1. Immunology/Inflammation
  2. VISTA
  3. HMBD-002

HMBD-002 is an Fc-independent, non-depleting IgG4 subclass antibody that targets VISTA and VSIG3. It is widely used in research related to various solid tumors, including colon cancer, triple-negative breast cancer, and non-small cell lung cancer. HMBD-002 blocks the interactions of VISTA with VSIG3 and LRIG1, relieves immunosuppression without depleting VISTA-positive cells, activates the cytotoxic program of CD8+ T cells, and drives the type I interferon signaling pathway. HMBD-002 reprograms tumor-associated macrophages to the M1 phenotype, reduces tumor infiltration of inhibitory myeloid cells, thereby significantly inhibiting tumor growth and improving survival. HMBD-002 is well tolerated in rodent and non-human primate animal models.

For research use only. We do not sell to patients.

HMBD-002

HMBD-002 Chemical Structure

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Description

HMBD-002 is an Fc-independent, non-depleting IgG4 subclass antibody that targets VISTA and VSIG3. It is widely used in research related to various solid tumors, including colon cancer, triple-negative breast cancer, and non-small cell lung cancer. HMBD-002 blocks the interactions of VISTA with VSIG3 and LRIG1, relieves immunosuppression without depleting VISTA-positive cells, activates the cytotoxic program of CD8+ T cells, and drives the type I interferon signaling pathway. HMBD-002 reprograms tumor-associated macrophages to the M1 phenotype, reduces tumor infiltration of inhibitory myeloid cells, thereby significantly inhibiting tumor growth and improving survival. HMBD-002 is well tolerated in rodent and non-human primate animal models[1][2][3][4].

Isotype

Human IgG4 kappa

Recommend Isotype Controls
Species Reactivity

Human

In Vitro

HMBD-002 (1-10 μg/mL) reverses VSIG3-mediated suppression of activated human PBMCs, with greater activity observed at 10 μg/mL compared to 1 μg/mL in a 1:2 VSIG3-Fc to αCD3 coating ratio assay[1].
HMBD-002 (1-30 μg/mL) enhances immune activation in human PBMC MLRs, significantly increasing TNF-α and IFN-γ production at a concentration of 30 μg/mL[1].
HMBD-002 inhibits the interaction between recombinant VISTA and LRIG1 proteins with an IC50 of 3.4 nM[3].
HMBD-002 (1-10 µg/mL; 24 hours at 37°C) reverses VSIG3-mediated suppression of IFN-γ secretion from anti-CD3-activated human PBMCs, with significant restoration of IFN-γ levels at 1 µg/mL and 10 µg/mL[3].
HMBD-002 (1-30 µg/mL; 96 hours at 37°C) polarizes the immune milieu toward a proinflammatory Th1/Th17 response in human allogenic MLRs, inducing significant dose-dependent increases in IFN-γ and TNF-α and enriching proinflammatory signaling pathways at 1 µg/mL, 10 µg/mL, and 30 µg/mL[3].

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

ELISA Assay[3]

Cell Line: human PBMCs
Concentration: 1-10 µg/mL
Incubation Time: 24 hours
Result: Reversed VSIG3-mediated suppression of IFN-γ secretion, with significant restoration of IFN-γ levels at 1 µg/mL and 10 µg/mL.
In Vivo

HMBD-002 (25 mg/kg; i.p.; biweekly) delivers 84% tumor growth inhibition in a BALB/c mouse CT26 colorectal cancer model, remodels the TME to reduce suppressive myeloid cells and increase activated immune cells, and enhances antigen-specific cytotoxic T cell activity[3].
HMBD-002 (50 µg; intratumorally; on days 7, 9, 12, 14, 16 post implantation) achieves 53% tumor growth inhibition in a BALB/c mouse orthotopic 4T1 breast cancer model[3].
HMBD-002 (25 mg/kg; i.p.; biweekly) produces 65% tumor growth inhibition in a humanized HiMouse HCT15 colorectal cancer model[3].
HMBD-002 (25 mg/kg; i.p.; biweekly) delivers 62% tumor growth inhibition in a humanized HiMouse A549 lung cancer model[3].
HMBD-002 monotherapy activates the immune system (inducing up to 4-fold increases in serum IL-2, IL-17, and IFNγ) and achieves >60% tumor growth inhibition after 15 days in a CT26 syngeneic colon cancer BALB/C mouse model, with no observable toxicity[4].

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

Animal Model: BALB/c mice (female; subcutaneously implanted with CT26 cells)[3]
Dosage: 25 mg/kg
Administration: i.p.; biweekly
Result: Demonstrated 84% tumor growth inhibition (TGI) compared with vehicle.
Increased the percentage of CD11b+ MHCII+ antigen presenting cells, CD11b+ F4/80+ macrophages, and CD11C+ dendritic cells in the tumor microenvironment (TME).
Decreased the frequency of total myeloid-derived suppressor cells (CD11b+ GR1+ MHCII−) in the TME.
Showed significantly higher lysis of CT26 cells by tumor-infiltrating lymphocytes (TILs) in an ex vivo antigen recall assay.
Induced significantly higher IFN-γ levels in T cells when co-cultured with CT26 cells.
Gene ID

64115  [NCBI]

Accession
Target

B7-H5/VISTA

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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Product Name:
HMBD-002
Cat. No.:
HY-P992369
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