Lirilumab (Biosimilar Reference Antibody) (KIRD2)
Lirilumab (Biosimilar Reference Antibody) (KIRD2)
Lirilumab (Biosimilar Reference Antibody) (KIRD2)-RA0442-Oursmab determined by SDS-PAGE. The purity of the protein is greater than 98%.
ELISA plate pre-coated Antigen protein, can bind Lirilumab (Biosimilar Reference Antibody) (KIRD2)-RA0442 in a linear range of 15.63–31 ng/mL.
Lirilumab (Biosimilar Reference Antibody) (KIRD2)

Catalog: 

RA0442

Target

KIRD2

Isotype

IgG4 - kappa

Applications

ELISA;FC;Functional Assays;IF

Reactivities

Human

Size ($):

100 μg-50;1 mg-210;5 mg-500;10 mg-800;25 mg-1750;50 mg-3000;100 mg-4600

Data Sheet

Material Safety Data Sheet

Certificate of Analysis

Product Description

Lirilumab (also known as IPH-2102/BMS-986015) is a fully human monoclonal antibody that functions as an antagonist of killer cell immunoglobulin-like receptors (KIRs), specifically targeting the inhibitory receptors KIR2DL-1, -2, and -3 on natural killer (NK) cells and some T-cell subsets. By blocking these inhibitory KIRs, lirilumab prevents their interaction with their ligands (specific HLA-C allotypes) on tumor cells, thereby releasing the “brake” on NK cell activity. This aims to enhance NK cell-mediated killing of tumor cells, a mechanism known as “missing-self” recognition. It has been investigated clinically as an immuno-oncology agent, primarily in hematologic malignancies such as acute myeloid leukemia (AML) and multiple myeloma, often in combination with other therapies.

Synonyms

BMS-986015, IPH2102

CAS

1000676-41-4

Isotype

IgG4 - kappa

Host

Genetically human

Target

KIRD2

Reactivity

Human

Expression System

CHO

Applications

ELISA, FC, Functional Assays, IF; Recommended dilution: FC, IF:1:200

Purity

>98% by SDS-PAGE

Concentration

Bottled at the concentration indicated on the vial.

Buffer

0.01M PBS, pH 7.4, contains no stabilizers or preservatives.

Endotoxin

<1.0 EU/mg as determined by LAL method

Conjugation

Non-conjugated

Formulation

Liquid or Lyophilized powder Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.

Storage

store at -20°C or -80°C. Avoid repeated freeze.

Type

Antibody

Purposes

For research use only

References 1

Hanna GJ, et al. Neoadjuvant and Adjuvant Nivolumab and Lirilumab in Patients with Recurrent, Resectable Squamous Cell Carcinoma of the Head and Neck. Clin Cancer Res. 2022 Feb 1;28(3):468-478.

References 2

Hanna GJ, et al. Neoadjuvant and Adjuvant Nivolumab and Lirilumab in Patients with Recurrent, Resectable Squamous Cell Carcinoma of the Head and Neck. Clin Cancer Res. 2022 Feb 1;28(3):468-478.

References 3

References 4

References 5

Product Citations 1

Product Citations 2

https://pubmed.ncbi.nlm.nih.gov/34667025/
https://pubmed.ncbi.nlm.nih.gov/24326534/

Target Description

Synonyms

(killer cell Immunoglobulin-like receptors from KIRD2 subgroup, including KIR2DL1 (nkat1/CD158A), KIR2DL2 (nkat6/CD158B1), KIR2DL3 (nkat2/CD158B2), KIR2DS1 (CD158H) and KIR2DS2 (nkat5/CD158J)

Biology Area

Immunology;Immune Checkpoint;CD Markers

Function

Inhibitory killer cell immunoglobulin-like receptors (KIRs), including KIR2DL-1, -2, and -3, are transmembrane receptors expressed on the surface of NK cells and some T cells. They recognize specific HLA class I molecules (primarily HLA-C allotypes) on target cells. Under normal conditions, this interaction delivers an inhibitory signal that prevents NK cells from attacking healthy “self” cells that express adequate levels of HLA class I. Many tumors downregulate HLA class I expression to evade T-cell recognition, but this can make them vulnerable to NK cell attack—a process normally kept in check by residual HLA-KIR interactions. Blocking inhibitory KIRs with antibodies like lirilumab aims to overcome this checkpoint and unleash NK cell cytotoxicity against tumors, particularly those with diminished HLA class I expression.

Additional Articles 1

Additional Articles 2

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