Expression of CX3CL1 and Th17 Cells in PD mice. (A) Co-localization of CX3CL1 and <t>IL-17A</t> in immunofluorescence images, along with quantitative analysis and serum CX3CL1 levels ( n = 4). (B) Western blot and quantitative analysis of CX3CL1 and IL-17A ( n = 5). # P < 0.05 vs. Model group; * P < 0.05 vs. Control group. CRSJ-L, low-dose Congrong Shujing Granules; CRSJ-M, medium-dose Congrong Shujing Granules; CRSJ-H, high-dose Congrong Shujing Granules.
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Bio X Cell monoclonal antibody targeting il 17a
( A ) Immunofluorescence staining and quantification of <t>IL-17a</t> + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.
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Elabscience Biotechnology pe anti mouse il
( A ) Immunofluorescence staining and quantification of <t>IL-17a</t> + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.
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( A ) Immunofluorescence staining and quantification of <t>IL-17a</t> + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.
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Elabscience Biotechnology anti mouse il 17a elab fluor 647
( A ) Immunofluorescence staining and quantification of <t>IL-17a</t> + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.
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Rockland Immunochemicals non competing biotinylated mouse anti human il 17a antibody
Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.
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Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.
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Miltenyi Biotec anti il 17 apc fluorochrome tagged mouse monoclonal antibodies mab
Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.
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Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.
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Image Search Results


(A) Arthritis scores of mice were measured every 3 days starting at 21 days after the first immunization. (B) DBA1/J mice showed deformation and swelling of the toe and ankle joints. (C) Paraffin-embedded sections of CIA mice joint were stained with hematoxylin and eosin. (D) Histological analysis was performed based on the analysis criteria: inflammation, synovial hyperplasia, pannus formation, and erosion of cartilage and bone. (E) The protein levels of IL-6, IL-1β and IL-17 in CIA mouse serum were measured using ELISA. Data are presented as mean ± SEM. # p <0.05 vs. normal group, * p <0.05, ** p <0.01, and *** p <0.005 vs. CIA control group.

Journal: PLOS ONE

Article Title: Anti-inflammatory effect of the combined treatment of LMT-28 and kaempferol in a collagen-induced arthritis mouse model

doi: 10.1371/journal.pone.0302119

Figure Lengend Snippet: (A) Arthritis scores of mice were measured every 3 days starting at 21 days after the first immunization. (B) DBA1/J mice showed deformation and swelling of the toe and ankle joints. (C) Paraffin-embedded sections of CIA mice joint were stained with hematoxylin and eosin. (D) Histological analysis was performed based on the analysis criteria: inflammation, synovial hyperplasia, pannus formation, and erosion of cartilage and bone. (E) The protein levels of IL-6, IL-1β and IL-17 in CIA mouse serum were measured using ELISA. Data are presented as mean ± SEM. # p <0.05 vs. normal group, * p <0.05, ** p <0.01, and *** p <0.005 vs. CIA control group.

Article Snippet: The cells were incubated with anti-IL-17A-PE antibody (Miltenyi Biotec) or anti-mouse FOXP3 antibody (Invitrogen, Waltham, MA, USA) diluted in 1× permeabilization buffer (eBioscience) for 30 min at 4°C in the dark.

Techniques: Staining, Enzyme-linked Immunosorbent Assay, Control

To model EA or MGA respectively, Balb/c or Il4ra -/- mice were given five intranasal (i.n.) challenges with 100ug house dust mite (HDM) extract every week (followed by two days resting) for three consecutive weeks. A final i.n. HDM challenge was given 24 hours prior to harvest. ( A ) Lung sections were stained and representative Masson trichrome (collagen), α-smooth muscle actin (αSMA), and hematoxylin and eosin (H&E) sections and accompanying quantifications are shown. ( B ) Airway resistance to increasing doses of methacholine exposure (6-8 mice per group). (C) Expression of mRNA for IL13 and IL17, assessed by quantitative PCR analyses of lung samples. mRNA expression was calculated relative to GAPDH for 5 mice per group. ( D ) Number of neutrophils or eosinophils in the left lung lobe of EA or MGA induced mice, as assessed by flow cytometry. ( E ) MGA-induced animals were treated with 50ug dexamethasone intratracheally one hour prior to each allergen challenge, beginning on day 7. Lung sections were stained and representative Masson trichrome and αSMA sections and accompanying quantifications are shown. ( F ) Number of neutrophils or eosinophils in the left lung lobe of MGA induced mice treated with or without dexamethasone, as assessed by flow cytometry. ( G ) MGA-induced animals were treated with 100ug anti-IL17A or matching isotype control i.p. beginning on day 7 and continuing every other day until harvest. Lung sections were stained, and representative H&E sections and accompanying quantifications are shown. Trichrome data show area of interest values covering full lung section of 6 individual mice per condition. αSMA data show mean values of all bronchi scored from 6 mice per condition. Data are representative of 3 independent experiments. *P < 0.05, **P < 0.005, ***P < 0.0005, ****P < 0.00005; HPF, high-power field; ns, nonsignificant.

Journal: bioRxiv

Article Title: The metabolic reprogramming of T cells controls airway remodeling in severe asthma

doi: 10.64898/2026.03.19.712985

Figure Lengend Snippet: To model EA or MGA respectively, Balb/c or Il4ra -/- mice were given five intranasal (i.n.) challenges with 100ug house dust mite (HDM) extract every week (followed by two days resting) for three consecutive weeks. A final i.n. HDM challenge was given 24 hours prior to harvest. ( A ) Lung sections were stained and representative Masson trichrome (collagen), α-smooth muscle actin (αSMA), and hematoxylin and eosin (H&E) sections and accompanying quantifications are shown. ( B ) Airway resistance to increasing doses of methacholine exposure (6-8 mice per group). (C) Expression of mRNA for IL13 and IL17, assessed by quantitative PCR analyses of lung samples. mRNA expression was calculated relative to GAPDH for 5 mice per group. ( D ) Number of neutrophils or eosinophils in the left lung lobe of EA or MGA induced mice, as assessed by flow cytometry. ( E ) MGA-induced animals were treated with 50ug dexamethasone intratracheally one hour prior to each allergen challenge, beginning on day 7. Lung sections were stained and representative Masson trichrome and αSMA sections and accompanying quantifications are shown. ( F ) Number of neutrophils or eosinophils in the left lung lobe of MGA induced mice treated with or without dexamethasone, as assessed by flow cytometry. ( G ) MGA-induced animals were treated with 100ug anti-IL17A or matching isotype control i.p. beginning on day 7 and continuing every other day until harvest. Lung sections were stained, and representative H&E sections and accompanying quantifications are shown. Trichrome data show area of interest values covering full lung section of 6 individual mice per condition. αSMA data show mean values of all bronchi scored from 6 mice per condition. Data are representative of 3 independent experiments. *P < 0.05, **P < 0.005, ***P < 0.0005, ****P < 0.00005; HPF, high-power field; ns, nonsignificant.

Article Snippet: To block IL-17 signaling, 100ug anti-IL17A (17F3; BioXCell) or matching isotype control (MOPC-21; BioXCell) were given intraperitoneally (i.p.) to HDM induced Ilr4a -/- mice beginning on day 7 and continuing every other day for a total of 7 injections.

Techniques: Staining, Expressing, Real-time Polymerase Chain Reaction, Flow Cytometry, Control

Expression of CX3CL1 and Th17 Cells in PD mice. (A) Co-localization of CX3CL1 and IL-17A in immunofluorescence images, along with quantitative analysis and serum CX3CL1 levels ( n = 4). (B) Western blot and quantitative analysis of CX3CL1 and IL-17A ( n = 5). # P < 0.05 vs. Model group; * P < 0.05 vs. Control group. CRSJ-L, low-dose Congrong Shujing Granules; CRSJ-M, medium-dose Congrong Shujing Granules; CRSJ-H, high-dose Congrong Shujing Granules.

Journal: Frontiers in Aging Neuroscience

Article Title: Systems-level molecular and immunological evidence identifies Th17/Treg modulation as a key mechanism of CRSJ’s neuroprotection in Parkinson’s disease

doi: 10.3389/fnagi.2026.1764634

Figure Lengend Snippet: Expression of CX3CL1 and Th17 Cells in PD mice. (A) Co-localization of CX3CL1 and IL-17A in immunofluorescence images, along with quantitative analysis and serum CX3CL1 levels ( n = 4). (B) Western blot and quantitative analysis of CX3CL1 and IL-17A ( n = 5). # P < 0.05 vs. Model group; * P < 0.05 vs. Control group. CRSJ-L, low-dose Congrong Shujing Granules; CRSJ-M, medium-dose Congrong Shujing Granules; CRSJ-H, high-dose Congrong Shujing Granules.

Article Snippet: For Th17 staining, cells were labeled with FITC-anti-CD4 and APC-anti-IL-17A antibodies (Elabscience, No. E-AB-F1199E).

Techniques: Expressing, Immunofluorescence, Western Blot, Control

( A ) Immunofluorescence staining and quantification of IL-17a + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.

Journal: The Journal of Clinical Investigation

Article Title: Pharmacological targeting of the IL-17/neutrophil axis attenuates calcific deposits in rat models of calciphylaxis

doi: 10.1172/JCI190369

Figure Lengend Snippet: ( A ) Immunofluorescence staining and quantification of IL-17a + cells in skin tissue from rats treated with DHT p.o. + FeCl 3 s.c. or vehicle p.o. + H 2 O s.c. (representative images; n = 5 animals per group). Scale bar: 50 μm. ( B ) Schematic of the IL-17a mAb experimental timeline. ( C ) Gross images of dorsal skin lesions. Black arrowheads show visible regions of calcification. ( D ) Representative von Kossa–stained images of rat dermal tissue highlighting calcified regions (arrowheads). Quantification of calcified percentage in the IL-17a mAb–treated group ( n = 12) compared with IgG control ( n = 8). ( E ) Top 5 KEGG pathways enriched in DEGs between IgG-treated ( n = 3 animals) and IL-17a mAb–treated rats following DHT p.o. + FeCl 3 s.c. ( n = 3 animals). ( F ) Enriched genes in IL-17 signaling pathway. Data are represented as mean ± SEM. *** P < 0.001, 2-tailed Student’s t test.

Article Snippet: To determine the specific role of IL-17 in mediating calcific deposits, we injected the animals with a monoclonal antibody targeting IL-17a (IL-17a mAb, Bio X Cell, BP0173).

Techniques: Immunofluorescence, Staining, Control

Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Summary of JNJ-8104, golimumab and CNTO 6785 in vitro target-binding kinetics and activities.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques: In Vitro

Inhibition of in vitro inflammatory responses mediated by endogenous TNF and IL-17A. Human rheumatoid arthritis fibroblast-like synovial cells (RA-FLS) were cocultured with in vitro differentiated T h 17/T h 1 cells. Various concentrations of JNJ-8104, CNTO 9809 (parental anti-TNF), CNTO 4782 (parental anti-IL-17A) or equal-molar fixed-ratio combination of CNTO 9809 and CNTO 4782 were incubated with the coculture for 48 hours. Endogenous TNF and IL-17A-mediated production of IL-6 (a) and GROα (b) in the supernatants were measured.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Inhibition of in vitro inflammatory responses mediated by endogenous TNF and IL-17A. Human rheumatoid arthritis fibroblast-like synovial cells (RA-FLS) were cocultured with in vitro differentiated T h 17/T h 1 cells. Various concentrations of JNJ-8104, CNTO 9809 (parental anti-TNF), CNTO 4782 (parental anti-IL-17A) or equal-molar fixed-ratio combination of CNTO 9809 and CNTO 4782 were incubated with the coculture for 48 hours. Endogenous TNF and IL-17A-mediated production of IL-6 (a) and GROα (b) in the supernatants were measured.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques: Inhibition, In Vitro, Incubation

Inhibition of rhTNF- and rhIL-17A-induced Cellular Influx by JNJ-8104 in the Airway Lumen of Mice. Mice were intranasally instilled with rhTNF- and rhIL-17A in combination. After 6 h their lungs were lavaged and total numbers of BAL cells (a) and neutrophils (b) were enumerated as detailed in “Materials & Methods.” Mice were injected intraperitoneally with the test mAbs or isotype control18 hours prior to cytokines challenge. Data are represented as mean ± SEM; N = 6–7 mice/group.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Inhibition of rhTNF- and rhIL-17A-induced Cellular Influx by JNJ-8104 in the Airway Lumen of Mice. Mice were intranasally instilled with rhTNF- and rhIL-17A in combination. After 6 h their lungs were lavaged and total numbers of BAL cells (a) and neutrophils (b) were enumerated as detailed in “Materials & Methods.” Mice were injected intraperitoneally with the test mAbs or isotype control18 hours prior to cytokines challenge. Data are represented as mean ± SEM; N = 6–7 mice/group.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques: Inhibition, Injection

Observed serum concentrations versus time profiles of Total mAb (a), total TNF (b), and Total IL-17A (c) following IV administration of golimumab (parental anti-TNF), CNTO 6785 (anti-IL-17A with identical parental Fab arms) or JNJ-8104 at the specified dose levels in cynomolgus monkeys. Data are represented as mean ± SD.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Observed serum concentrations versus time profiles of Total mAb (a), total TNF (b), and Total IL-17A (c) following IV administration of golimumab (parental anti-TNF), CNTO 6785 (anti-IL-17A with identical parental Fab arms) or JNJ-8104 at the specified dose levels in cynomolgus monkeys. Data are represented as mean ± SD.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques:

Estimated JNJ-8104, CNTO148 and CNTO 6785 cynomolgus monkey PK/TE model parameters (mean, residual standard error%) and predicted human parameters.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Estimated JNJ-8104, CNTO148 and CNTO 6785 cynomolgus monkey PK/TE model parameters (mean, residual standard error%) and predicted human parameters.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques:

PK/TE model fitting of PK, total IL-17A and Free IL-17A profiles following IV administration of JNJ-8104 (a) and CNTO 6785 (b) in cynomolgus monkeys. Symbols = Observed individual data; Lines = Mean model prediction.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: PK/TE model fitting of PK, total IL-17A and Free IL-17A profiles following IV administration of JNJ-8104 (a) and CNTO 6785 (b) in cynomolgus monkeys. Symbols = Observed individual data; Lines = Mean model prediction.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques:

Comparison of observed and model-predicted Total IL-17A profiles following a single IV administration of JNJ-8104 at 0.1, 0.3, 1, 3 and 10 mg/kg (a−e) normal human subjects. Symbols = Observed individual data; Solid lines = Mean model prediction based on cyno PK/TE model parameters and allometric scaling for human PK; Dotted lines = Mean model prediction based on estimated JNJ-8104 human PK parameters from FIH data with cyno-based in vivo KD.

Journal: mAbs

Article Title: Characterization of concurrent target suppression by JNJ-61178104, a bispecific antibody against human tumor necrosis factor and interleukin-17A

doi: 10.1080/19420862.2020.1770018

Figure Lengend Snippet: Comparison of observed and model-predicted Total IL-17A profiles following a single IV administration of JNJ-8104 at 0.1, 0.3, 1, 3 and 10 mg/kg (a−e) normal human subjects. Symbols = Observed individual data; Solid lines = Mean model prediction based on cyno PK/TE model parameters and allometric scaling for human PK; Dotted lines = Mean model prediction based on estimated JNJ-8104 human PK parameters from FIH data with cyno-based in vivo KD.

Article Snippet: The concentrations of total IL-17A in cyno and human serum were measured with similar MSD assays, except using a non-competing biotinylated mouse anti-human IL-17A antibody (Clone 4H1524.1, Rockland) for capture and a non-competing ruthenium-labeled mouse IgG1 anti-human IL-17A antibody (Clone 41802, R&D Systems) for detection.

Techniques: Comparison, In Vivo