1. Immunology/Inflammation
  2. Transmembrane Glycoprotein
  3. HB0030

HB0030 is a TIGIT inhibitor with antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) activities. HB0030 enhances the expression of activation markers in natural killer (NK) cells, promotes the killing of regulatory T cells (Tregs), and reduces the proportion of FoxP3+ Treg in tumor-infiltrating lymphocytes. The combination of HB0030 with the anti-PD-L1/VEGF bispecific antibody HB0025 further enhances tumor suppression efficacy. HB0030 can be used in studies related to colorectal cancer, pancreatic adenocarcinoma, hepatocellular carcinoma, bladder cancer, breast cancer, non-small cell lung cancer, and advanced solid tumors.

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HB0030

HB0030 Chemical Structure

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Description

HB0030 is a TIGIT inhibitor with antibody-dependent cellular cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) activities. HB0030 enhances the expression of activation markers in natural killer (NK) cells, promotes the killing of regulatory T cells (Tregs), and reduces the proportion of FoxP3+ Treg in tumor-infiltrating lymphocytes. The combination of HB0030 with the anti-PD-L1/VEGF bispecific antibody HB0025 further enhances tumor suppression efficacy. HB0030 can be used in studies related to colorectal cancer, pancreatic adenocarcinoma, hepatocellular carcinoma, bladder cancer, breast cancer, non-small cell lung cancer, and advanced solid tumors[1][2].

Isotype

Human IgG1 kappa

Recommend Isotype Controls
Species Reactivity

Human

In Vitro

HB0030 (10-5-103 nM; 5 hours) potently mediates NK cell-dependent lysis of human TIGIT-expressing Jurkat cells in vitro, with greater cytotoxic activity than HB0036[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Cytotoxicity Assay[1]

Cell Line: human TIGIT-expressing Jurkat cells, pre-activated human NK cells
Concentration: 10-5-103 nM
Incubation Time: 5 hours
Result: Mediated dose-dependent NK cell killing of TIGIT-expressing Jurkat cells.
Showed stronger cytotoxic activity compared to HB0036.
In Vivo

HB0030 (500 mg/kg; i.p.; single dose) significantly reduces intratumoral FoxP3+ Treg proportions in hPD-L1+ MC38 tumors in humanized C57BL/6 mice[1].
HB0030 (10 mg/kg; i.p.; twice weekly; 4 total doses) combined with anti-PD-L1 antibody 900458 significantly reduces tumor volume and weight, and increases intratumoral IFN-γ and TNF-α levels, in CT26-hPD-L1 tumor-bearing humanized BALB/c mice[1].
HB0030 (3 mg/kg; i.p.; twice weekly; 4 total doses) monotherapy significantly inhibits H22-hPD-L1 tumor growth with a 50% partial response rate, and its combination with HB0025 enhances efficacy to an 87.5% partial response rate in humanized BALB/c mice[1].
HB0030 (3 mg/kg; i.p.; twice weekly; 4 total doses) combined with HB0025 significantly enhances tumor inhibition compared to monotherapies in hPD-L1-expressing MC38 tumor-bearing humanized C57BL/6 mice[1].
HB0030 (10 mg/kg; i.p.; twice weekly; 4 total doses) combined with HB0025 significantly enhances tumor inhibition compared to monotherapies in hPD-L1-expressing EMT6 tumor-bearing humanized BALB/c mice[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: hTIGIT/hPD-L1/hPD-1 humanized C57BL/6 (subcutaneously inoculated with 1×106 wild-type hPD-L1- MC38 cells on left flank and 1×106 hPD-L1+ MC38 cells on right flank, grown to ~200 mm3 over 13 days)[1]
Dosage: 500 mg/kg
Administration: i.p.; single dose
Result: Significantly reduced the proportion of FoxP3+ regulatory T cells (Tregs) in tumor-infiltrating lymphocytes within hPD-L1+ MC38 tumors.
No significant Treg reduction was observed in hPD-L1- MC38 tumors.
Animal Model: hPD-1/hPD-L1/hTIGIT humanized BALB/c (subcutaneously inoculated with 1×106 CT26-hPD-L1 cells, grown to average volume of 160 mm3)[1]
Dosage: 10 mg/kg (in combination with 10 mg/kg anti-PD-L1 antibody 900458)
Administration: i.p.; twice weekly; 4 total doses
Result: Significantly reduced tumor volume and tumor weight compared to control.
Elevated intratumoral IFN-γ and TNF-α levels compared to control, though lower than levels in the HB0036 monotherapy group.
Animal Model: hPD-1/hPD-L1/hTIGIT humanized BALB/c (subcutaneously inoculated with 1×106 H22-hPD-L1 cells, grown to average volume of 100 mm3)[1]
Dosage: 3 mg/kg (monotherapy; in combination with 2 mg/kg anti-PD-L1/VEGF bispecific antibody HB0025)
Administration: i.p.; twice weekly; 4 total doses
Result: Showed significant tumor inhibition compared to isotype control, with a partial response rate of 3/6.
Combination with HB0025 showed superior tumor suppression compared to either monotherapy, with a partial response rate of 7/8.
Gene ID

201633  [NCBI]

Accession
Target

TIGIT

Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

The product can be reconstituted/diluted with sterile PBS or saline.

Formulation

Please refer to the lot-specific COA for specific buffer information.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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HB0030
Cat. No.:
HY-P992361
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